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+%%
+%% This is file `carom.sty',
+%% generated with the docstrip utility.
+%%
+%% The original source files were:
+%%
+%% carom.dtx (with options: `carom')
+%%
+%% This is a generated file.
+%%
+%% Copyright 1996, 1988, 2000, 2001, 2002, 2004, 2010 by Shinsaku Fujita
+%% all rights reserved.
+%% This style file is created for drawing chemical structural formulas
+%% This style file is to be contained in the ``xymtex'' directory which
+%% is an input directory for TeX.
+%%
+%% This file is part of the XyMTeX system.
+%% =======================================
+%%
+%% Old Versions:
+%% Version 1.01 Released on August 16, 1996
+%% Version 1.02 Released on October 31, 1998
+%% Version 2.00 Released on December 25, 1998
+%% Version 2.00a Released on June 14, 2000
+%% Version 2.01 Released on June 20, 2001 (private version)
+%% Version 3.00 Released on April 30, 2002
+%% Version 4.00 Released on May 30, 2002 (private version)
+%% Version 4.01 Released on August 30, 2004
+%%
+%% The Present Version:
+%% Version 5.00 Released on October 01, 2010
+%%
+%% This work may be distributed and/or modified under the
+%% conditions of the LaTeX Project Public License, either version 1.3
+%% of this license or (at your option) any later version.
+%% The latest version of this license is in
+%% http://www.latex-project.org/lppl.txt
+%% and version 1.3 or later is part of all distributions of LaTeX
+%% version 2005/12/01 or later.
+%%
+%% This work has the LPPL maintenance status `maintained'.
+%% The Current Maintainer of this work is Shinsaku Fujita.
+%%
+%% This work consists of the files carom.dtx and carom.ins
+%% and the derived file carom.sty.
+%%
+%% =======================================
+%%
+%% File: carom.dtx
+%% \CharacterTable
+%% {Upper-case \A\B\C\D\E\F\G\H\I\J\K\L\M\N\O\P\Q\R\S\T\U\V\W\X\Y\Z
+%% Lower-case \a\b\c\d\e\f\g\h\i\j\k\l\m\n\o\p\q\r\s\t\u\v\w\x\y\z
+%% Digits \0\1\2\3\4\5\6\7\8\9
+%% Exclamation \! Double quote \" Hash (number) \#
+%% Dollar \$ Percent \% Ampersand \&
+%% Acute accent \' Left paren \( Right paren \)
+%% Asterisk \* Plus \+ Comma \,
+%% Minus \- Point \. Solidus \/
+%% Colon \: Semicolon \; Less than \<
+%% Equals \= Greater than \> Question mark \?
+%% Commercial at \@ Left bracket \[ Backslash \\
+%% Right bracket \] Circumflex \^ Underscore \_
+%% Grave accent \` Left brace \{ Vertical bar \|
+%% Right brace \} Tilde \~}
+\typeout{XyMTeX for Drawing Chemical Structural Formulas. Version 5.00}
+\typeout{ -- Released October 01, 2010 by Shinsaku Fujita}
+\def\j@urnalname{carom}
+\def\versi@ndate{October 01, 2010}
+\def\versi@nno{ver5.00}
+\def\copyrighth@lder{SF} % Shinsaku Fujita
+\typeout{XyMTeX Macro File `\j@urnalname' (\versi@nno) <\versi@ndate>%
+\space[\copyrighth@lder]}
+\@ifundefined{setsixringv}{\input chemstr.sty\relax}{}
+\@ifundefined{decaheterov}{\input hetarom.sty\relax}{}
+\@ifundefined{decaheteroh}{\input hetaromh.sty\relax}{}
+\unitlength=0.1pt
+\def\cyclohexanev{\@ifnextchar[{\@cyclohexanev[@}{\@cyclohexanev[@]}}
+\def\@cyclohexanev[#1]#2{\sixheterov[#1]{}{#2}}
+\def\cyclohexaneh{\@ifnextchar[{\@cyclohexaneh[@}{\@cyclohexaneh[@]}}
+\def\@cyclohexaneh[#1]#2{\sixheteroh[#1]{}{#2}}
+\def\bzdrv{\@ifnextchar[{\@bzdrv}{\@bzdrv[r]}}
+\def\@bzdrv[#1]#2{%
+\iforigpt \typeout{command `bzdrv' is based on `cyclohexanev'.}\fi%
+\expandafter\twoCH@R#1//%
+\if\@tmpa r% right-handed set of double bonds
+ \ifx\@tmpb\empty
+ \cyclohexanev[bdf]{#2}%
+ \fi
+\else\if\@tmpa l%left-handed set of double bonds
+ \ifx\@tmpb\empty
+ \cyclohexanev[ace]{#2}%
+ \fi
+\else\if\@tmpa c%aromatic circle
+ \ifx\@tmpb\empty
+ \cyclohexanev[A]{#2}%
+ \fi
+\else\if\@tmpa p%p-quinone
+ \if\@tmpb a% (A)
+ \cyclohexanev[be]{#2}%
+ \else\ifx\@tmpb\empty% (A)
+ \cyclohexanev[be]{#2}%
+ \else\if\@tmpb b% (B)
+ \cyclohexanev[cf]{#2}%
+ \else\if\@tmpb c% (C)
+ \cyclohexanev[ad]{#2}%
+ \fi\fi\fi\fi%
+\else\if\@tmpa o%o-quinone
+ \if\@tmpb a% (A)%
+ \cyclohexanev[ce]{#2}%
+ \else\ifx\@tmpb\empty% (A)
+ \cyclohexanev[ce]{#2}%
+ \else\if\@tmpb b%o-quinone (B)
+ \cyclohexanev[df]{#2}%
+ \else\if\@tmpb c%o-quinone (C)
+ \cyclohexanev[ae]{#2}%
+ \else\if\@tmpb d%o-quinone (D)
+ \cyclohexanev[bf]{#2}%
+ \else\if\@tmpb e%o-quinone (E)
+ \cyclohexanev[ac]{#2}%
+ \else\if\@tmpb f%o-quinone (F)
+ \cyclohexanev[bd]{#2}%
+ \fi\fi\fi\fi\fi\fi\fi%
+\else% added 1998/11/15 by S. Fujita
+ \cyclohexanev[@#1]{#2}%
+\fi\fi\fi\fi\fi%
+}% %end of \bzdrv macro
+\let\benzenev=\bzdrv
+\def\bzdrh{\@ifnextchar[{\@bzdrh}{\@bzdrh[r]}}
+\def\@bzdrh[#1]#2{%
+\iforigpt \typeout{command `bzdrh' is based on `cyclohexaneh'.}\fi%
+\expandafter\twoCH@R#1//%
+\if\@tmpa r% right-handed set of double bonds
+ \cyclohexaneh[bdf]{#2}%
+\else\if\@tmpa l%left-handed set of double bonds
+ \cyclohexaneh[ace]{#2}%
+\else\if\@tmpa c%aromatic circle
+ \cyclohexaneh[A]{#2}%
+\else\if\@tmpa p%p-quinone
+ \if\@tmpb a% (A)
+ \cyclohexaneh[be]{#2}%
+ \else\ifx\@tmpb\empty% (A)
+ \cyclohexaneh[be]{#2}%
+ \else\if\@tmpb b% (B)
+ \cyclohexaneh[cf]{#2}%
+ \else\if\@tmpb c% (C)
+ \cyclohexaneh[ad]{#2}%
+ \fi\fi\fi\fi%
+\else\if\@tmpa o%o-quinone
+ \if\@tmpb a% (A)%
+ \cyclohexaneh[ce]{#2}%
+ \else\ifx\@tmpb\empty% (A)
+ \cyclohexaneh[ce]{#2}%
+ \else\if\@tmpb b%o-quinone (B)
+ \cyclohexaneh[df]{#2}%
+ \else\if\@tmpb c%o-quinone (C)
+ \cyclohexaneh[ae]{#2}%
+ \else\if\@tmpb d%o-quinone (D)
+ \cyclohexaneh[bf]{#2}%
+ \else\if\@tmpb e%o-quinone (E)
+ \cyclohexaneh[ac]{#2}%
+ \else\if\@tmpb f%o-quinone (F)
+ \cyclohexaneh[bd]{#2}%
+ \fi\fi\fi\fi\fi\fi\fi%
