Tandem Inter [4 + 2]/Intra [3 + 2] Cycloadditions of Nitroalkenes. Asymmetric Synthesis of Highly Functionalized Aminocyclopentanes Using the Bridged Mode (β-Tether) Process-Reference-Cited by-同舟云学术

Tandem Inter [4 + 2]/Intra [3 + 2] Cycloadditions of Nitroalkenes. Asymmetric Synthesis of Highly Functionalized Aminocyclopentanes Using the Bridged Mode (β-Tether) Process

Published:1998-08-21 Issue:18 Volume:63 Page:6178-6195
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Denmark Scott E.¹,Dixon Julie A.¹

Affiliation:

1. Roger Adams Laboratory, Department of Chemistry, University of Illinois, Urbana, Illinois 61801

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo9802170

Reference81 articles.

1. Catalytic asymmetric Diels Alder reactions

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

3. Tandem inter [4+2]/intra [3+2]nitroalkene cycloadditions. 5. Origin of the Lewis acid dependent reversal of stereoselectivity

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