Chemoenzymatic preparation of enantiopure partial esters of conduritol E

DOI: 10.1016/S0957-4166(97)00233-4

Source and publish data:

Tetrahedron Asymmetry p. 2083 - 2084 (1997)

Update date:2022-07-31

Topics:

Authors:

Sanfilippo, Claudia

Patti, Angela

Piattelli, Mario

Nicolosi, Giovanni

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Article abstract of DOI:10.1016/S0957-4166(97)00233-4

Two partial esters of conduritol E, namely (2R)-hydroxy-(1R,3R,4R)-triacetoxycyclohex-5-ene and (1S,2S)-dihydroxy-(3S,4S)-diacetoxycyclohex-5-ene, have been prepared in high chemical and optical yields from 'benzene cis-glycol' diacetate via OsO_{4
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Full text of DOI:10.1016/S0957-4166(97)00233-4

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Product name:5-Cyclohexene-1,2,3,4-tetrol, 1,2-diacetate, (1S,2R,3S,4S)-

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