+\else% added 1998/11/15 by S. Fujita
+ \cyclohexaneh[@#1]{#2}%
+\fi\fi\fi\fi\fi%
+}% %end of \bzdrh macro
+\let\benzeneh=\bzdrh
+\def\decalinev{\@ifnextchar[{\@decalinev[@}{\@decalinev[@]}}
+\def\@decalinev[#1]#2{%
+\iforigpt \typeout{command `decalinev' is based on `decaheterov'.}\fi%
+\decaheterov[#1]{}{#2}}
+\def\decalinevb{\@ifnextchar[{\@decalinevb[@}{\@decalinevb[@]}}
+\def\@decalinevb[#1]#2{%
+\iforigpt \typeout{command `decalinevb' is based on `decaheterovb'.}\fi%
+\decaheterovb[#1]{}{#2}}
+\def\decalinevt{\@ifnextchar[{\@decalinevt[@}{\@decalinevt[@]}}
+\def\@decalinevt[#1]#2{%
+\iforigpt \typeout{command `decalinevt' is based on `decaheterovt'.}\fi%
+\decaheterovt[#1]{}{#2}}
+\def\decalineh{\@ifnextchar[{\@decalineh[@}{\@decalineh[@]}}
+\def\@decalineh[#1]#2{%
+\iforigpt \typeout{command `decalineh' is based on `decaheteroh'.}\fi%
+\decaheteroh[#1]{}{#2}}
+\def\naphdrv{\@ifnextchar[{\@naphdrv}{\@naphdrv[r]}}
+\def\@naphdrv[#1]#2{%
+\iforigpt \typeout{command `naphdrv' is based on `decalinev'.}\fi%
+ \expandafter\threech@r#1{}{}%
+\if\@tmpa r% right-handed set of double bonds
+ \decalinev[acfhk]{#2}%
+\else\if\@tmpa A%aromatic circle
+ \decalinev[AB]{#2}%
+\else\if\@tmpa p%p-quinone
+ \if\@tmpb a% (A)
+ \decalinev[bfhk]{#2}%
+ \else\ifx\@tmpb\empty% (A)
+ \decalinev[bfhk]{#2}%
+ \else\if\@tmpb b% (B)
+ \decalinev[acgk]{#2}%
+ \fi\fi\fi%
+\else%
+ \if\@tmpa o%o-quinone
+ \if\@tmpb a% (A)
+ \decalinev[cfhk]{#2}%
+ \else\ifx\@tmpb\empty% (A)
+ \decalinev[cfhk]{#2}%
+ \else\if\@tmpb b%o-quinone (B)
+ \decalinev[dfhj]{#2}%
+ \else\if\@tmpb c%o-quinone (C)
+ \decalinev[afhk]{#2}%
+ \else\if\@tmpb d%o-quinone (D)
+ \decalinev[achk]{#2}%
+ \else\if\@tmpb e%o-quinone (E)
+ \decalinev[acei]{#2}%
+ \else\if\@tmpb f%o-quinone (F)
+ \decalinev[acfk]{#2}%
+ \fi\fi\fi\fi\fi\fi%
+ \fi%
+%%%
+\else\if\@tmpa q%various quinone
+ \if\@tmpb a% (A)2,6-type
+ \decalinev[cehj]{#2}%
+ \else\ifx\@tmpb\empty% (A)2,6-type
+ \decalinev[cehj]{#2}%
+ \else\if\@tmpb b%2,6-quinone (B)
+ \decalinev[adfi]{#2}%
+ \else\if\@tmpb c%1,5-quinone (C)
+ \decalinev[bdgi]{#2}%
+ \else\if\@tmpb d%1,5-quinone (D)
+ \decalinev[begj]{#2}%
+ \else\if\@tmpb e%1,7-quinone (E)
+ \decalinev[bdfi]{#2}%
+ \else\if\@tmpb f%1,7-quinone (F)
+ \decalinev[cegj]{#2}%
+ \else\if\@tmpb g%1,7-quinone (G)
+ \decalinev[behj]{#2}%
+ \else\if\@tmpb h%1,7-quinone (H)
+ \decalinev[adgi]{#2}%
+ \fi\fi\fi\fi\fi\fi\fi\fi\fi%
+\else\if\@tmpa P%quinone having 4 carbonyl groups
+ \if\@tmpb a% (A)1,4,5,8-type
+ \decalinev[bgk]{#2}%
+ \else\ifx\@tmpb\empty% (A)1,4,5,8-type
+ \decalinev[bgk]{#2}%
+ \else\if\@tmpb b% (B)1,2,5,8-type
+ \decalinev[cgk]{#2}%
+ \fi\fi\fi%
+\else\if\@tmpa Q%1,2,3,4
+ \decalinev[fhk]{#2}%
+\else\if\@tmpa O%quinone having 4 carbonyl groups
+ \if\@tmpb a% (A)1,2,5,6-type
+ \decalinev[chk]{#2}%
+ \else\ifx\@tmpb\empty% (A)1,2,5,6-type
+ \decalinev[chk]{#2}%
+ \else\if\@tmpb b% (B)1,2,7,8-type
+ \decalinev[cfk]{#2}%
+ \else\if\@tmpb c% (C)1,2,3,5-type
+ \decalinev[dgi]{#2}%
+ \else\if\@tmpb d% (D)1,2,3,7-type
+ \decalinev[dfi]{#2}%
+ \fi\fi\fi\fi\fi%
+\else% added 1998/11/23 by S. Fujita
+ \decalinev[@#1]{#2}%
+\fi\fi\fi\fi\fi\fi\fi\fi%
+}% %end of \naphdrv macro
+\let\naphthalenev=\naphdrv
+\def\naphdrvb{\@ifnextchar[{\@naphdrvb}{\@naphdrvb[r]}}
+\def\@naphdrvb[#1]#2{%
+\iforigpt \typeout{command `naphdrvb' is based on `decalinevb'.}\fi%
+ \expandafter\threech@r#1{}{}%
+\if\@tmpa r% right-handed set of double bonds
+ \decalinevb[acfhk]{#2}%
+\else\if\@tmpa A%aromatic circle
+ \decalinevb[AB]{#2}%
+\else\if\@tmpa p%p-quinone
+ \if\@tmpb a% (A)
+ \decalinevb[bfhk]{#2}%
+ \else\ifx\@tmpb\empty% (A)
+ \decalinevb[bfhk]{#2}%
+ \else\if\@tmpb b% (B)
+ \decalinevb[acgk]{#2}%
+ \fi\fi\fi%
+\else%
+ \if\@tmpa o%o-quinone
+ \if\@tmpb a% (A)
+ \decalinevb[cfhk]{#2}%
+ \else\ifx\@tmpb\empty% (A)
+ \decalinevb[cfhk]{#2}%
+ \else\if\@tmpb b%o-quinone (B)
+ \decalinevb[dfhj]{#2}%
+ \else\if\@tmpb c%o-quinone (C)
+ \decalinevb[afhk]{#2}%
+ \else\if\@tmpb d%o-quinone (D)
+ \decalinevb[achk]{#2}%
+ \else\if\@tmpb e%o-quinone (E)
+ \decalinevb[acei]{#2}%
+ \else\if\@tmpb f%o-quinone (F)
+ \decalinevb[acfk]{#2}%
+ \fi\fi\fi\fi\fi\fi%
+ \fi%
+%%%
+\else\if\@tmpa q%various quinone
+ \if\@tmpb a% (A)2,6-type
+ \decalinevb[cehj]{#2}%
+ \else\ifx\@tmpb\empty% (A)2,6-type
+ \decalinevb[cehj]{#2}%
+ \else\if\@tmpb b%2,6-quinone (B)
+ \decalinevb[adfi]{#2}%
+ \else\if\@tmpb c%1,5-quinone (C)
+ \decalinevb[bdgi]{#2}%
+ \else\if\@tmpb d%1,5-quinone (D)
+ \decalinevb[begj]{#2}%
+ \else\if\@tmpb e%1,7-quinone (E)
+ \decalinevb[bdfi]{#2}%
+ \else\if\@tmpb f%1,7-quinone (F)
+ \decalinevb[cegj]{#2}%
+ \else\if\@tmpb g%1,7-quinone (G)
+ \decalinevb[behj]{#2}%
+ \else\if\@tmpb h%1,7-quinone (H)
+ \decalinevb[adgi]{#2}%
+ \fi\fi\fi\fi\fi\fi\fi\fi\fi%
+\else\if\@tmpa P%quinone having 4 carbonyl groups
+ \if\@tmpb a% (A)1,4,5,8-type
+ \decalinevb[bgk]{#2}%
+ \else\ifx\@tmpb\empty% (A)1,4,5,8-type
+ \decalinevb[bgk]{#2}%
+ \else\if\@tmpb b% (B)1,2,5,8-type
+ \decalinevb[cgk]{#2}%
+ \fi\fi\fi%
+\else\if\@tmpa Q%1,2,3,4
+ \decalinevb[fhk]{#2}%
+\else\if\@tmpa O%quinone having 4 carbonyl groups
+ \if\@tmpb a% (A)1,2,5,6-type
+ \decalinevb[chk]{#2}%
+ \else\ifx\@tmpb\empty% (A)1,2,5,6-type
+ \decalinevb[chk]{#2}%
+ \else\if\@tmpb b% (B)1,2,7,8-type
+ \decalinevb[cfk]{#2}%
+ \else\if\@tmpb c% (C)1,2,3,5-type
+ \decalinevb[dgi]{#2}%
+ \else\if\@tmpb d% (D)1,2,3,7-type
+ \decalinevb[dfi]{#2}%
+ \fi\fi\fi\fi\fi%
+\else% added 1998/11/23 by S. Fujita
+ \decalinevb[@#1]{#2}%
+\fi\fi\fi\fi\fi\fi\fi\fi%
