Highly Diastereoselective Dioxetane Formation in the Photooxygenation of Enecarbamates with an Oxazolidinone Chiral Auxiliary: Steric Control in the [2 + 2] Cycloaddition of Singlet Oxygen through Conformational Alignment-Reference-Cited by-同舟云学术

Highly Diastereoselective Dioxetane Formation in the Photooxygenation of Enecarbamates with an Oxazolidinone Chiral Auxiliary: Steric Control in the [2 + 2] Cycloaddition of Singlet Oxygen through Conformational Alignment

Published:2002-07-01 Issue:30 Volume:124 Page:8814-8815
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Adam Waldemar¹,Bosio Sara G.¹,Turro Nicholas J.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

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja026815k

Reference10 articles.

1. Simplified analogs of the antimalarial artemisinin: synthesis of 6,9-desmethylartemisinin

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