Enecarbamates as Selective Substrates in Oxidations: Chiral-Auxiliary-Controlled Mode Selectivity and Diastereoselectivity in the [2+2] Cycloaddition and Ene Reaction of Singlet Oxygen and in the Epoxidation by DMD and mCPBA-Reference-Cited by-同舟云学术

Enecarbamates as Selective Substrates in Oxidations: Chiral-Auxiliary-Controlled Mode Selectivity and Diastereoselectivity in the [2+2] Cycloaddition and Ene Reaction of Singlet Oxygen and in the Epoxidation by DMD and mCPBA

Published:2004-02-06 Issue:5 Volume:69 Page:1704-1715
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Adam Waldemar¹,Bosio Sara G.¹,Turro Nicholas J.¹,Wolff Barbara T.¹

Affiliation:

1. Institut für Organische Chemie, Universität Würzburg, Am Hubland, D-97074 Würzburg, Germany, and Department of Chemistry, Columbia University, 3000 Broadway, New York, New York 10027

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo035745c

Reference31 articles.

1. Stereoselective dioxygenation of enoates

2. INVESTIGATIONS ON STEROIDS I. 6-OXOPROGESTERONE AND THE STEREOCHEMICAL CONFIGURATION OF SEVERAL 3,5,6-TRIOLS*

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