+}% %end of \naphdrvb macro
+\let\naphthalenevb=\naphdrvb
+\def\naphdrvt{\@ifnextchar[{\@naphdrvt}{\@naphdrvt[r]}}
+\def\@naphdrvt[#1]#2{%
+\iforigpt \typeout{command `naphdrvt' is based on `decalinevt'.}\fi%
+ \expandafter\threech@r#1{}{}%
+\if\@tmpa r% right-handed set of double bonds
+ \decalinevt[acfhk]{#2}%
+\else\if\@tmpa A%aromatic circle
+ \decalinevt[AB]{#2}%
+\else\if\@tmpa p%p-quinone
+ \if\@tmpb a% (A)
+ \decalinevt[bfhk]{#2}%
+ \else\ifx\@tmpb\empty% (A)
+ \decalinevt[bfhk]{#2}%
+ \else\if\@tmpb b% (B)
+ \decalinevt[acgk]{#2}%
+ \fi\fi\fi%
+\else%
+ \if\@tmpa o%o-quinone
+ \if\@tmpb a% (A)
+ \decalinevt[cfhk]{#2}%
+ \else\ifx\@tmpb\empty% (A)
+ \decalinevt[cfhk]{#2}%
+ \else\if\@tmpb b%o-quinone (B)
+ \decalinevt[dfhj]{#2}%
+ \else\if\@tmpb c%o-quinone (C)
+ \decalinevt[afhk]{#2}%
+ \else\if\@tmpb d%o-quinone (D)
+ \decalinevt[achk]{#2}%
+ \else\if\@tmpb e%o-quinone (E)
+ \decalinevt[acei]{#2}%
+ \else\if\@tmpb f%o-quinone (F)
+ \decalinevt[acfk]{#2}%
+ \fi\fi\fi\fi\fi\fi%
+ \fi%
+%%%
+\else\if\@tmpa q%various quinone
+ \if\@tmpb a% (A)2,6-type
+ \decalinevt[cehj]{#2}%
+ \else\ifx\@tmpb\empty% (A)2,6-type
+ \decalinevt[cehj]{#2}%
+ \else\if\@tmpb b%2,6-quinone (B)
+ \decalinevt[adfi]{#2}%
+ \else\if\@tmpb c%1,5-quinone (C)
+ \decalinevt[bdgi]{#2}%
+ \else\if\@tmpb d%1,5-quinone (D)
+ \decalinevt[begj]{#2}%
+ \else\if\@tmpb e%1,7-quinone (E)
+ \decalinevt[bdfi]{#2}%
+ \else\if\@tmpb f%1,7-quinone (F)
+ \decalinevt[cegj]{#2}%
+ \else\if\@tmpb g%1,7-quinone (G)
+ \decalinevt[behj]{#2}%
+ \else\if\@tmpb h%1,7-quinone (H)
+ \decalinevt[adgi]{#2}%
+ \fi\fi\fi\fi\fi\fi\fi\fi\fi%
+\else\if\@tmpa P%quinone having 4 carbonyl groups
+ \if\@tmpb a% (A)1,4,5,8-type
+ \decalinevt[bgk]{#2}%
+ \else\ifx\@tmpb\empty% (A)1,4,5,8-type
+ \decalinevt[bgk]{#2}%
+ \else\if\@tmpb b% (B)1,2,5,8-type
+ \decalinevt[cgk]{#2}%
+ \fi\fi\fi%
+\else\if\@tmpa Q%1,2,3,4
+ \decalinevt[fhk]{#2}%
+\else\if\@tmpa O%quinone having 4 carbonyl groups
+ \if\@tmpb a% (A)1,2,5,6-type
+ \decalinevt[chk]{#2}%
+ \else\ifx\@tmpb\empty% (A)1,2,5,6-type
+ \decalinevt[chk]{#2}%
+ \else\if\@tmpb b% (B)1,2,7,8-type
+ \decalinevt[cfk]{#2}%
+ \else\if\@tmpb c% (C)1,2,3,5-type
+ \decalinevt[dgi]{#2}%
+ \else\if\@tmpb d% (D)1,2,3,7-type
+ \decalinevt[dfi]{#2}%
+ \fi\fi\fi\fi\fi%
+\else% added 1998/11/23 by S. Fujita
+ \decalinevt[@#1]{#2}%
+\fi\fi\fi\fi\fi\fi\fi\fi%
+}% %end of \naphdrvt macro
+\let\naphthalenevt=\naphdrvt
+\def\naphdrh{\@ifnextchar[{\@naphdrh}{\@naphdrh[r]}}
+\def\@naphdrh[#1]#2{%
+\iforigpt \typeout{command `nathdrh' is based on `decalineh'.}\fi%
+ \expandafter\threech@r#1{}{}%
+\if\@tmpa r% right-handed set of double bonds
+ \decalineh[acfhk]{#2}%
+\else\if\@tmpa A%aromatic circle
+ \decalineh[AB]{#2}%
+\else\if\@tmpa p%p-quinone
+ \if\@tmpb a% (A)
+ \decalineh[bfhk]{#2}%
+ \else\ifx\@tmpb\empty% (A)
+ \decalineh[bfhk]{#2}%
+ \else\if\@tmpb b% (B)
+ \decalineh[acgk]{#2}%
+ \fi\fi\fi%
+\else%
+ \if\@tmpa o%o-quinone
+ \if\@tmpb a% (A)
+ \decalineh[cfhk]{#2}%
+ \else\ifx\@tmpb\empty% (A)
+ \decalineh[cfhk]{#2}%
+ \else\if\@tmpb b%o-quinone (B)
+ \decalineh[dfhj]{#2}%
+ \else\if\@tmpb c%o-quinone (C)
+ \decalineh[afhk]{#2}%
+ \else\if\@tmpb d%o-quinone (D)
+ \decalineh[achk]{#2}%
+ \else\if\@tmpb e%o-quinone (E)
+ \decalineh[acei]{#2}%
+ \else\if\@tmpb f%o-quinone (F)
+ \decalineh[acfk]{#2}%
+ \fi\fi\fi\fi\fi\fi%
+ \fi%
+\else\if\@tmpa q%various quinone
+ \if\@tmpb a% (A)2,6-type
+ \decalineh[cehj]{#2}%
+ \else\ifx\@tmpb\empty% (A)2,6-type
+ \decalineh[cehj]{#2}%
+ \else\if\@tmpb b%2,6-quinone (B)
+ \decalineh[adfi]{#2}%
+ \else\if\@tmpb c%1,5-quinone (C)
+ \decalineh[bdgi]{#2}%
+ \else\if\@tmpb d%1,5-quinone (D)
+ \decalineh[begj]{#2}%
+ \else\if\@tmpb e%1,7-quinone (E)
+ \decalineh[bdfi]{#2}%
+ \else\if\@tmpb f%1,7-quinone (F)
+ \decalineh[cegj]{#2}%
+ \else\if\@tmpb g%1,7-quinone (G)
+ \decalineh[behj]{#2}%
+ \else\if\@tmpb h%1,7-quinone (H)
+ \decalineh[adgi]{#2}%
+ \fi\fi\fi\fi\fi\fi\fi\fi\fi%
+\else\if\@tmpa P%quinone having 4 carbonyl groups
+ \if\@tmpb a% (A)1,4,5,8-type
+ \decalineh[bgk]{#2}%
+ \else\ifx\@tmpb\empty% (A)1,4,5,8-type
+ \decalineh[bgk]{#2}%
+ \else\if\@tmpb b% (B)1,2,5,8-type
+ \decalineh[cgk]{#2}%
+ \fi\fi\fi%
+\else\if\@tmpa Q%1,2,3,4
+ \decalineh[fhk]{#2}%
+\else\if\@tmpa O%quinone having 4 carbonyl groups
+ \if\@tmpb a% (A)1,2,5,6-type
+ \decalineh[chk]{#2}%
+ \else\ifx\@tmpb\empty% (A)1,2,5,6-type
+ \decalineh[chk]{#2}%
+ \else\if\@tmpb b% (B)1,2,7,8-type
+ \decalineh[cfk]{#2}%
+ \else\if\@tmpb c% (C)1,2,3,5-type
+ \decalineh[dgi]{#2}%
+ \else\if\@tmpb d% (D)1,2,3,7-type
+ \decalineh[dfi]{#2}%
+ \fi\fi\fi\fi\fi%
+\else% added 1998/11/23 by S. Fujita
+ \decalineh[@#1]{#2}%
+\fi\fi\fi\fi\fi\fi\fi\fi%
+}% %end of \naphdrh macro
+\let\naphthaleneh=\naphdrh
+\def\tetralinev{\@ifnextchar[{\@tetralinev}{\@tetralinev[r]}}
+\def\@tetralinev[#1]#2{%
+ \iforigpt \typeout{command `tetralinev' is based on `decalinev'.}\fi%
+ \expandafter\threech@r#1{}{}%
+ \if\@tmpa r% right-handed set of double bonds
+ \decalinev[fhk]{#2}%
+ \else\if\@tmpa A%aromatic circle
+ \decalinev[A]{#2}%
+ \else\if\@tmpa e%inner double bond
+ \if\@tmpb a% (A)%
+ \decalinev[afhk]{#2}%
+ \else\ifx\@tmpb\empty% (A)
+ \decalinev[afhk]{#2}%
+ \else\if\@tmpb b% (B)
+ \decalinev[bfhk]{#2}%
+ \else\if\@tmpb c% (C)
+ \decalinev[cfhk]{#2}%
+ \fi\fi\fi\fi%
+ \else%1998/11/23 by Shinsaku Fujita
+ \decalinev[@#1]{#2}%
+ \fi\fi\fi%
+}% %end of \tetralinev macro
+\def\tetralinevb{\@ifnextchar[{\@tetralinevb}{\@tetralinevb[r]}}
+\def\@tetralinevb[#1]#2{%
