The bicyclo[2.1.1]hexan-2-one system: a new probe for the experimental and computational study of electronic effects in π-facial selectivity in nucleophilic additions
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference22 articles.
1. For recent reviews on diastereoselection, see a thematic issue: Chem. Rev. 1999, 99, 1069–1480; (b) Mehta, G.; Chandrasekhar, J. Chem. Rev. 1999, 99, 1437.
2. Modulation of π-facial selectivities in nucleophilic additions to 7-norbornenones
3. Electronic control of .pi.-facial selectivities in nucleophilic additions to 7-norbornanones
4. A simple computational model for predicting .pi.-facial selectivity in reductions of sterically unbiased ketones. Relative importance of electrostatic and orbital interactions
5. Importance of orbital and electrostatic interactions in determining π-facial selectivities in nucleophilic additions to endo-substituted bicyclo[2.2.2]octan-2-ones
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