Yet With another problem. In the data I'm using I have a lot of sub and super scripts (see example below). I put (or acctually Word2latex) between $'s to mark it as an equation, other wise I get allot of errors. But I don't want the sub or super script to be italic. Is there away a can prevent this for the whole document? And is there than away I can undo that for a few equations??
Thanx again for the help.
And ohey some expamples:
the Latex file: (it's part of a bigger project so this will not produce a pdf)
Code: Select all
% Chapter 1
\chapter{\bfseries{\textsf{General Introduction and Outline}}} % Write in your own chapter title
\label{Chapter1}
\lhead{\emph{Introduction}} % Write in your own chapter title to set the page header
\renewcommand{\bibname}{References}
\section{Biological Introduction}
\section{}
Kijken of we ook een ref kunnen gebruiken \cite{abdel1996}
\ce{H2SO4} [\alpha]^{22}_{\textsc{d}}
\subsection{A (not so short) Introduction to}
test\cite{abdel1996}\\
\textbf{1,6-Anhydro-2-azido-3-\textit{O}-benzyl-2-deoxy-4-\textit{O}-methyl-\beta-\textsc{d}-glu\-co\-pyr\-anose (X):}\\
Compound X (xmmol, x g) was dissolved in DMF and cooled using an ice-bath
and after stirring for 15 minutes NaH (1.5 equiv. x mmol, x g) was added
portion wise. After 30 minutes the gas development stopped and MeI (1.2
equiv. x mmol, x mL) was added drop wise. The reaction was quenched with
MeOH after 1.5 hours. The reaction mixture was concentrated and purified
using a short silica column (20{\%} EtOAc/PE) which gave product X as clear
oil.\textbf{$^{1}$H NMR (400 MHz, CDCl$_{3}$)} $\delta$ 7.41 - 7.27 (m, 5H,
CH$_{arom}$, Bn), 5.48 (s, 1H, H$_{1}$), 4.64 (m, 3H, CH$_{2}$Bn, H$_{5}$),
4.08 (d, \textit{J} = 7.2 Hz, 1H, H$_{6'}$), 3.76 (dd, J = 13.0, 6.4 Hz, 1H,
H$_{6}$), 3.59 (d, \textit{J} = 24.3 Hz, 1H, H$_{4}$), 3.39 (s, 3H, CH$_{3}$), 3.29
(s, 1H, H$_{3}$), 3.20 (s, 1H, H$_{2}$); \textbf{$^{13}$C NMR (101 MHz,
CDCl$_{3}$)} \delta 137.38 (C$_{q}$, Bn), 128.68-127.88 (CH$_{arom}$, Bn),
100.64 (C-1), 78.80 (C-2), 75.92 (C-3), 73.75 (C-4), 72.51 (C-6), 65.34
(CH$_{2}$, Bn), 59.87 (C-5), 57.16 (CH$_{3}$, Me); \textbf{IR:} 2096.5,
1718.5, 1244.0, 1099.3, 1004.8, 929.6, 867.9; \\
\textbf{1,6-Di-\textit{O}-acteyl-2-azido-3-\textit{O}-benzyl-2-deoxy-4-\textit{O}-methyl-$\alpha
-\beta$-\textbf{d}-glucopyranose (X):}
The clear oil (X) was taken up in \ce{Ac2o} and cooled with an ice bath. To
this cooled solution TFA (10{\%} v/v) was added and the reaction was stirred
overnight to room temperature. After complete conversion of the starting
material on TLC the reaction was diluted with Toluene and co-evaporated to
yellow oil. Purification using a short silica column (30{\%} EtOAc/PE)
yielded compound X (2.62 g, 6.66 mmol, 90{\%}) as a white solid.\textbf{$^{
1}$H NMR} (400 MHz, CDCl$_{3}$)$\delta$ 7.43 -- 7.23 (m, 5H,
CH$_{arom}$, Bn $\alpha $/$\beta $ ), 6.22 (d, $J$ = 3.6 Hz, 1H, H$_{1\alpha
})$, 5.45 (d, $J$ = 8.1 Hz, 1H, H$_{1\beta })$ 4.88 -- 4.81 (m, 2H, CH$_{2}$ Bn
$\alpha $/$\beta )$, 4.30 - 4.21 (m, 2H, CH$_{2, }$H$_{6\alpha /\beta })$,
3.87 - 3.78 (m, 2H, H$_{5\alpha /\beta }$ H$_{4\alpha$/$\beta })$, 3.55 -
3.45 (m, 4H, CH$_{3, }$Me, H$_{3\alpha$/$\beta })$, 3.30 (t, $J$ = 9.5 Hz, 1H,
H$_{2\alpha /\beta })$, 2.09 (s, 3H, CH$_{3}$, OAc), 2.04 (s, 3H CH$_{3}$,
OAc);\textbf{$^{13}$C NMR} (101 MHz, CDCl$_{3}$)$\delta $ 170.09 (C$_{q}$,
Ac), 168.31 (C$_{q}$, Ac), 137.40 (C$_{q}$, Bn), 128.16-127.67 (CH$_{arom}$,
Bn), 92.24 (C-1$_{\beta })$, 89.96 (C-1$_{\alpha })$, 82.38 (C-4$_{\beta
})$, 79.90 (C-4$_{\alpha })$, 79.51 (C-3$_{\alpha })$, 79.12 (C-3$_{\beta
})$, 75.10 (CH$_{2}$, Bn), 73.53 (C-5$_{\beta })$, 71.03 (C-5$_{\alpha })$,
64.46 (CH$_{3}$, Me$_{\beta })$, 62.12 (CH$_{2}$, C-6$_{\alpha /\beta })$,
62.06 (CH$_{3}$, Me$_{\alpha })$, 60.56 (C-2$_{\alpha })$, 60.40
(C-2$_{\beta })$, 20.44 (CH$_{3}$, OAc), 20.30 (CH$_{3}$, OAc); \textbf{IR:}
2106.1, 1753.2, 1733.9, 1373.2, 1136.0, 1109.0, 1004.8, 935.4, 906.5, 740.6
\bibliographystyle{achemso}
{\bibliography{chapter1}}
\BoudewijnD