+ \iforigpt \typeout{command `tetralinevb' is based on `decalinevb'.}\fi%
+ \expandafter\threech@r#1{}{}%
+ \if\@tmpa r% right-handed set of double bonds
+ \decalinevb[fhK]{#2}% %[fhK] in place of [fhk]
+ \else\if\@tmpa A%aromatic circle
+ \decalinevb[A]{#2}%
+ \else\if\@tmpa e%inner double bond
+ \if\@tmpb a% (A)%
+ \decalinevb[afhK]{#2}%
+ \else\ifx\@tmpb\empty% (A)
+ \decalinevb[afhK]{#2}%
+ \else\if\@tmpb b% (B)
+ \decalinevb[bfhK]{#2}%
+ \else\if\@tmpb c% (C)
+ \decalinevb[cfhK]{#2}%
+ \fi\fi\fi\fi%
+ \else%1998/11/23 by Shinsaku Fujita
+ \decalinevb[@#1]{#2}%
+ \fi\fi\fi%
+}% %end of \tetralinevb macro
+\def\tetralinevt{\@ifnextchar[{\@tetralinevt}{\@tetralinevt[r]}}
+\def\@tetralinevt[#1]#2{%
+ \iforigpt \typeout{command `tetralinevt' is based on `decalinevt'.}\fi%
+ \expandafter\threech@r#1{}{}%
+ \if\@tmpa r% right-handed set of double bonds
+ \decalinevt[fhk]{#2}%
+ \else\if\@tmpa A%aromatic circle
+ \decalinevt[A]{#2}%
+ \else\if\@tmpa e%inner double bond
+ \if\@tmpb a% (A)%
+ \decalinevt[afhk]{#2}%
+ \else\ifx\@tmpb\empty% (A)
+ \decalinevt[afhk]{#2}%
+ \else\if\@tmpb b% (B)
+ \decalinevt[bfhk]{#2}%
+ \else\if\@tmpb c% (C)
+ \decalinevt[cfhk]{#2}%
+ \fi\fi\fi\fi%
+ \else%1998/11/23 by Shinsaku Fujita
+ \decalinevt[@#1]{#2}%
+ \fi\fi\fi%
+}% %end of \tetralinevt macro
+\def\tetralineh{\@ifnextchar[{\@tetralineh}{\@tetralineh[r]}}
+\def\@tetralineh[#1]#2{%
+ \iforigpt \typeout{command `tetralineh' is based on `decalineh'.}\fi%
+ \expandafter\threech@r#1{}{}%
+ \if\@tmpa r% right-handed set of double bonds
+ \decalineh[fhk]{#2}%
+ \else\if\@tmpa A%aromatic circle
+ \decalineh[A]{#2}%
+ \else\if\@tmpa e%inner double bond
+ \if\@tmpb a% (A)%
+ \decalineh[afhk]{#2}%
+ \else\ifx\@tmpb\empty% (A)
+ \decalineh[afhk]{#2}%
+ \else\if\@tmpb b% (B)
+ \decalineh[bfhk]{#2}%
+ \else\if\@tmpb c% (C)
+ \decalineh[cfhk]{#2}%
+ \fi\fi\fi\fi%
+\else% added 1998/11/23 by S. Fujita
+ \decalineh[@#1]{#2}%
+ \fi\fi\fi%
+}% %end of \tetralineh macro
+\def\hanthracenev{\@ifnextchar[{\@hanthracenev[@}{\@hanthracenev[r]}}
+\def\@hanthracenev[#1]#2{%
+\@reset@ylsw\reset@@yl
+\ylposition{#2}{-7}{0}{2}{0}% %for 8 positions
+\if@ylsw \ifx\@@ylii\empty
+\def\@@ylii{0}\def\@@yli{0}\fi
+\else\ylposition{#2}{-1}{3}{7}{0}% for 5 to 7 positions
+\fi
+\if@ylsw\ifx\@@ylii\empty
+\def\@@ylii{0}\def\@@yli{0}\fi\else
+\ylposition{#2}{0}{0}{5}{0}% for 1 to 4 positions
+\fi
+\if@ylsw\ifx\@@ylii\empty
+\def\@@ylii{-684}\def\@@yli{0}\fi\else
+\ylposition{#2}{-8}{0}{2}{0}%for 9-position
+\fi
+\if@ylsw\ifx\@@ylii\empty
+\def\@@ylii{-342}\def\@@yli{0}\fi\else
+\ylposition{#2}{-6}{3}{5}{0}%for 10-position
+\fi
+\if@ylsw\ifx\@@ylii\empty
+\def\@@ylii{-342}\def\@@yli{0}\fi\else
+\ylfusedposition{#2}{-11}{-1}{1}{0}% for 9a and 4a
+\fi
+\if@ylsw\ifx\@@ylii\empty
+\def\@@ylii{-342}\def\@@yli{0}\fi\else
+\ylfusedposition{#2}{-12}{-1}{1}{0}% for 8a and 10a
+\fi
+\if@ylsw\ifx\@@ylii\empty
+\def\@@ylii{0}\def\@@yli{0}\fi\fi
+\if@ylsw
+ \yl@shiftii=\@ylii
+ \ifx\@@ylii\empty\else
+ \advance\yl@shiftii\@@ylii\fi
+ \yl@shifti=\@yli
+ \ifx\@@yli\empty\else
+ \advance\yl@shifti\@@yli\fi
+ \advance\yl@shiftii\yl@xdiff
+ \advance\yl@shifti\yl@ydiff
+ \begin{sfpicture}(0,0)(-\yl@shiftii,-\yl@shifti)%
+ \reset@yl@xydiff%1999/1/6 by S. Fujita
+\else
+ \begin{sfpicture}(1200,880)(-\shiftii,-\shifti)%
+ \origptoutput{hanthracenev}%
+\fi
+ \Put@Line(0,406)(-5,-3){171}% %bond 8-7
+ \Put@Line(0,406)(5,-3){171}% %bond 8-8a
+ \Put@Line(0,0)(-5,3){171}% %bond 5-6
+ \Put@Line(0,0)(5,3){171}% %bond 5-10a
+ \Put@Line(171,103)(0,1){200}% %bond 10a-8a
+ \Put@Line(-171,103)(0,1){200}% %bond 6-7
+ \Put@Line(342,406)(-5,-3){171}% %bond 9-8a
+ \Put@Line(342,406)(5,-3){171}% %bond 9-9a
+ \Put@Line(342,0)(-5,3){171}% %bond 10-10a
+ \Put@Line(342,0)(5,3){171}% %bond 10-4a
+ \Put@Line(513,103)(0,1){200}% %bond 4a-9a
+ %%%%
+ \Put@Line(684,406)(-5,-3){171}% %bond 1-9a 1-6
+ \Put@Line(684,406)(5,-3){171}% %bond 1-2 1-2
+ \Put@Line(855,103)(0,1){200}% %bond 3-2 3-2
+ \Put@Line(684,0)(5,3){171}% %bond 4-3 4-3
+ \Put@Line(684,0)(-5,3){171}% %bond 4-4a 4-5
+\@tfor\member:=#1\do{%
+\if\member r%no endcyclic double bonds
+\else\if\member a%
+ \Put@Line(690,364)(5,-3){126}% %double bond 1-2
+\else\if\member b%
+ \Put@Line(822,129)(0,1){148}% %double bond 3-2
+\else\if\member c%
+ \Put@Line(690,42)(5,3){126}% %double bond 4-3
+\else\if\member d%
+ \Put@Line(690,42)(-5,3){126}% %double bond 4-4a
+\else\if\member e%
+ \Put@Line(348,42)(5,3){126}% %double bond 10-4a
+\else\if\member f%
+ \Put@Line(348,42)(-5,3){126}% %double bond 10-10a
+\else\if\member g%
+ \Put@Line(6,42)(5,3){126}% %double bond 5-10a
+\else\if\member h%
+ \Put@Line(-6,42)(-5,3){126}% %double bond 5-6
+\else\if\member i%
+ \Put@Line(-138,129)(0,1){148}% %double bond 6-7
+\else\if\member j%
+ \Put@Line(-6,364)(-5,-3){126}% %double bond 8-7
+\else\if\member k%
+ \Put@Line(6,364)(5,-3){126}% %double bond 8-8a
+\else\if\member l%
+ \Put@Line(348,364)(-5,-3){126}% %double bond 9-8a
+\else\if\member m%
+ \Put@Line(348,364)(5,-3){126}% %double bond 9-9a
+\else\if\member n%
+ \Put@Line(690,364)(-5,-3){126}% %double bond 1-9a
+\else\if\member o%
+ \Put@Line(544,129)(0,1){148}% %double bond 4a-9a
+\else\if\member O%
+ \Put@Line(482,129)(0,1){148}% %double bond 4a-9a at the other ring
+\else\if\member p%
+ \Put@Line(138,129)(0,1){148}% %double bond 10a-8a
+\else\if\member P%
+ \Put@Line(204,129)(0,1){148}% %double bond 10a-8a at the other ring
+\else\if\member C%left aromatic circle
+ \Put@oCircle(0,203){240}% %circle
+\else\if\member B%right aromatic circle
+ \Put@oCircle(342,203){240}% %circle
