Lithiated 4-Isopropyl-3-(methylthiomethyl)-5,5-diphenyloxazolidin-2-one: A Chiral Formyl Anion Equivalent for Enantioselective Preparations of 1,2-Diols, 2-Amino Alcohols, 2-Hydroxy Esters, and 4-Hydroxy-2-alkenoates-Reference-Cited by-同舟云学术

Lithiated 4-Isopropyl-3-(methylthiomethyl)-5,5-diphenyloxazolidin-2-one: A Chiral Formyl Anion Equivalent for Enantioselective Preparations of 1,2-Diols, 2-Amino Alcohols, 2-Hydroxy Esters, and 4-Hydroxy-2-alkenoates

Published:2001-04-12 Issue:9 Volume:66 Page:3059-3073
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Gaul Christoph¹,Schärer Kaspar¹,Seebach Dieter¹

Affiliation:

1. Laboratorium für Organische Chemie, Eidgenössische Technische Hochschule Zürich, ETH-Zentrum, Universitätstrasse 16, CH-8092 Zürich, Switzerland

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo0155254

Reference90 articles.

1. Part of the Master Thesis of K.S., ETH Zürich 2000.

2. Methods of Reactivity Umpolung

3. Chiral acyl anion equivalents: asymmetric synthesis of α-methoxytolualdehyde

4. Chiral acyl anion and enolonium ion equivalents. Asymmetric synthesis of α-methoxy-aldehydes

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