ENANTIOSPECIFIC SYNTHESIS OF A DIFFERENTIALLY PROTECTED L-CHIRO-INOSITOL FROM D-XYLOSE

Authors
KORNIENKO A DALARCAO M
Citation
A. Kornienko et M. Dalarcao, ENANTIOSPECIFIC SYNTHESIS OF A DIFFERENTIALLY PROTECTED L-CHIRO-INOSITOL FROM D-XYLOSE, Tetrahedron letters, 38(37), 1997, pp. 6497-6500
Citations number
33
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
Tetrahedron letters → ACNP
ISSN journal
00404039
Volume
38
Issue
37
Year of publication
1997
Pages
6497 - 6500
Database
ISI
SICI code
0040-4039(1997)38:37<6497:ESOADP>2.0.ZU;2-4
Abstract
A convenient synthesis of differentially protected L-chiro-inositol 7 from 2,3,4-tri-O-benzyl-D-xylopyranose is described The structure of 7 was confirmed by its transformation to the pentabenzylated derivative of (-)-quebrachitol. (C) 1997 Elsevier Science Ltd.