+\else\if\member A%right aromatic circle
+ \Put@oCircle(684,203){240}% %circle
+\else
+ \expandafter\twoCH@R\member//%
+ \set@fusion@hanthrav
+\fi\fi\fi\fi\fi\fi\fi\fi\fi\fi\fi\fi\fi\fi\fi\fi\fi\fi\fi\fi\fi\fi}%
+\global\drawsamesubsttrue%2002/05/30 warning on
+\Put@Direct(0,0){\setsixringv{#2}{-7}{0}{2}{0}}% %for 8 positions
+\global\drawsamesubstfalse%2002/05/30 warning off
+\Put@Direct(0,0){\setsixringv{#2}{-1}{3}{7}{0}}% %for 5 to 7 positions
+\Put@Direct(684,0){\setsixringv{#2}{0}{0}{5}{0}}% %for 1 to 4 positions
+\Put@Direct(342,0){\setsixringv{#2}{-8}{0}{2}{0}}%for 9-position
+\Put@Direct(342,0){\setsixringv{#2}{-6}{3}{5}{0}}%for 10-position
+\Put@Direct(0,0){\setfusedbond{#2}{-12}{-1}{1}{0}}% for 8a and 10a
+\Put@Direct(342,0){\setfusedbond{#2}{-11}{-1}{1}{0}}% for 9a and 4a
+\end{sfpicture}}% %end of \hanthracenev macro%
+\def\anthracenev{\@ifnextchar[{\@anthracenev}{\@anthracenev[r]}}
+\def\@anthracenev[#1]#2{%
+ \iforigpt \typeout{command `anthracenev' is %
+ based on `hanthracenev'.}\fi%
+%% \expandafter\threech@r#1{}{}%error1998/11/23 by Shinsaku Fujita
+ \expandafter\twoCH@R#1//%
+ \if\@tmpa r% right-handed set of double bonds
+ \hanthracenev[acflhjo]{#2}%
+ \else\if\@tmpa l% left-handed set of double bonds
+ \hanthracenev[acehjmp]{#2}%
+ \else\if\@tmpa A%aromatic circle
+ \hanthracenev[ABC]{#2}%
+ \else\if\@tmpa p%9,10-quinone
+ \if\@tmpb a% (A)%
+ \hanthracenev[achjop]{#2}%
+ \else\ifx\@tmpb\empty% (A)
+ \hanthracenev[achjop]{#2}%
+ \else\if\@tmpb A% circle type
+ \hanthracenev[AC]{#2}%
+ \else
+ \hanthracenev[achjop]{#2}%
+ \fi\fi\fi%
+ \else\if\@tmpa o%o-quinone
+ \if\@tmpb a% (A)%
+ \hanthracenev[cfjhlo]{#2}%
+ \else\ifx\@tmpb\empty% (A)
+ \hanthracenev[cehjmp]{#2}%
+ \else\if\@tmpb b% (B)
+ \hanthracenev[dfhjln]{#2}%
+ \else\if\@tmpb c% (C)
+ \hanthracenev[aehjmp]{#2}%
+ \else\if\@tmpb A% cicle type
+ \hanthracenev[cBC]{#2}%
+ \fi\fi\fi\fi\fi%
+ \else\if\@tmpa q%1,4-quinone
+ \if\@tmpb a% (A)%
+ \hanthracenev[bfhjlo]{#2}%
+ \else\ifx\@tmpb\empty% (A)
+ \hanthracenev[behjmp]{#2}%
+ \else\if\@tmpb A% circle type
+ \hanthracenev[bBC]{#2}%
+ \else%
+ \hanthracenev[behjmp]{#2}%
+ \fi\fi\fi%
+ \else
+ \hanthracenev[@#1]{#2}%
+ \fi\fi\fi\fi\fi\fi%
+}% %end of \anthracenev macro%
+\def\hphenanthrenev{%
+ \@ifnextchar[{\@hphenanthrenev[@}{\@hphenanthrenev[r]}}
+\def\@hphenanthrenev[#1]#2{%
+\@reset@ylsw\reset@@yl
+\ylposition{#2}{-4}{0}{2}{0}% %for 5 position
+\if@ylsw \ifx\@@ylii\empty
+\def\@@ylii{0}\def\@@yli{0}\fi
+\else
+\ylposition{#2}{12}{3}{7}{-1}% %for 6 to 8 positions
+\fi
+\if@ylsw\ifx\@@ylii\empty
+\def\@@ylii{0}\def\@@yli{0}\fi\else
+\ylposition{#2}{13}{2}{5}{-1}% %for 9 to 10 positions
+\fi
+\if@ylsw\ifx\@@ylii\empty
+\def\@@ylii{-342}\def\@@yli{0}\fi\else
+\ylposition{#2}{4}{0}{4}{-1}% %for 1 to 3 positions
+\fi
+\if@ylsw\ifx\@@ylii\empty
+\def\@@ylii{-513}\def\@@yli{-303}\fi\else
+\ylposition{#2}{2}{5}{7}{0}% %for 4-position
+\fi
+\if@ylsw\ifx\@@ylii\empty
+\def\@@ylii{-513}\def\@@yli{-303}\fi\else
+\ylfusedposition{#2}{-12}{-1}{1}{0}% % for 4b and 8a
+\fi
+\if@ylsw\ifx\@@ylii\empty
+\def\@@ylii{0}\def\@@yli{0}\fi\else
+\ylfusedposition{#2}{-10}{0}{2}{0}% % for 4a and 10a
+\fi
+\if@ylsw\ifx\@@ylii\empty
+\def\@@ylii{-342}\def\@@yli{0}\fi\fi
+\if@ylsw
+ \yl@shiftii=\@ylii
+ \ifx\@@ylii\empty\else
+ \advance\yl@shiftii\@@ylii\fi
+ \yl@shifti=\@yli
+ \ifx\@@yli\empty\else
+ \advance\yl@shifti\@@yli\fi
+ \advance\yl@shiftii\yl@xdiff
+ \advance\yl@shifti\yl@ydiff
+ \begin{sfpicture}(0,0)(-\yl@shiftii,-\yl@shifti)
+ \reset@yl@xydiff%1999/1/6 by S. Fujita
+\else
+ \begin{sfpicture}(1200,1200)(-\shiftii,-\shifti)
+ \origptoutput{hphenanthrenev}%
+\fi
+ \Put@Line(0,406)(-5,-3){171}% %bond 6-5
+ \Put@Line(0,406)(5,-3){171}% %bond 5-4a
+ \Put@Line(0,0)(-5,3){171}% %bond 8-7
+ \Put@Line(0,0)(5,3){171}% %bond 8-8a
+ \Put@Line(171,103)(0,1){200}% %bond 8a-4b
+ \Put@Line(-171,103)(0,1){200}% %bond 7-6
+ \Put@Line(342,406)(-5,-3){171}% %bond 4a-4b
+ \Put@Line(342,406)(5,-3){171}% %bond 4a-10a
+ \Put@Line(342,0)(-5,3){171}% %bond 9-8a
+ \Put@Line(342,0)(5,3){171}% %bond 9-10
+ \Put@Line(513,103)(0,1){200}% %bond 10-10a
+ %%%%
+ \Put@Line(342,406)(0,1){200}% %bond 4a-4
+ \Put@Line(513,709)(-5,-3){171}% %bond 3-4
+ \Put@Line(513,709)(5,-3){171}% %bond 3-2
+ \Put@Line(684,406)(0,1){200}% %bond 1-2
+ \Put@Line(513,303)(5,3){171}% %bond 10a-1
+\@tfor\member:=#1\do{%
+\if\member r%no endcyclic double bonds
+\else\if\member a%
+ \Put@Line(651,432)(0,1){148}% %double bond 1-2
+\else\if\member b%
+ \Put@Line(519,667)(5,-3){126}% %double bond 3-2
+\else\if\member c%
+ \Put@Line(519,667)(-5,-3){126}% %double bond 3-4
+\else\if\member d%
+ \Put@Line(375,432)(0,1){148}% %double bond 4a-4
+\else\if\member e%
+ \Put@Line(348,364)(-5,-3){126}% %double bond 4a-4b
+\else\if\member f%
+ \Put@Line(6,364)(5,-3){126}% %double bond 5-4b
+\else\if\member g%
+ \Put@Line(-6,364)(-5,-3){126}% %double bond 5-6
+\else\if\member h%
+ \Put@Line(-138,129)(0,1){148}% %double bond 6-7
+\else\if\member i%
+ \Put@Line(-6,42)(-5,3){126}% %double bond 8-7
+\else\if\member j%
+ \Put@Line(6,42)(5,3){126}% %double bond 8-8a
+\else\if\member k%
+ \Put@Line(348,42)(-5,3){126}% %double bond 9-8a
+\else\if\member l%
+ \Put@Line(348,42)(5,3){126}% %double bond 9-10
+\else\if\member m%
+ \Put@Line(482,129)(0,1){148}% %double bond 10-10a
+\else\if\member n%
+ \Put@Line(519,345)(5,3){126}% %double bond 10a-1
+\else\if\member o%
+ \Put@Line(507,345)(-5,3){126}% %double bond 10a-4a
+\else\if\member O%
+ \Put@Line(348,364)(5,-3){126}% %double bond 4a-10a
+\else\if\member p%
