Mechanistic Investigation of Enediyne-Connected Amino Ester Rearrangement. Theoretical Rationale for the Exclusive Preference for 1,6- or 1,5-Hydrogen Atom Transfer Depending on the Substrate. A Potential Route to Chiral Naphthoazepines-Reference-Cited by-同舟云学术

Mechanistic Investigation of Enediyne-Connected Amino Ester Rearrangement. Theoretical Rationale for the Exclusive Preference for 1,6- or 1,5-Hydrogen Atom Transfer Depending on the Substrate. A Potential Route to Chiral Naphthoazepines

Published:2012-02-29 Issue:6 Volume:77 Page:2773-2783
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Campolo Damien¹,Gaudel-Siri Anouk¹,Mondal Shovan¹,Siri Didier¹,Besson Eric¹,Vanthuyne Nicolas¹,Nechab Malek¹,Bertrand Michèle P.¹

Affiliation:

1. Institut de Chimie Radicalaire, CNRS UMR 7273, Equipes CMO and CTM, and ‡ISM2, CNRS UMR 7313, Equipe Chirosciences, Aix-Marseille Université, 13397 Cedex 20, Marseille, France

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo202580y

Reference70 articles.

1. Memory of Chirality in Cascade Rearrangements of Enediynes

2. Tandem Enyne Allene−Radical Cyclization: Low-Temperature Approaches to Benz[e]indene and Indene Compounds

3. Cascade Cyclizations via N,4-Didehydro-2-(phenylamino)pyridine Biradicals/Zwitterions Generated from Enyne−Carbodiimides

4. Synthesis and Thermolysis of Enediynyl Ethyl Ethers as Precursors of Enyne−Ketenes

5. Cascade Radical Cyclizations via Biradicals Generated from (Z)-1,2,4-Heptatrien-6-ynes

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