1,3- versus 1,4-Asymmetric induction in Mukaiyama–Michael additions of optically active ketene acetals to 2-methylcyclopent-2-en-1-one: a remarkable inversion of facial selectivity-Reference-Cited by-同舟云学术

1,3- versus 1,4-Asymmetric induction in Mukaiyama–Michael additions of optically active ketene acetals to 2-methylcyclopent-2-en-1-one: a remarkable inversion of facial selectivity

Published:2001-02 Issue:6 Volume:42 Page:1135-1138
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Gorobets Evgueni,Urbanczyk-Lipkowska Zofia,Stepanenko Viatcheslav,Wicha Jerzy

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference23 articles.

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3. Oare, D. A.; Heathcock, C. H. In Topics in Stereochemistry; Eliel, E. L.; Wilen, S. H., Eds.; John Wiley & Sons: New York, 1991; Vol. 20, pp. 87–170.

4. Furans in synthesis. 11. Total syntheses of (.+-.)- and (-)-fastigilin C

5. Acyclic stereoselection. Part 34. Stereoselection in the Michael addition reaction. 4. Diastereofacial preferences in Lewis acid-mediated additions of enolsilanes to chiral enones

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