+ \Put@Line(138,129)(0,1){148}% %double bond 8a-4b
+\else\if\member P%
+ \Put@Line(204,129)(0,1){148}% %double bond 8a-4b
+\else\if\member C%left aromatic circle
+ \Put@oCircle(0,203){240}% %circle
+\else\if\member B%right aromatic circle
+ \Put@oCircle(342,203){240}% %circle
+\else\if\member A%right aromatic circle
+ \Put@oCircle(513,506){240}% %circle
+\else
+ \expandafter\twoCH@R\member//%
+ \set@fusion@hphenanv
+\fi\fi\fi\fi\fi\fi\fi\fi\fi\fi\fi\fi\fi\fi\fi\fi\fi\fi\fi\fi\fi\fi}%
+\global\drawsamesubsttrue%2002/05/30 warning on
+\Put@Direct(0,0){\setsixringv{#2}{-4}{0}{2}{0}}% %for 5 position
+\global\drawsamesubstfalse%2002/05/30 warning off
+\Put@Direct(0,0){\setsixringv{#2}{12}{3}{7}{-1}}% %for 6 to 8 positions
+\Put@Direct(342,0){\setsixringv{#2}{13}{2}{5}{-1}}% %for 9 to 10 positions
+\Put@Direct(513,303){\setsixringv{#2}{4}{0}{4}{-1}}% %for 1 to 3 positions
+\Put@Direct(513,303){\setsixringv{#2}{2}{5}{7}{0}}% %for 4-position
+\Put@Direct(0,0){\setfusedbond{#2}{-12}{-1}{1}{0}}% % for 4b and 8a
+\Put@Direct(342,0){\setfusedbond{#2}{-10}{0}{2}{0}}% % for 4a and 10a
+\end{sfpicture}}% %end of \hphenanthrenev macro%
+\def\phenanthrenev{\@ifnextchar[{\@phenanthrenev}{\@phenanthrenev[r]}}
+\def\@phenanthrenev[#1]#2{%
+ \iforigpt \typeout{command `phenanthrenev' is %
+ based on `hphenantherenv'.}\fi%
+ \expandafter\threech@r#1{}{}%
+ \if\@tmpa r% right-handed set of double bonds
+ \hphenanthrenev[acgilop]{#2}%
+ \else\if\@tmpa A%aromatic circle
+ \hphenanthrenev[ABC]{#2}%
+ \else\if\@tmpa p%1,4-quinone
+ \if\@tmpb a% (A)%
+ \hphenanthrenev[bgilop]{#2}%
+ \else\ifx\@tmpb\empty% (A)
+ \hphenanthrenev[bgilop]{#2}%
+ \else\if\@tmpb A% circle type
+ \hphenanthrenev[BCb]{#2}%
+ \else
+ \hphenanthrenev[bgilop]{#2}%
+ \fi\fi\fi%
+ \else\if\@tmpa o%o-quinone
+ \if\@tmpb a% (A)%
+ \hphenanthrenev[cgilop]{#2}%
+ \else\ifx\@tmpb\empty% (A)
+ \hphenanthrenev[cgilop]{#2}%
+ \else\if\@tmpb b% (B)
+ \hphenanthrenev[dgilnp]{#2}%
+ \else\if\@tmpb c% (C)
+ \hphenanthrenev[agilop]{#2}%
+ \else\if\@tmpb A% cicle type
+ \hphenanthrenev[cBC]{#2}%
+ \fi\fi\fi\fi\fi%
+ \else\if\@tmpa q%9,10-quinone
+ \if\@tmpb a% (A)%
+ \hphenanthrenev[acgiop]{#2}%
+ \else\ifx\@tmpb\empty% (A)
+ \hphenanthrenev[acgiop]{#2}%
+ \else\if\@tmpb A% circle type
+ \hphenanthrenev[AC]{#2}%
+ \else
+ \hphenanthrenev[acgiop]{#2}%
+ \fi\fi\fi%
+ \else
+ \hphenanthrenev[@#1]{#2}%
+ \fi\fi\fi\fi\fi%
+}% %end of \phenanthrenev macro%
+\def\steroid{\@ifnextchar[{\@steroid[@}{\@steroid[Z]}}
+\def\@steroid[#1]#2{%
+\iniatom\iniflag%initialize
+\@reset@ylsw\reset@@yl
+\yl@steroidposition{#2}%
+\if@ylsw
+ \yl@shiftii=\@ylii
+ \ifx\@@ylii\empty\else
+ \advance\yl@shiftii\@@ylii\fi
+ \yl@shifti=\@yli
+ \ifx\@@yli\empty\else
+ \advance\yl@shifti\@@yli\fi
+ \advance\yl@shiftii\yl@xdiff
+ \advance\yl@shifti\yl@ydiff
+ \begin{sfpicture}(0,0)(-\yl@shiftii,-\yl@shifti)
+ \reset@yl@xydiff%1999/1/6 by S. Fujita
+\else
+ \begin{sfpicture}(1600,1300)(-\shiftii,-\shifti)
+ \origptoutput{steroid}%
+\fi
+ \Put@Direct(0,0){\@steroidskeleton{#1}{#2}}%
+\end{sfpicture}}% %end of \steroid macro%
+\def\yl@steroidposition#1{%
+\ylposition{#1}{0}{0}{2}{0}% %for 1
+\if@ylsw \ifx\@@ylii\empty
+\def\@@ylii{0}\def\@@yli{0}\fi
+\else
+\ylposition{#1}{8}{3}{7}{-1}% %for 2 to 4 positions
+\fi
+\if@ylsw\ifx\@@ylii\empty
+\def\@@ylii{0}\def\@@yli{0}\fi\else
+\ylposition{#1}{10}{2}{5}{-1}% %for 6 to 7 positions
+\fi
+\if@ylsw\ifx\@@ylii\empty
+\def\@@ylii{-342}\def\@@yli{0}\fi\else
+\ylposition{#1}{-11}{0}{2}{0}%for 12 position
+\fi
+\if@ylsw\ifx\@@ylii\empty
+\def\@@ylii{-513}\def\@@yli{-303}\fi\else
+\ylposition{#1}{-5}{5}{7}{0}% %for 11 position
+\fi
+\if@ylsw\ifx\@@ylii\empty
+\def\@@ylii{-513}\def\@@yli{-303}\fi\else
+\ylposition{#1}{18}{0}{4}{-1}%for 15 to 17 positions
+\fi
+\if@ylsw\ifx\@@ylii\empty
+\def\@@ylii{-855}\def\@@yli{-303}\fi\else
+\ylatombondposition{#1}{-4}{7}% % for 5
+\fi
+\if@ylsw\ifx\@@ylii\empty
+\def\@@ylii{-171}\def\@@yli{-103}\fi\else
+\ylatombondposition{#1}{-9}{1}% % for 10
+\fi
+\if@ylsw\ifx\@@ylii\empty
+\def\@@ylii{-171}\def\@@yli{-303}\fi\else
+\ylatombondposition{#1}{-7}{1}% % for 8
+\fi
+\if@ylsw\ifx\@@ylii\empty
+\def\@@ylii{-513}\def\@@yli{-303}\fi\else
+\ylatombondposition{#1}{-8}{7}% % for 9
+\fi
+\if@ylsw\ifx\@@ylii\empty
+\def\@@ylii{-342}\def\@@yli{-406}\fi\else
+\ylatombondposition{#1}{-13}{7}% % for 14
+\fi
+\if@ylsw\ifx\@@ylii\empty
+\def\@@ylii{-684}\def\@@yli{-406}\fi\else
+\ylatombondposition{#1}{-12}{1}% % for 13
+\fi
+\if@ylsw\ifx\@@ylii\empty
+\def\@@ylii{-684}\def\@@yli{-606}\fi\fi%
+}% end of \yl@steroidposition
+\def\@steroidskeleton#1#2{%
+ \Put@Line(0,406)(-5,-3){171}% %bond 1-2
+ \Put@Line(0,406)(5,-3){171}% %bond 1-10
+ \Put@Line(0,0)(-5,3){171}% %bond 4-3
+ \Put@Line(0,0)(5,3){171}% %bond 4-5
+ \Put@Line(171,103)(0,1){200}% %bond 5-10
+ \Put@Line(-171,103)(0,1){200}% %bond 3-2
+ \Put@Line(342,406)(-5,-3){171}% %bond 9-10
+ \Put@Line(342,406)(5,-3){171}% %bond 9-8
+ \Put@Line(342,0)(-5,3){171}% %bond 6-5
+ \Put@Line(342,0)(5,3){171}% %bond 6-7
+ \Put@Line(513,103)(0,1){200}% %bond 7-8
+ %%%%
+ \Put@Line(342,406)(0,1){200}% %bond 9-11
+ \Put@Line(513,709)(-5,-3){171}% %bond 12-11
+ \Put@Line(513,709)(5,-3){171}% %bond 12-13
+ \Put@Line(684,406)(0,1){200}% %bond 14-13
+ \Put@Line(513,303)(5,3){171}% %bond 8-14
+ %%%%
+ \Put@Line(855,709)(-5,-3){171}% %bond 17-13
+ \Put@Line(855,709)(5,-3){171}% %bond 17-16
+ \Put@Line(1026,406)(0,1){200}% %bond 15-16
+ \Put@Line(684,406)(1,0){342}% %bond 14-15
+\@tfor\member:=#1\do{%
+\if\member Z%no endcyclic double bonds
