Synthetic study on tautomycin. Stereocontrolled synthesis of C(1)-C(18) fragment using a strategy of selective reduction of spiroketal

DOI: 10.1016/S0040-4039(00)74091-3

Source and publish data:

Tetrahedron Letters p. 4797 - 4800 (1993)

Update date:2022-09-26

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Authors:

Oikawa Oikawa

Ichihara

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Article abstract of DOI:10.1016/S0040-4039(00)74091-3

A stereocontrolled synthesis of C(1)-C(18) fragment of tautomycin is accomplished employing asymmetric crotylboration, selective reduction of spiroketal, and addition of crotylstannane as the key steps.

Full text of DOI:10.1016/S0040-4039(00)74091-3

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