An Asymmetric Route to Novel Chiral Cyclohexenones with Spiro-Connected Cyclopentenes. Further Utility of Chiral Bicyclic Thiolactams and the [3,3] Thio-Claisen Products-Reference-Cited by-同舟云学术

An Asymmetric Route to Novel Chiral Cyclohexenones with Spiro-Connected Cyclopentenes. Further Utility of Chiral Bicyclic Thiolactams and the [3,3] Thio-Claisen Products

Published:1999-04-16 Issue:10 Volume:64 Page:3585-3591
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Lemieux René M.¹,Devine Paul N.¹,Mechelke Mark F.¹,Meyers A. I.¹

Affiliation:

1. Department of Chemistry, Colorado State University, Fort Collins, Colorado 80523

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo982426q

Reference14 articles.

1. Thio-Claisen Rearrangements. An Asymmetric Synthesis of 4,4-Disubstituted Cyclohexenones with Vicinal Quaternary and Tertiary Stereocenters

2. Asymmetric Synthesis of (−)-Trichodiene. Generation of Vicinal Stereogenic Quaternary Centers via the Thio-Claisen Rearrangement

3. Lemieux, R. M.; Meyers, A. I.J. Org. Chem.1998, submitted.

4. Facile regioselective formation of thiopeptide linkages from oligopeptides with new thionation reagents

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