γ-halotiglates, II. A high yield, stereoselective preparation and the conversion to useful trisubstituted olefin synthons-Reference-Cited by-同舟云学术

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γ-halotiglates, II. A high yield, stereoselective preparation and the conversion to useful trisubstituted olefin synthons

Published:1975 Issue:21 Volume:16 Page:1679-1682
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Stotter Philip L.,Hill Kenneth A.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference23 articles.

1. .gamma.-Halotiglates. I. Simple, efficient position-specific annelation of unsymmetrically substituted cyclohexanones

2. P. L. Stotter and K.A. Hill, “Reductive Alkylation-Annelation of Polycyclic Enones”, manuscript in preparation.

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