Origins of Regio- and Stereochemistry in Type 2 Intramolecular N-Acylnitroso Diels–Alder Reactions: A Computational Study of Tether Length and Substituent Effects-Reference-Cited by-同舟云学术

Origins of Regio- and Stereochemistry in Type 2 Intramolecular N-Acylnitroso Diels–Alder Reactions: A Computational Study of Tether Length and Substituent Effects

Published:2013-03-11 Issue:8 Volume:78 Page:4090-4098
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Cleary Leah¹,Mak Victor W.¹,Rychnovsky Scott D.¹,Shea Kenneth J.¹,Sizemore Nicholas¹

Affiliation:

1. Department of Chemistry, 1102 Natural Sciences II, University of California, Irvine, California 92697-2025, United States

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo4004025

Reference35 articles.

1. The Type 2 Intramolecular Diels-Alder Reaction: Synthesis and Chemistry of Bridgehead Alkenes

2. Intramolecular Diels-Alder reactions. A new entry into bridgehead bicyclo[3.n.1]alkenes

3. Intramolecular diels-alder cycloadditions. Synthesis of substituted derivatives of bicyclo[3.n.1]bridgehead alkenes.

4. Synthesis of the bicyclic core of the esperamicin/calichemicin class of antitumor agents

5. Further investigations of the type II diels-alder route to the bicyclic core of esperamicin/calichemicin reveal a regiochemical misassignment: Meta vs. para selectivity

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