From: Robyn L Crumbie (R.Crumbie$##$uws.edu.au)
Date: Sun Apr 09 2000 - 19:42:17 EDT
>You might be able to generate it in situ, eg substrate + ZnCl2 in methanol,
>add NaBH4 with stirring. I know this works for CoCl2/NaBH4 for reducing
>nitriles, nitros and amides, see Tet Lett. no. 52 p4555 1969
>
>Paul Handley
>Dept. of Chemistry
>University of Queensland
>Brisbane, Australia
>__________________
I used this procedure a number of years ago. The only difference was that I
generated the Zn(BH4)2 FIRST, then added the substrate.
Dr Robyn L Crumbie FRACI
Department of Chemistry, UWS Macarthur
PO Box 555
Campbelltown 2560
AUSTRALIA
|\__/,| (`\
_.|o o |_ ) )
~*~---(((----(((---------------------------------------
__________________
ORGLIST - Organic Chemistry Mailing List
Website / Archive / FAQ: http://www.orglist.net/
List coordinator: Joao Aires de Sousa (jas$##$mail.fct.unl.pt)
This archive was generated by hypermail 2.1.4 : Fri Sep 19 2003 - 12:15:34 EDT