Modulating the stereochemical outcome of the Ireland–Claisen reaction of (E)- and (Z)-allylic glycolates-Reference-Cited by-同舟云学术

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Modulating the stereochemical outcome of the Ireland–Claisen reaction of (E)- and (Z)-allylic glycolates

Published:2012-02 Issue:7 Volume:53 Page:825-828
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Feldman Ken S.,Selfridge Brandon R.

Funder

National Science Foundation

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference9 articles.

1. Claisen rearrangement of allyl esters

2. Highly diastereoselective Lewis acid promoted Claisen–Ireland rearrangement

3. A short, stereocontrolled synthesis of avenaciolide

4. McFarland, C. M.; McIntosh, M. C. In The Claisen Rearrangement: Methods and Applications; Hiersemann, M., Nubbemeyer, U., Eds.; Wiley-VCH Verlag GmbH & Co. KGaA: Weinheim, Germany, 2007; pp 117–120.

5. Claisen Rearrangement over the Past Nine Decades

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3. Stereodivergence in the Ireland–Claisen Rearrangement of α-Alkoxy Esters;Organic Letters;2018-08-02

4. Molecular Rearrangements;Organic Reaction Mechanisms Series;2015-06-02

5. Stereoselective total synthesis of cananginones (D–I) using Ireland–Claisen rearrangement as a key step;Tetrahedron;2014-05

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