Temperature and Solvent Control of the Stereoselectivity in the Reactions of Singlet Oxygen with Oxazolidinone-Substituted Enecarbamates-Reference-Cited by-同舟云学术

Temperature and Solvent Control of the Stereoselectivity in the Reactions of Singlet Oxygen with Oxazolidinone-Substituted Enecarbamates

Published:2004-08-07 Issue:34 Volume:126 Page:10498-10499
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Poon Thomas¹,Sivaguru J.¹,Franz Roberto¹,Jockusch Steffen¹,Martinez Claudia¹,Washington Ilyas¹,Adam Waldemar¹,Inoue Yoshihisa¹,Turro Nicholas J.¹

Affiliation:

1. Department of Chemistry and Department of Chemical Engineering, Columbia University, 3000 Broadway, Mail Code 3119, New York, New York 10027, Joint Science Department, W.M. Keck Science Center, 925 North Mills Avenue, Claremont McKenna, Pitzer, and Scripps Colleges, Claremont, California 91711, Institut für Organische Chemie, Universität Würzburg, Am Hubland, D-97074 Würzburg (Germany) and Department of Chemistry, University of Puerto Rico, Rio Piedras, Puerto Rico 00931, and ICORP (JST) and Department...

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja048438c

Reference21 articles.

1. 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

2. Wewakazole, a Novel Cyclic Dodecapeptide from a Papua New Guinea Lyngbya majuscula

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