Enantioselective Mannich-Type Reactions Using a Novel Chiral Zirconium Catalyst for the Synthesis of Optically Active β-Amino Acid Derivatives-Reference-Cited by-同舟云学术

Enantioselective Mannich-Type Reactions Using a Novel Chiral Zirconium Catalyst for the Synthesis of Optically Active β-Amino Acid Derivatives

Published:2000-08-01 Issue:34 Volume:122 Page:8180-8186
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Ishitani Haruro¹,Ueno Masaharu¹,Kobayashi Shū¹

Affiliation:

1. Contribution from the Graduate School of Pharmaceutical Sciences, The University of Tokyo, CREST, Japan Science and Technology Corporation (JST), Hongo, Bunkyo-ku, Tokyo 113-0033, Japan

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja001642p

Reference27 articles.

1. The Bimolecular Aliphatic Mannich and Related Reactions

2. Switchover of diastereofacial selectivity in the condensation reaction of optically active N-sulfinimine with ester enolate

3. A Ternary Complex Reagent for an Asymmetric Reaction of Lithium Ester Enolates with Imines

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