PREPARATION DES METHYL-4 HEPTANOLS-3 ERYTHRO ET THREO OPTIQUEMENT PURS.

DOI: 10.1016/S0040-4039(00)71485-7

Source and publish data:

Tetrahedron Letters p. 2057 - 2060 (1980)

Update date:2022-08-05

Topics: Preparation

Authors:

Vigneron, J. P.

Meric, R.

Dhaenens, M.

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Article abstract of DOI:10.1016/S0040-4039(00)71485-7

Optically pure enantiomers of threo and erythro 4-methylheptan-3 ols are synthesized from optically active butenolides 2 and 3 obtained via an asymmetric synthesis of propargylic carbinols.

Full text of DOI:10.1016/S0040-4039(00)71485-7

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