Issue 6, 1994

Diasteoselective conjugate additions reactions of a lithiated allylic sulfoximine to acyclic enones

Abstract

The conjugate addition reactions of lithiated N-p-tosyl S-phenyl-2-enyl sulfoximine 4 with cyclic and acyclic enones gives exclusively 1,4-α adducts, the reactions with acyclic enones are highly diastereoselective.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1994, 751-752

Diasteoselective conjugate additions reactions of a lithiated allylic sulfoximine to acyclic enones

S. G. Pyne, Z. Dong, B. W. Skelton and A. H. White, J. Chem. Soc., Chem. Commun., 1994, 751 DOI: 10.1039/C39940000751

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Spotlight

Advertisements