A Hydrogen Bond Rationale for the Enantioselective β-Alkenylboration of Enones Catalyzed by O-Monoacyltartaric Acids-Reference-Cited by-同舟云学术

A Hydrogen Bond Rationale for the Enantioselective β-Alkenylboration of Enones Catalyzed by O-Monoacyltartaric Acids

Published:2014-07-08 Issue:14 Volume:79 Page:6754-6758
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Grimblat Nicolás¹,Sugiura Masaharu²,Pellegrinet Silvina C.¹

Affiliation:

1. Instituto de Química Rosario (CONICET), Facultad de Ciencias Bioquímicas y Farmacéuticas, Universidad Nacional de Rosario, Suipacha 531, Rosario 2000, Argentina

2. Graduate School of Pharmaceutical Sciences, Kumamoto University, 5-1 Oe-honmachi, Chuo-ku, Kumamoto 862-0973, Japan

Funder

Japan Society for the Promotion of Science

Consejo Nacional de Investigaciones Científicas y Técnicas

Agencia Nacional de Promoción Científica y Tecnológica

Fundación Josefina Prats

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo5012398

Reference35 articles.

1. Enantioselective conjugate addition of boronic acids to enones catalyzed by O-monoacyltartaric acids

2. Our groups have been working independently on this subject in recent years.Grimblat, N.; Sarotti, A. M.; Pisano, P. L.; Pellegrinet, S. C.Unpublished results.

3. Enantioselective Boronate Additions to N-Acyl Quinoliniums Catalyzed by Tartaric Acid

4. Temperature-jump study of the rate and mechanism of the boric acid-tartaric acid complexation

5. Complexation of phenylboronic acid with lactic acid. Stability constant and reaction kinetics

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