ACYCLIC STEREOSELECTION. 28. USE OF STEREOSELECTIVE ALDOL METHODOLOGY IN THE TOTAL SYNTHESIS OF CLADINOSE.

DOI: 10.1016/S0040-4039(00)98496-X

Source and publish data:

Tetrahedron Letters p. 1001 - 1004 (1985)

Update date:2022-08-05

Topics:

Authors:

Heathcock, Clayton H.

Montgomery, Stephen H.

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Article abstract of DOI:10.1016/S0040-4039(00)98496-X

Reactions of (S)-2-benzyloxypropanal (4) with the lithium, magnesium, and zirconium enolates of methyl 2-methoxypropanoate (1) and with ketene acetals 2 and 3 have been studied and the stereostructures of the resulting products elucidated.The major stereo

Full text of DOI:10.1016/S0040-4039(00)98496-X

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