Asymmetric aldol and alkylation reactions mediated by the “quat” chiral auxiliary (R)-(−)-5-methyl-3,3-dimethyl-2-pyrrolidinone-Reference-Cited by-同舟云学术

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Asymmetric aldol and alkylation reactions mediated by the “quat” chiral auxiliary (R)-(−)-5-methyl-3,3-dimethyl-2-pyrrolidinone

Published:1994-04 Issue:15 Volume:35 Page:2373-2376
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Davies Stephen G.,Doisneau Gilles J.-M.,Prodger Jeremy C.,Sanganee Hitesh J.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference11 articles.

1. DIASTEREOSELECTIVE ALDOL CONDENSATION USING A CHIRAL OXAZOLIDINONE AUXILIARY: (2S,3S)-3-HYDROXY-3-PHENYL-2-METHYLPROPANOIC ACID

2. Acyclic stereoselection. 4. Assignment of stereostructure to .beta.-hydroxycarbonyl compounds by carbon-13 nuclear magnetic resonance

3. Asymmetric synthesis of chiral organosulfur compounds using N-sulfinyloxazolidinones

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