Origins of Stereoselectivity in the trans Diels−Alder Paradigm-Reference-Cited by-同舟云学术

Origins of Stereoselectivity in the trans Diels−Alder Paradigm

Published:2010-06-17 Issue:27 Volume:132 Page:9335-9340
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Paton Robert S.¹,Mackey Joel L.¹,Kim Woo Han¹,Lee Jun Hee¹,Danishefsky Samuel J.¹,Houk K. N.¹

Affiliation:

1. Department of Chemistry and Biochemistry, University of California, Los Angeles, 607 Charles E. Young Drive, Los Angeles, California 90095-1569, Laboratory for Bioorganic Chemistry, Sloan-Kettering Institute for Cancer Research, 1275 York Avenue, New York, New York 10065, and Department of Chemistry, Columbia University, Havemeyer Hall, 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/ja1009162

Reference42 articles.

1. Improved Dienophilicity of Nitrocycloalkenes: Prospects for the Development of a trans-Diels−Alder Paradigm

2. Tandem [4+2]/[3+2] Cycloadditions of Nitroalkenes

3. Inter- and intramolecular [4 + 2] cycloadditions of nitroalkenes with olefins. 2-Nitrostyrenes

4. Intermolecular [4 + 2]-Cycloadditions of Nitroalkenes with Cyclic Olefins. Transformations of Cyclic Nitronates

5. The stereostructures of [1,1′-bicyclohexyl]-2,2′-diones: A reassignment

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