Intramolecular Diels–Alder Reactions of Cycloalkenones: Translation of HighEndoSelectivity toTransJunctions-Reference-Cited by-同舟云学术

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Intramolecular Diels–Alder Reactions of Cycloalkenones: Translation of HighEndoSelectivity toTransJunctions

Published:2012-09-18 Issue:38 Volume:134 Page:16080-16084
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Ross Audrey G.¹,Li Xiaohua¹,Danishefsky Samuel J.¹²

Affiliation:

1. Department of Chemistry, Columbia University, Havemeyer Hall, 3000 Broadway, New York, New York 10027, United States

2. Laboratory for Bioorganic Chemistry, Sloan-Kettering Institute for Cancer Research, 1275 York Avenue, New York, New York 10065, United States

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja307708q

Reference31 articles.

1. Catalytic Enantioselective Diels-Alder Reactions: Methods, Mechanistic Fundamentals, Pathways, and Applications

2. The Diels-Alder Reaction in Total Synthesis

3. Roush, W. R.Comprehensive organic synthesis;Pergamon Press:Oxford, 1991; Vol.5, pp513–550.

4. Recent Advances in Natural Product Synthesis by Using Intramolecular Diels−Alder Reactions

5. Cyclobutenone as a Highly Reactive Dienophile: Expanding Upon Diels−Alder Paradigms

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