+\else\if\member a%
+ \Put@Line(-6,364)(-5,-3){126}% %double bond 1-2 5-6
+\else\if\member b%
+ \Put@Line(-138,129)(0,1){148}% %double bond 3-2 6-7
+\else\if\member c%
+ \Put@Line(-6,42)(-5,3){126}% %double bond 4-3 8-7
+\else\if\member d%
+ \Put@Line(6,42)(5,3){126}% %double bond 4-5 8-8a
+\else\if\member e%
+ \Put@Line(348,42)(-5,3){126}% %double bond 6-5 9-8a
+\else\if\member f%
+ \Put@Line(348,42)(5,3){126}% %double bond 6-7 9-10
+\else\if\member g%
+ \Put@Line(482,129)(0,1){148}% %double bond 7-8 10-10a
+\else\if\member h%
+ \Put@Line(507,345)(-5,3){126}% %double bond 8-9 10a-4a
+\else\if\member H%
+ \Put@Line(348,364)(5,-3){126}% %double bond 9-8 4a-10a
+\else\if\member i%
+ \Put@Line(348,364)(-5,-3){126}% %double bond 9-10 4a-4b
+\else\if\member j%
+ \Put@Line(6,364)(5,-3){126}% %double bond 1-10 5-4b
+\else\if\member k%
+ \Put@Line(138,129)(0,1){148}% %double bond 5-10 8a-4b
+\else\if\member K%
+ \Put@Line(204,129)(0,1){148}% %double bond 5-10 8a-4b
+\else\if\member l%
+ \Put@Line(375,432)(0,1){148}% %double bond 9-11 4-5
+\else\if\member m%
+ \Put@Line(519,667)(-5,-3){126}% %double bond 12-11 3-4
+\else\if\member n%
+ \Put@Line(519,667)(5,-3){126}% %double bond 12-13 3-2
+\else\if\member o%
+ \Put@Line(651,432)(0,1){148}% %double bond 13-14 1-2
+\else\if\member O%
+ \Put@Line(717,432)(0,1){148}% %double bond 13-14 1-2
+\else\if\member p%
+ \Put@Line(519,345)(5,3){126}% %double bond 8-14 10a-1
+\else\if\member q%
+ \Put@Line(720,439)(1,0){260}% %double bond 14-15
+\else\if\member r%
+ \Put@Line(993,432)(0,1){148}% %double bond 15-16 1-2
+\else\if\member s%
+ \Put@Line(861,667)(5,-3){126}% %double bond 17-16 3-2
+\else\if\member t%
+ \Put@Line(861,667)(-5,-3){126}% %double bond 17-13 3-4
+\else\if\member A%left aromatic circle
+ \Put@oCircle(0,203){240}% %circle
+\else\if\member B%right aromatic circle
+ \Put@oCircle(342,203){240}% %circle
+\else\if\member C%right aromatic circle
+ \Put@oCircle(513,506){240}% %circle
+\else
+ \expandafter\twoCH@R\member//%
+ \set@fusion@steroid
+\fi\fi\fi\fi\fi\fi\fi\fi\fi\fi\fi\fi\fi\fi\fi\fi\fi\fi%
+\fi\fi\fi\fi\fi\fi\fi\fi\fi}%
+\iniflag
+\global\drawsamesubsttrue%2002/05/30 warning on
+\Put@Direct(0,0){\setsixringv{#2}{0}{0}{2}{0}}% %for 1
+\global\drawsamesubstfalse%2002/05/30 warning off
+\Put@Direct(0,0){\setsixringv{#2}{8}{3}{7}{-1}}% %for 2 to 4 positions
+\Put@Direct(342,0){\setsixringv{#2}{10}{2}{5}{-1}}% %for 6 to 7 positions
+\Put@Direct(513,303){\setsixringv{#2}{-11}{0}{2}{0}}%for 12 position
+\Put@Direct(513,303){\setsixringv{#2}{-5}{5}{7}{0}}% %for 11 position
+\Put@Direct(855,303){\setsixringv{#2}{18}{0}{4}{-1}}%for 15 to 17 positions
+\Put@Direct(171,103){\setatombond{#2}{-4}{7}}% % for 5
+\Put@Direct(171,303){\setatombond{#2}{-9}{1}}% % for 10
+\Put@Direct(513,303){\setatombond{#2}{-7}{1}}% % for 8
+\Put@Direct(342,406){\setatombond{#2}{-8}{7}}% % for 9
+\Put@Direct(684,406){\setatombond{#2}{-13}{7}}% % for 14
+\Put@Direct(684,606){\setatombond{#2}{-12}{1}}% % for 13
+}% end of \@steroidskeleton
+\def\set@fusion@steroid{%
+ \let\@@tmpa=\@tmpa
+ \let\@@tmpb=\@tmpb
+ \if\@tmpa a%
+ \edef\@@tmpa{f}%
+ \Put@Direct(0,0){\set@fusionadd@sixv}%
+ \else\if\@tmpa A%
+ \edef\@@tmpa{F}%
+ \Put@Direct(0,0){\set@fusionadd@sixv}%
+ \else\if\@tmpa b%
+ \edef\@@tmpa{e}%
+ \Put@Direct(0,0){\set@fusionadd@sixv}%
+ \else\if\@tmpa B%
+ \edef\@@tmpa{E}%
+ \Put@Direct(0,0){\set@fusionadd@sixv}%
+ \else\if\@tmpa c%
+ \edef\@@tmpa{d}%
+ \Put@Direct(0,0){\set@fusionadd@sixv}%
+ \else\if\@tmpa C%
+ \edef\@@tmpa{D}%
+ \Put@Direct(0,0){\set@fusionadd@sixv}%
+ \else\if\@tmpa d%
+ \edef\@@tmpa{c}%
+ \Put@Direct(0,0){\set@fusionadd@sixv}%
+ \if@smallringsw\else
+ \XyMTeXWarning{Unfavorable Fusion for bond `d'}%
+ \fi
+ \else\if\@tmpa D%
+ \edef\@@tmpa{C}%
+ \Put@Direct(0,0){\set@fusionadd@sixv}%
+ \if@smallringsw\else
+ \XyMTeXWarning{Unfavorable Fusion for bond `D'}%
+ \fi
+ \else\if\@tmpa e%
+ \edef\@@tmpa{d}%
+ \Put@Direct(342,0){\set@fusionadd@sixv}%
+ \if@smallringsw\else
+ \XyMTeXWarning{Unfavorable Fusion for bond `e'}%
+ \fi
+ \else\if\@tmpa E%
+ \edef\@@tmpa{D}%
+ \Put@Direct(342,0){\set@fusionadd@sixv}%
+ \if@smallringsw\else
+ \XyMTeXWarning{Unfavorable Fusion for bond `E'}%
+ \fi
+ \else\if\@tmpa f%
+ \edef\@@tmpa{c}%
+ \Put@Direct(342,0){\set@fusionadd@sixv}%
+ \if@smallringsw\else
+ \XyMTeXWarning{Unfavorable Fusion for bond `f'}%
+ \fi
+ \else\if\@tmpa F%
+ \edef\@@tmpa{C}%
+ \Put@Direct(342,0){\set@fusionadd@sixv}%
+ \if@smallringsw\else
+ \XyMTeXWarning{Unfavorable Fusion for bond `f'}%
+ \fi
+ \else\if\@tmpa g%
+ \edef\@@tmpa{b}%
+ \Put@Direct(342,0){\set@fusionadd@sixv}%
+ \if@smallringsw\else
+ \XyMTeXWarning{Unfavorable Fusion for bond `g'}%
+ \fi
+ \else\if\@tmpa G%
+ \edef\@@tmpa{B}%
+ \Put@Direct(342,0){\set@fusionadd@sixv}%
+ \if@smallringsw\else
+ \XyMTeXWarning{Unfavorable Fusion for bond `g'}%
+ \fi
+ \else\if\@tmpa h%
+ \edef\@@tmpa{a}%
+ \Put@Direct(342,0){\set@fusionadd@sixv}%
+ \if@smallringsw\else
+ \XyMTeXWarning{Forbidden Fusion for bond `h'}%
+ \fi
+ \else\if\@tmpa H%
+ \edef\@@tmpa{A}%
+ \Put@Direct(342,0){\set@fusionadd@sixv}%
+ \if@smallringsw\else
+ \XyMTeXWarning{Forbidden Fusion for bond `H'}%
+ \fi
+ \else\if\@tmpa i%
+ \edef\@@tmpa{f}%
+ \Put@Direct(342,0){\set@fusionadd@sixv}%
+ \if@smallringsw\else
+ \XyMTeXWarning{Unfavorable Fusion for bond `i'}%
+ \fi
+ \else\if\@tmpa I%
+ \edef\@@tmpa{F}%
+ \Put@Direct(342,0){\set@fusionadd@sixv}%
+ \if@smallringsw\else
+ \XyMTeXWarning{Unfavorable Fusion for bond `I'}%
+ \fi
+ \else\if\@tmpa j%
+ \edef\@@tmpa{a}%
