The Proline-Catalyzed Direct Asymmetric Three-Component Mannich Reaction: Scope, Optimization, and Application to the Highly Enantioselective Synthesis of 1,2-Amino Alcohols-Reference-Cited by-同舟云学术

The Proline-Catalyzed Direct Asymmetric Three-Component Mannich Reaction: Scope, Optimization, and Application to the Highly Enantioselective Synthesis of 1,2-Amino Alcohols

Published:2002-01-10 Issue:5 Volume:124 Page:827-833
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

List Benjamin¹,Pojarliev Peter¹,Biller William T.¹,Martin Harry J.¹

Affiliation:

1. Contribution from the Departments of Molecular Biology and Chemistry, The Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, California 92037

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja0174231

Reference61 articles.

1. Ueber ein Kondensationsprodukt aus Formaldehyd, Ammoniak und Antipyrin

2. Synthesis of diastereo- and enantiomerically pure α-amino-γ-oxo acid esters by reaction of acyliminoacetates with enamines derived from 6-membered ketones

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