A STEREOSELECTIVE OSMYLATION APPROACH TO POLYOXYGENATED NATURAL PRODUCTS. SYNTHESIS OF C(1)-C(7) AND C(7)-C(13) SUBUNITS OF ERYTHRONOLIDE A

DOI: 10.1016/S0040-4039(00)89042-5

Source and publish data:

Tetrahedron Letters p. 3275 - 3278 (1990)

Update date:2022-07-29

Topics:

Authors:

Kim, Young Gyu

Whang, Konghyun

Cooke, R. J.

Cha, Jin K.

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Article abstract of DOI:10.1016/S0040-4039(00)89042-5

The key synthons 2 and 3 of the erythronolide A seco acid (1) have been prepared in an enantiomerically pure form, utilizing a stereoselective osmylation of chiral hydroxy (Z,E)-diene ester 6a and subsequent hydrogenation

Full text of DOI:10.1016/S0040-4039(00)89042-5

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