SYNTHETIC STUDIES ON (+)-HYDANTOCIDIN (4): SYNTHESIS OF STEREOSISOMERS OF (+)-HYDANTOCIDIN

DOI: 10.1016/S0040-4020(01)96125-3

Source and publish data:

Tetrahedron p. 2145 - 2154 (1991)

Update date:2022-08-03

Topics:

Authors:

Mio, Shigeru

Ueda, Masumi

Hamura, Masae

Kitagawa, Junko

Sugai, Soji

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Article abstract of DOI:10.1016/S0040-4020(01)96125-3

The stereoisomers of (+)-hydantocidin were synthesized by diastereoselective dihydroxylation directly or epoxidation followed by ring opening of 1-oxa-6,8-diazaspiro<4.4>nonane-3-ene-7,9-dione systems.

Full text of DOI:10.1016/S0040-4020(01)96125-3

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Product name:<2R,5R>-2-Benzyloxymethyl-8-(4-methoxybenzyl)-6-benzyloxycarbonyl-1-oxa-6,8-diazaspiro<4.4>nonane-3-ene-7,9-dione

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