Intriguing Behavior of Cinchona Alkaloids in the Enantioselective Organocatalytic Hydroxyamination of α-Substituted-α-cyanoacetates-Reference-Cited by-同舟云学术

Intriguing Behavior of Cinchona Alkaloids in the Enantioselective Organocatalytic Hydroxyamination of α-Substituted-α-cyanoacetates

Published:2007-08-09 Issue:18 Volume:72 Page:7062-7065
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

López-Cantarero Jesús¹,Cid M. Belén¹,Poulsen Thomas B.¹,Bella Marco¹,Ruano José Luis García¹,Jørgensen Karl Anker¹

Affiliation:

1. Departamento de Química Orgánica, Universidad Autónoma de Madrid, Cantoblanco, 28049-Madrid, Spain, and Danish National Research Foundation Center for Catalysis, Department of Chemistry, Aarhus University, DK-8000 Aarhus C, Denmark kaj@chem.au.dk

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo071186o

Reference40 articles.

1. The Nitroso Ene Reaction: A Regioselective and Stereoselective Allylic Nitrogen Functionalization of Mechanistic Delight and Synthetic Potential

2. Catalytic Enantioselective Synthesis of α-Aminooxy and α-Hydroxy Ketone Using Nitrosobenzene

3. Enantioselective O- and N-Nitroso Aldol Synthesis of Tin Enolates. Isolation of Three BINAP−Silver Complexes and Their Role in Regio- and Enantioselectivity

4. A Facile and Rapid Route to Highly Enantiopure 1,2-Diols by Novel Catalytic Asymmetricα-Aminoxylation of Aldehydes

5. The Direct and Enantioselective Organocatalytic α-Oxidation of Aldehydes

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