STEREOSPECIFIC SYNTHESIS OF THE C(3)-C(10) SEGMENT OF APLASMOMYCIN FROM (R)-PULEGONE

DOI: 10.1016/S0040-4039(00)96285-3

Source and publish data:

Tetrahedron Letters p. 3061 - 3064 (1987)

Update date:2022-07-30

Topics: Stereospecific synthesis

Authors:

White, James D.

Kuo, Shen-chun

Vedananda, Thalathani R.

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Article abstract of DOI:10.1016/S0040-4039(00)96285-3

A key subunit of aplasmomycin comprising C3-C10 of the symmetrical macrodiolide structure has been synthesized in optically pure form by two routes from (R)-(+)-pulegone.

Full text of DOI:10.1016/S0040-4039(00)96285-3

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