The microsomal epoxide hydrolase-promoted hydrolysis of racemic isobutyl 3,4-anhydro-2,6-dideoxy-β-lyxohexopyranoside, which is easily prepared from isobutyl vinyl ether and but-3-en-2-one, occurs with very high regio-and enantio-selectivity, with kinetic resolution leading to the L-and D-forms of isobutyl β-boivinoside, both with an enantiomeric excess of at least 96%.
Autori interni: | |
Autori: | BARILI PL; BERTI G; CATELANI G |
Titolo: | HIGH DIASTEREO-SELECTIVITY AND ENANTIOSELECTIVITY IN THE ENZYMATIC-HYDROLYSIS OF A RACEMIC ANHYDRODEOXYSUGAR - A TOTALLY SYNTHETIC APPROACH TO BOTH ENANTIOMERS OF BOIVINOSE |
Anno del prodotto: | 1986 |
Digital Object Identifier (DOI): | 10.1039/c39860000007 |
Appare nelle tipologie: | 1.1 Articolo in rivista |
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