STEREOCHEMICAL CONTROL OF NATURE'S BIOSYNTHETIC PATHWAYS: A GENERAL STRATEGY FOR THE SYNTHESIS OF POLYPROPIONATE-DERIVED STRUCTURAL UNITS FROM A SINGLE CHIRAL PROGENITOR

DOI: 10.1016/S0040-4020(01)87683-3

Source and publish data:

Tetrahedron p. 5055 - 5072 (1987)

Update date:2022-08-04

Topics:

Authors:

Hanessian, S.

Murray, P. J.

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Article abstract of DOI:10.1016/S0040-4020(01)87683-3

A general strategy that permits the stereocontrolled construction of acyclic chains containing vicinal and/or alternating alkyl and hydroxy substituents is presented.Structural subunits of ionomycin were synthesized from a common chiral intermediate.

Full text of DOI:10.1016/S0040-4020(01)87683-3

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