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

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

Source and publish data:

Tetrahedron Letters p. 2613 - 2616 (1998)

Update date:2022-08-02

Topics:

Authors:

Katagiri, Nobuya

Morishita, Yoshihiro

Yamaguchi, Masahiko

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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

Full text of DOI:10.1016/S0040-4039(98)00282-2

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