Enantioselective synthesis of beta-hydroxy-alpha-methyl-alpha-methylthio esters as precursors of anti-vic-hydroxymethyl units

Citation
I. Shiina et R. Ibuka, Enantioselective synthesis of beta-hydroxy-alpha-methyl-alpha-methylthio esters as precursors of anti-vic-hydroxymethyl units, TETRAHEDR L, 42(36), 2001, pp. 6303-6306
Citations number
42
Categorie Soggetti
Chemistry & Analysis","Organic Chemistry/Polymer Science
Journal title
TETRAHEDRON LETTERS
ISSN journal
00404039 → ACNP
Volume
42
Issue
36
Year of publication
2001
Pages
6303 - 6306
Database
ISI
SICI code
0040-4039(20010903)42:36<6303:ESOBE>2.0.ZU;2-D
Abstract
A new method for the synthesis of optically active anti-vic-hydroxymethyl u nits that correspond to anti-aldol derivatives is developed by way of succe ssive enantioselective aldol and diastereoselective desulfurization reactio ns. (C) 2001 Elsevier Science Ltd. All rights reserved.