Lipase-catalyzed transesterification of 2-phenyl-1-propanol with vinyl esters having aromatic ring in acyl moiety

DOI: 10.1016/S0040-4039(99)00943-0

Source and publish data:

Tetrahedron Letters p. 5223 - 5226 (1999)

Update date:2022-08-11

Topics:

Authors:

Kawasaki, Masashi

Goto, Michimasa

Kawabata, Shigeki

Kodama, Tomoko

Kometani, Tadashi

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Article abstract of DOI:10.1016/S0040-4039(99)00943-0

The highly enantioselective transesterification of 2-phenyl-1-propanol, which has not been efficiently resolved by lipase-catalyzed reactions, was attained by using either vinyl 3-(p-tolyl)propanoate or vinyl 3-(2- naphthyl)propanoate as the acyl donor.

Full text of DOI:10.1016/S0040-4039(99)00943-0

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