Diastereoselective synthesis of 2,3,4-trisubstituted γ-lactols and γ-lactones via regio- and stereocontrolled opening of a 1,2-epoxy-4-hydroxyalkyl carbamate with hetero-nucleophiles-Reference-Cited by-同舟云学术

Diastereoselective synthesis of 2,3,4-trisubstituted γ-lactols and γ-lactones via regio- and stereocontrolled opening of a 1,2-epoxy-4-hydroxyalkyl carbamate with hetero-nucleophiles

Published:1986-01 Issue:31 Volume:27 Page:3595-3598
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Lüßmann Jörg,Hoppe Dieter,Jones Peter G.,Fittschen Christa,Sheldrick George M.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference13 articles.

1. D. Hoppe, J. Lüßmann, P. G. Jones, D. Schmidt, G. M. Sheldrick, Tetrahedron Lett. 26, preceding communication.

2. Die Homoaldol-Reaktion oder wie man Probleme der Regio- und Stereoselektivität in den Griff bekommt

3. The Homoaldol Reaction, or How to Overcome Problems of Regio- and Stereo-selectivity

4. Acid-catalyzed-rearrangement of enol ester epoxides

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