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<DIV><FONT face=Arial size=2>Hi,</FONT></DIV>
<DIV><FONT face=Arial size=2>Would this work as well for reducing a nitro group
to amine in the presance of a benzyl or benzyloxy?</FONT></DIV>
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<DIV style="FONT: 10pt arial">----- Original Message ----- </DIV>
<DIV
style="BACKGROUND: #e4e4e4; FONT: 10pt arial; font-color: black"><B>From:</B>
<A title=mugunthan_gee@yahoo.co.in
href="mailto:mugunthan_gee@yahoo.co.in">Mugunthan G</A> </DIV>
<DIV style="FONT: 10pt arial"><B>To:</B> <A title=everybody@orglist.net
href="mailto:everybody@orglist.net">everybody@orglist.net</A> </DIV>
<DIV style="FONT: 10pt arial"><B>Sent:</B> Wednesday, October 04, 2006 7:24
AM</DIV>
<DIV style="FONT: 10pt arial"><B>Subject:</B> ORGLIST: reduction of azide
</DIV>
<DIV><BR></DIV><BR>
<DIV>hi,</DIV>
<DIV> u can very well reduce azide to amine in
presence of other groups like benzyl or benzyloxy, by using
triphenylphosphine in water.</DIV><BR><BR><BR>
<DIV><STRONG><FONT color=#438059>MUGUNTHAN.G <BR>DEPARTMENT OF MEDICINAL
CHEMISTRY <BR>NATIONAL INSTITUTE OF PHARMACEUTICAL EDUCATION AND REASEARCH
<BR>SECTOR-67,PHASE-10, MOHALI <BR>PUNJAB-160062
<BR>INDIA</FONT></STRONG></DIV><!--start copy from here --><A
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