Enantioselective 1,3-Dipolar Cycloaddition Reactions of C -Carboxy Ketonitrones and Enals with MacMillan Catalysts: Evidence of a Nonconcerted Mechanism-Reference-Cited by-同舟云学术

Enantioselective 1,3-Dipolar Cycloaddition Reactions of C -Carboxy Ketonitrones and Enals with MacMillan Catalysts: Evidence of a Nonconcerted Mechanism

Published:2017-12-04 Issue:45 Volume:2017 Page:6763-6774
ISSN:1434-193X
Container-title:European Journal of Organic Chemistry
language:en
Short-container-title:Eur. J. Org. Chem.

Author:

Ben Ayed Kawther¹²,Laurent Mathieu Y.¹,Martel Arnaud¹,Selim Khalid B.³,Abid Souhir²,Dujardin Gilles¹

Affiliation:

1. IMMM UMR CNRS 6283; Faculté des Sciences; Université du Maine; 72085 Le Mans France

2. Laboratoire de Chimie Appliquée; Faculté des Sciences; Faculté des Sciences, Université de Sfax; 3000 Sfax Tunisia

3. Department of Pharmaceutical Organic Chemistry; Faculty of Pharmacy, Mansoura University; 35516 Mansoura Egypt

Funder

French National Research Agency

Publisher

Wiley

Subject

Organic Chemistry,Physical and Theoretical Chemistry

Reference36 articles.

1. Isoxazolidine: A Privileged Scaffold for Organic and Medicinal Chemistry

2. Optically active isoxazolidines via asymmetric cycloaddition reactions of nitrones with alkenes: applications in organic synthesis

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