π-Facial selectivities in nucleophilic additions to 4-hetero-tricyclo[5.2.1.02,6]decan-10-ones and 4-hetero-tricyclo[5.2.1.02,6]dec-8-en-10-ones: an experimental and computational study-Reference-Cited by-同舟云学术

π-Facial selectivities in nucleophilic additions to 4-hetero-tricyclo[5.2.1.02,6]decan-10-ones and 4-hetero-tricyclo[5.2.1.02,6]dec-8-en-10-ones: an experimental and computational study

Published:2002-04 Issue:14 Volume:43 Page:2487-2490
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Mehta Goverdhan,Gagliardini Vanessa,Priyakumar U.Deva,Sastry G.Narahari

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference26 articles.

1. For recent reviews on diastereoselection, see a thematic issue: (a) le Noble, W. J.; Gung, B. E. Chem. Rev. 1999, 99, 1069–1480; (b) Mehta, G.; Chandrasekhar, J. Chem. Rev. 1999, 99, 1437.

2. Electronic control of .pi.-facial selectivities in nucleophilic additions to 7-norbornanones

3. A simple computational model for predicting .pi.-facial selectivity in reductions of sterically unbiased ketones. Relative importance of electrostatic and orbital interactions

4. Importance of orbital and electrostatic interactions in determining π-facial selectivities in nucleophilic additions to endo-substituted bicyclo[2.2.2]octan-2-ones

5. 4-Substituted norsnoutanones: a new probe system for evaluating electronic effects in π-facial selectivity in nucleophilic additions

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