+ \Put@Direct(0,0){\set@fusionadd@sixv}%
+ \if@smallringsw\else
+ \XyMTeXWarning{Unfavorable Fusion for bond `j'}%
+ \fi
+ \else\if\@tmpa J%
+ \edef\@@tmpa{A}%
+ \Put@Direct(0,0){\set@fusionadd@sixv}%
+ \if@smallringsw\else
+ \XyMTeXWarning{Unfavorable Fusion for bond `J'}%
+ \fi
+ \else\if\@tmpa k%
+ \edef\@@tmpa{b}%
+ \Put@Direct(0,0){\set@fusionadd@sixv}%
+ \if@smallringsw\else
+ \XyMTeXWarning{Forbidden Fusion for bond `k'}%
+ \fi
+ \else\if\@tmpa K%
+ \edef\@@tmpa{B}%
+ \Put@Direct(0,0){\set@fusionadd@sixv}%
+ \if@smallringsw\else
+ \XyMTeXWarning{Forbidden Fusion for bond `K'}%
+ \fi
+ \else\if\@tmpa l%
+ \edef\@@tmpa{e}%
+ \Put@Direct(513,303){\set@fusionadd@sixv}%
+ \if@smallringsw\else
+ \XyMTeXWarning{Unfavorable Fusion for bond `l'}%
+ \fi
+ \else\if\@tmpa L%
+ \edef\@@tmpa{E}%
+ \Put@Direct(513,303){\set@fusionadd@sixv}%
+ \if@smallringsw\else
+ \XyMTeXWarning{Unfavorable Fusion for bond `L'}%
+ \fi
+ \else\if\@tmpa m%
+ \edef\@@tmpa{f}%
+ \Put@Direct(513,303){\set@fusionadd@sixv}%
+ \else\if\@tmpa M%
+ \edef\@@tmpa{F}%
+ \Put@Direct(513,303){\set@fusionadd@sixv}%
+ \else\if\@tmpa n%
+ \edef\@@tmpa{a}%
+ \Put@Direct(513,303){\set@fusionadd@sixv}%
+ \if@smallringsw\else
+ \XyMTeXWarning{Unfavorable Fusion for bond `n'}%
+ \fi
+ \else\if\@tmpa N%
+ \edef\@@tmpa{A}%
+ \Put@Direct(513,303){\set@fusionadd@sixv}%
+ \if@smallringsw\else
+ \XyMTeXWarning{Unfavorable Fusion for bond `N'}%
+ \fi
+ \else\if\@tmpa o%
+ \edef\@@tmpa{b}%
+ \Put@Direct(513,303){\set@fusionadd@sixv}%
+ \if@smallringsw\else
+ \XyMTeXWarning{Forbidden Fusion for bond `o'}%
+ \fi
+ \else\if\@tmpa O%
+ \edef\@@tmpa{B}%
+ \Put@Direct(513,303){\set@fusionadd@sixv}%
+ \if@smallringsw\else
+ \XyMTeXWarning{Forbidden Fusion for bond `O'}%
+ \fi
+ \else\if\@tmpa p%
+ \edef\@@tmpa{c}%
+ \Put@Direct(513,303){\set@fusionadd@sixv}%
+ \if@smallringsw\else
+ \XyMTeXWarning{Unfavorable Fusion for bond `N'}%
+ \fi
+ \else\if\@tmpa P%
+ \edef\@@tmpa{C}%
+ \Put@Direct(513,303){\set@fusionadd@sixv}%
+ \if@smallringsw\else
+ \XyMTeXWarning{Unfavorable Fusion for bond `N'}%
+ \fi
+ \else\if\@tmpa q%
+ \XyMTeXWarning{Mismatched dimension for bond `q'}%
+ \else\if\@tmpa Q%
+ \XyMTeXWarning{Mismatched dimension for bond `Q'}%
+ \else\if\@tmpa r%
+ \edef\@@tmpa{b}%
+ \Put@Direct(855,303){\set@fusionadd@sixv}%
+ \else\if\@tmpa R%
+ \edef\@@tmpa{B}%
+ \Put@Direct(855,303){\set@fusionadd@sixv}%
+ \else\if\@tmpa s%
+ \edef\@@tmpa{a}%
+ \Put@Direct(855,303){\set@fusionadd@sixv}%
+ \else\if\@tmpa S%
+ \edef\@@tmpa{A}%
+ \Put@Direct(855,303){\set@fusionadd@sixv}%
+ \else\if\@tmpa t%
+ \edef\@@tmpa{f}%
+ \Put@Direct(855,303){\set@fusionadd@sixv}%
+ \if@smallringsw\else
+ \XyMTeXWarning{Unfavorable Fusion for bond `t'}%
+ \fi
+ \else\if\@tmpa T%
+ \edef\@@tmpa{F}%
+ \Put@Direct(855,303){\set@fusionadd@sixv}%
+ \if@smallringsw\else
+ \XyMTeXWarning{Unfavorable Fusion for bond `T'}%
+ \fi
+ \fi\fi\fi\fi\fi\fi\fi\fi%
+ \fi\fi\fi\fi\fi\fi\fi\fi\fi\fi%
+ \fi\fi\fi\fi\fi\fi\fi\fi\fi\fi\fi\fi%
+ \fi\fi\fi\fi\fi\fi\fi\fi\fi\fi%
+}% end of the macro \set@fusion@steroid
+\def\steroidchain{\@ifnextchar[{\@steroidchain[@}{\@steroidchain[Z]}}
+\def\@steroidchain[#1]#2{%
+\@reset@ylsw\reset@@yl
+\yl@steroidposition{#2}%
+\ylposition{#2}{-21}{0}{3}{0}%for 22 and 23 positions
+\if@ylsw \ifx\@@ylii\empty
+\def\@@ylii{-1026}\def\@@yli{-606}\fi
+\else
+\ylposition{#2}{-14}{5}{7}{0}%for 20 position
+\fi
+\if@ylsw\ifx\@@ylii\empty
+\def\@@ylii{-1026}\def\@@yli{-606}\fi\else
+\ylposition{#2}{-20}{3}{5}{0}%for 24 position
+\fi
+\if@ylsw\ifx\@@ylii\empty
+\def\@@ylii{-1197}\def\@@yli{-709}\fi\else
+\ylatombondposition{#2}{-24}{4}% % for 5
+\fi
+\if@ylsw\ifx\@@ylii\empty
+\def\@@ylii{-1397}\def\@@yli{-709}\fi\fi
+\if@ylsw
+ \yl@shiftii=\@ylii
+ \ifx\@@ylii\empty\else
+ \advance\yl@shiftii\@@ylii\fi
+ \yl@shifti=\@yli
+ \ifx\@@yli\empty\else
+ \advance\yl@shifti\@@yli\fi
+ \advance\yl@shiftii\yl@xdiff
+ \advance\yl@shifti\yl@ydiff
+ \begin{sfpicture}(0,0)(-\yl@shiftii,-\yl@shifti)%
+ \reset@yl@xydiff%1999/1/6 by S. Fujita
+\else
+ \begin{sfpicture}(2000,1500)(-\shiftii,-\shifti)%
+ \iforigpt \typeout{command `steroidchain' is based on `steroid'.}\fi%
+\fi
+ \Put@Direct(0,0){\@steroidskeleton{#1}{#2}}%
+ \Put@Line(855,709)(0,1){200}% %bond 17-20
+ \Put@Line(1026,1012)(-5,-3){171}% %bond 22-20
+ \Put@Line(1026,1012)(5,-3){171}% %bond 22-23
+ \Put@Line(1197,709)(0,1){200}% %bond 24-23
+ \Put@Line(1197,709)(1,0){200}% %bond 24-25
+ \Put@Line(1397,709)(3,5){103}% %bond 25-26
+ \Put@Line(1397,709)(3,-5){103}% %bond 25-27
+\@tfor\member:=#1\do{%
+\expandafter\twoCH@R\member//\relax%
+\if\@tmpa Z\relax%
+ \ifx\@tmpb\empty%no action
+ \else\if\@tmpb a%
+ \Put@Line(888,735)(0,1){148}% %double bond 17-20
+ \else\if\@tmpb b%
+ \Put@Line(1020,970)(-5,-3){126}% %double bond 22-20
+ \else\if\@tmpb c%
+ \Put@Line(1032,970)(5,-3){126}% %double bond 22-23
+ \else\if\@tmpb d%
+ \Put@Line(1164,735)(0,1){148}% %double bond 24-23
+ \else\if\@tmpb e%
+ \Put@Line(1233,742)(1,0){140}% %double bond 24-25
+ \else\if\@tmpb f%
+ \Put@Line(1433,715)(3,5){72}% %double bond 25-26
+ \else\if\@tmpb g%
+ \Put@Line(1433,697)(3,-5){72}% %double bond 25-27
+ \fi\fi\fi\fi\fi\fi\fi\fi\fi}%
+\Put@Direct(1026,606){\setsixringv{#2}{-21}{0}{3}{0}}%for 22 and 23 positions
+\Put@Direct(1026,606){\setsixringv{#2}{-14}{5}{7}{0}}%for 20 position
+\Put@Direct(1197,709){\setsixringv{#2}{-20}{3}{5}{0}}%for 24 position
+\Put@Direct(1397,709){\setatombond{#2}{-24}{4}}% % for 5
+\end{sfpicture}}% %end of \steroidchain macro%
+\endinput
+%%
+%% End of file `carom.sty'.