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π-Facial diastereoselection in reductions of sterically unbiased ketones containing the norbornyl framework: Further tests for theoretical models
G. Mehta, , B. Ganguly, J. Chandrasekhar
Published in
1994
   
Issue: 11
Pages: 2275 - 2277
Abstract
Ketones 3a-c exhibit syn-face selectivity in borohydride reduction; MNDO and ab initio calculations on model and realistic transition states, respectively, reproduce the preference, but differ on the role of electrostatic and orbital effects.
About the journal
JournalJournal of the Chemical Society, Perkin Transactions 1
ISSN1472779X