Enantioselective Protonation of Silyl Enol Ethers and Ketene Disilyl Acetals with Lewis Acid-Assisted Chiral Brønsted Acids: Reaction Scope and Mechanistic Insights-Reference-Cited by-同舟云学术

Enantioselective Protonation of Silyl Enol Ethers and Ketene Disilyl Acetals with Lewis Acid-Assisted Chiral Brønsted Acids: Reaction Scope and Mechanistic Insights

Published:2000-08-01 Issue:34 Volume:122 Page:8120-8130
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Nakamura Shingo¹,Kaneeda Masanobu¹,Ishihara Kazuaki¹,Yamamoto Hisashi¹

Affiliation:

1. Contribution from the Graduate School of Engineering, CREST, Japan Science and Technology Corporation (JST), and Research Center for Advanced Waste and Emission Management (ResCWE), Nagoya University, Furo-cho, Chikusa, Nagoya 464-8603, Japan

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja001164i

Reference59 articles.

1. Deracemization via Highly Enantioselective Enolate Protonation Using a Chiral Aniline as the "Acid"

2. Enzyme-mediated enantioface-differentiating hydrolysis of .alpha.-substituted cycloalkanone enol esters

3. Enzyme-mediated enantioface-differentiating hydrolysis of α-substituted sulfur-containing cyclic ketone enol esters

4. (c) Katoh, O.; Sugai, T.; Ohta, H.Tetrahedron: Asymmetry1994,5, 1935.

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