Trifluoromethanesulfonic Acid Catalyzed Isomerization of Kinetic Enol Derivatives to the Thermodynamically Favored Isomers-Reference-Cited by-同舟云学术

Trifluoromethanesulfonic Acid Catalyzed Isomerization of Kinetic Enol Derivatives to the Thermodynamically Favored Isomers

Published:2011-06-09 Issue:13 Volume:13 Page:3470-3473
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Lee Phil Ho¹,Kang Dongjin¹,Choi Subin¹,Kim Sunggak¹

Affiliation:

1. Department of Chemistry, Kangwon National University, Chuncheon 200-701, Republic of Korea, and Division of Chemistry and Biological Chemistry, School of Physical and Mathematical Sciences, Nanyang Technological University, Singapore 637371, Singapore

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol2012132

Reference53 articles.

1. The ester enolate Claisen rearrangement. Stereochemical control through stereoselective enolate formation

2. O-Silylated Enolates - Versatile Intermediates for Organic Synthesis

3. Silicon in organic synthesis

4. Silyl Enol Ethers in Synthesis - Part I

5. Silyl Enol Ethers in Synthesis - Part II

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