Fix capitalization in compound names

Author: davidlmobley

paper/benchmarkset.tex

@@ -371,13 +371,13 @@ \subsubsection{Cucurbiturils}
 \midrule
 
 1  & memantine                          & 4054      & \parbox[c]{1em}{\includegraphics[scale=0.2]{figures/4054.pdf}}      & CC12CC3CC(C1)(CC(C3)(C2)N)C                  & -5.99 \pm 0.05  & \kern-1em {$^{\rm d}$}  \\
-3  & 1,3-Bis(trimethylaminio)adamantane	& 101379195 & \parbox[c]{1em}{\includegraphics[scale=0.2]{figures/101379195.pdf}} & C[N+](C)(C)C12CC3CC(C1)CC(C3)(C2)[N+](C)(C)C & -6.55 \pm 0.05  & \kern-1em {$^{\rm d}$}  \\
-5  & N-(1-Adamantyl)ethylenediamine     & 303798    & \parbox[c]{1em}{\includegraphics[scale=0.2]{figures/303798.pdf}}    & C1C2CC3CC1CC(C2)(C3)NCCN                     & -18.22 \pm 0.09 & \kern-1em {$^{\rm e}$}  \\
+3  & 1,3-bis(trimethylaminio)adamantane	& 101379195 & \parbox[c]{1em}{\includegraphics[scale=0.2]{figures/101379195.pdf}} & C[N+](C)(C)C12CC3CC(C1)CC(C3)(C2)[N+](C)(C)C & -6.55 \pm 0.05  & \kern-1em {$^{\rm d}$}  \\
+5  & N-(1-adamantyl)ethylenediamine     & 303798    & \parbox[c]{1em}{\includegraphics[scale=0.2]{figures/303798.pdf}}    & C1C2CC3CC1CC(C2)(C3)NCCN                     & -18.22 \pm 0.09 & \kern-1em {$^{\rm e}$}  \\
 17 & adamantane-1,3-diamine             & 213512    & \parbox[c]{1em}{\includegraphics[scale=0.2]{figures/213512.pdf}}    & C1C2CC3(CC1CC(C2)(C3)N)N                     & -11.33 \pm 0.05 & \kern-1em {$^{\rm d}$}  \\
-18 & 1-Adamantanecarboxylic acid        & 13235     & \parbox[c]{1em}{\includegraphics[scale=0.2]{figures/13235.pdf}}     & C1C2CC3CC1CC(C2)(C3)C(=O)O                   & -11.59 \pm 0.06 & \kern-1em {$^{\rm d}$}  \\
+18 & 1-adamantanecarboxylic acid        & 13235     & \parbox[c]{1em}{\includegraphics[scale=0.2]{figures/13235.pdf}}     & C1C2CC3CC1CC(C2)(C3)C(=O)O                   & -11.59 \pm 0.06 & \kern-1em {$^{\rm d}$}  \\
 22 & 1-Adamantyltrimethylaminium        & 3010127   & \parbox[c]{1em}{\includegraphics[scale=0.2]{figures/3010127.pdf}}   & C[N+](C)(C)C12CC3CC(C1)CC(C3)C2              & -16.66 \pm 0.08 & \kern-1em {$^{\rm d}$}  \\
 23 & amantadine                         & 2130      & \parbox[c]{1em}{\includegraphics[scale=0.2]{figures/2130.pdf}}      & C1C2CC3CC1CC(C2)(C3)N                        & -17.19 \pm 0.08 & \kern-1em {$^{\rm d}$}  \\
-24 & N-(1-Adamantyl)pyridinium          & 3848257   & \parbox[c]{1em}{\includegraphics[scale=0.2]{figures/3848257.pdf}}   & C1C2CC3CC1CC(C2)(C3)[N+]4=CC=CC=C4           & -16.75 \pm 0.07 & \kern-1em {$^{\rm d}$}  \\
+24 & N-(1-adamantyl)pyridinium          & 3848257   & \parbox[c]{1em}{\includegraphics[scale=0.2]{figures/3848257.pdf}}   & C1C2CC3CC1CC(C2)(C3)[N+]4=CC=CC=C4           & -16.75 \pm 0.07 & \kern-1em {$^{\rm d}$}  \\
 
 \bottomrule
 \end{tabular}\\
@@ -399,7 +399,7 @@ \subsubsection{Cucurbiturils}
 2   & dopamine                 & 681       & \parbox[c]{1em}{\includegraphics[scale=0.2]{figures/681.pdf}}   & C1=CC(=C(C=C1CCN)O)O                 & -6.31 \pm 0.05                                            \\
 4   & o-phenylenediamine       & 7243      & \parbox[c]{1em}{\includegraphics[scale=0.2]{figures/7243.pdf}}  & C1=CC=C(C(=C1)N)N                    & -6.68 \pm 0.05                                            \\
 5   & m-phenylenediamine       & 7935      & \parbox[c]{1em}{\includegraphics[scale=0.2]{figures/7935.pdf}}  & C1=CC(=CC(=C1)N)N                    & -6.69 \pm 0.02                                            \\
-7   & 4-(Aminomethyl)pyridine  & 77317     & \parbox[c]{1em}{\includegraphics[scale=0.2]{figures/77317.pdf}} & C1=CN=CC=C1CN                        & -7.56 \pm 0.06                                            \\
+7   & 4-(aminomethyl)pyridine  & 77317     & \parbox[c]{1em}{\includegraphics[scale=0.2]{figures/77317.pdf}} & C1=CN=CC=C1CN                        & -7.56 \pm 0.06                                            \\
 8   & p-phenylenediamine       & 7814      & \parbox[c]{1em}{\includegraphics[scale=0.2]{figures/7814.pdf}}  & C1=CC(=CC=C1N)N                      & -8.60 \pm 0.06                                            \\
 9   & p-toluidine              & 7813      & \parbox[c]{1em}{\includegraphics[scale=0.2]{figures/7813.pdf}}  & CC1=CC=C(C=C1)N                      & -9.43 \pm 0.05                                            \\
 20  & p-xylylenediamine        & 68315     & \parbox[c]{1em}{\includegraphics[scale=0.2]{figures/68315.pdf}} & C1=CC(=CC=C1CN)CN                    & -12.62 \pm 0.06                                           \\