HIGHLY REGIOSELECTIVE FUNCTIONALIZATION OF A CIS-1,2-DIOL IN THE MYOINOSITOL SERIES - APPLICATION TO THE SYNTHESIS OF 2-DEOXY-2-MERCAPTO-MYO-INOSITOL

Authors
GUIDOT JP LEGALL T
Citation
Jp. Guidot et T. Legall, HIGHLY REGIOSELECTIVE FUNCTIONALIZATION OF A CIS-1,2-DIOL IN THE MYOINOSITOL SERIES - APPLICATION TO THE SYNTHESIS OF 2-DEOXY-2-MERCAPTO-MYO-INOSITOL, Tetrahedron letters, 34(29), 1993, pp. 4647-4650
Citations number
20
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
Tetrahedron letters → ACNP
ISSN journal
00404039
Volume
34
Issue
29
Year of publication
1993
Pages
4647 - 4650
Database
ISI
SICI code
0040-4039(1993)34:29<4647:HRFOAC>2.0.ZU;2-6
Abstract
The synthesis of 2-deoxy-2-mercapto-myo-inositol is described,via a hi ghly regioselective functionalization of racemic 1,4,5,6-tetra-O-benzy l-myo-inositol.