Simultaneously Electrogenerated Cycloaddition Partners for Regiospecific Inverse-Electron-Demand Diels−Alder Reactions: A Route for Polyfunctionalized 1,4-Benzoxazine Derivatives-Reference-Cited by-同舟云学术

Simultaneously Electrogenerated Cycloaddition Partners for Regiospecific Inverse-Electron-Demand Diels−Alder Reactions: A Route for Polyfunctionalized 1,4-Benzoxazine Derivatives

Published:2004-01-13 Issue:3 Volume:69 Page:882-890
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Blattes Estelle¹,Fleury Maurice-Bernard¹,Largeron Martine¹

Affiliation:

1. UMR 8638 CNRS - Université René Descartes, Synthèse et Structure de Molécules d'Intérêt Pharmacologique, Faculté des Sciences Pharmaceutiques et Biologiques, 4 Avenue de l'Observatoire, 75270 Paris Cedex 06, France

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo035614b

Reference35 articles.

1. The Catalytic Enantioselective Construction of Molecules with Quaternary Carbon Stereocenters

2. A Powerful o-Quinone Dimethide Strategy for Intermolecular Diels−Alder Cycloadditions

3. Multicomponent domino reactions for the synthesis of biologically active natural products and drugs

4. The Diels-Alder Reaction in Total Synthesis

5. Paraherquamides, Brevianamides, and Asperparalines: Laboratory Synthesis and Biosynthesis. An Interim Report

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