Asymmetric Oxidative Nitroso-Diels–Alder Reaction of N-Arylhydroxylamines Catalyzed by a Chiral Phosphoric Acid-Reference-Cited by-同舟云学术

Asymmetric Oxidative Nitroso-Diels–Alder Reaction of N-Arylhydroxylamines Catalyzed by a Chiral Phosphoric Acid

Published:2016-06-29 Issue:21 Volume:81 Page:10154-10159
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Dumoulin Audrey¹,Masson Géraldine¹

Affiliation:

1. Institut de Chimie des Substances Naturelles, CNRS UPR 2301, Université Paris-Sud, Université Paris-Saclay, 1, av de la Terrasse, 91198 Gif-sur-Yvette Cedex, France

Funder

Centre National de la Recherche Scientifique

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.6b01256

Reference43 articles.

1. Nitroso Diels–Alder (NDA) reaction as an efficient tool for the functionalization of diene-containing natural products

2. The Asymmetric Hetero-Diels-Alder Reaction in the Syntheses of Biologically Relevant Compounds

3. The Nitrosocarbonyl Hetero-Diels-Alder Reaction as a Useful Tool for Organic Syntheses

4. Hetero Diels-Alder Reactions with Nitroso Dienophiles: Application to the Synthesis of Natural Product Derivatives

5. Nitroso and Azo Compounds in Modern Organic Synthesis: Late Blooming but Very Rich

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