SuperQuat chiral auxiliaries: design, synthesis, and utility-Reference-Cited by-同舟云学术

SuperQuat chiral auxiliaries: design, synthesis, and utility

Published:2019 Issue:6 Volume:17 Page:1322-1335
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Davies Stephen G.¹²³⁴⁵^ORCID,Fletcher Ai M.¹²³⁴⁵,Roberts Paul M.¹²³⁴⁵,Thomson James E.¹²³⁴⁵

Affiliation:

1. Department of Chemistry

2. Chemistry Research Laboratory

3. University of Oxford

4. Oxford

5. UK

Abstract

The design, synthesis and outline of some of the most common synthetic applications of the SuperQuat (4-substituted 5,5-dimethyloxazolidine-2-one) family of chiral auxiliaries, developed to address the shortcomings of the Evans (4-substituted oxazolidin-2-one) family of chiral auxiliaries, are presented.

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2019/OB/C8OB02819B

Reference83 articles.

1. Enantioselective aldol condensations. 2. Erythro-selective chiral aldol condensations via boron enolates

2. Oxazolidinones as chiral auxiliaries in asymmetric aldol reactions applied to total synthesis

3. Applications of oxazolidinones as chiral auxiliaries in the asymmetric alkylation reaction applied to total synthesis

4. Asymmetric Diels-Alder cycloaddition reactions with chiral .alpha.,.beta.-unsaturated N-acyloxazolidinones

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