DIASTEREOSELECTIVITY, DIASTEREOFACIAL SELECTIVITY AND REGIOSELECTIVITY IN THE REACTIONS OF CYNNAMYL CHLORIDE WITH ALDEHYDES MEDIATED BY TIN AND ALUMINIUM

DOI: 10.1016/0040-4020(89)80014-6

Source and publish data:

Tetrahedron p. 1029 - 1042 (1989)

Update date:2022-09-26

Topics:

Authors:

Coxon, James M.

Eyk, Stephen J. van

Steel, Peter J.

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Article abstract of DOI:10.1016/0040-4020(89)80014-6

The reaction of cinnamyl chlorie with a series of aryl and alkyl aldehydes mediated by tin and aluminium has been shown to be regioselective and threo diastereoselective.For aldehydes with chirality adjacent to the carbonyl function some diastereofacial s

Full text of DOI:10.1016/0040-4020(89)80014-6

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