A new approach to the preparation of 2-substituted tetrahydrofurans with alpha-syn selectivity

DOI: 10.1016/S0040-4039(01)93363-5

Source and publish data:

Tetrahedron Letters p. 6829 - 6832 (1989)

Update date:2022-08-05

Topics:

Authors:

Mead Mead

Yang Yang

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Article abstract of DOI:10.1016/S0040-4039(01)93363-5

A strategy for selectively preparing 2-substituted tetrahydrofurans bearing α-syn side chain stereochemistry, based on intramolecular 2-oxetanone ring opening, has been demonstrated. A new approach to the preparation of 3,4-disubstituted 2-oxetanones is also presented.

Full text of DOI:10.1016/S0040-4039(01)93363-5

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