On the stereoselectivity of the α-alkylation of β-hydroxy esters. Enantioselective synthesis of 4,4- and 6,6-disubstituted cyclohex-2-en-1-ones.-Reference-Cited by-同舟云学术

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On the stereoselectivity of the α-alkylation of β-hydroxy esters. Enantioselective synthesis of 4,4- and 6,6-disubstituted cyclohex-2-en-1-ones.

Published:1981-01 Issue:5 Volume:22 Page:425-428
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Fráter György

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference8 articles.

1. Regioselective intramolecular asymmetric cyclization of symmetrical open chain triketone

2. W. Kreiser & P. Below, accompanying paper

3. Über die Stereospezifität der α-Alkylierung von β-Hydroxycarbonsäureestern. Vorläufige Mitteilung

4. Oxidation of β hydroxy ester dianions: A new strategy for epoxide formation

5. Herstellung vonerythro-2-Hydroxybernsteinsäure-Derivaten aus Äpfelsäureester. Vorläufige Mitteilung

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