Highly regio- and enantio-selective deacylation of carbocyclic 3',5'- di-O-acyloxetanocins by lipases

Article abstract of DOI:10.1016/S0040-4039(98)00282-2

Carbocyclic (-)-3',5'-di-O-acyloxetanocin A and T were hydrolysed by lipase MY to give the corresponding carbocyclic (-)-3'-O-acyloxetanocins with high regioselectivity. Carbocyclic (±)-3',5'-di-O-acetyloxetanocin A was deacetylated by lipase MY to form t