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π-Facial diastereoselection in reductions of sterically unbiased ketones containing the norbornyl framework: Further tests for theoretical models
G. Mehta
,
Faiz Ahmed Khan
,
B. Ganguly
,
J. Chandrasekhar
Published in
1994
DOI:
10.1039/p29940002275
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.
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Journal Details
Authors (1)
About the journal
Journal
Journal of the Chemical Society, Perkin Transactions 1
ISSN
1472779X
Authors (1)
Faiz Ahmed Khan
Department of Chemistry
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