ASYMMETRIC EPOXIDATION OF DIVINYL CARBINOL: A NEW APPROACH TO THE SYNTHESIS OF 2,6-DIDEOXYHEXOSES

DOI: 10.1016/S0040-4039(00)85328-9

Source and publish data:

Tetrahedron Letters p. 5791 - 5794 (1986)

Update date:2022-08-04

Topics:: Authors:

Babine, Robert E.

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Article abstract of DOI:10.1016/S0040-4039(00)85328-9

The high level of stereochemical control exhibited in the Sharpless epoxidation of prochiral divinyl alcohols has been exploited in short enantioselective syntheses of the dideoxy sugars D-digitoxose and D-olivose.

Full text of DOI:10.1016/S0040-4039(00)85328-9

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Article Doi

ASYMMETRIC EPOXIDATION OF DIVINYL CARBINOL: A NEW APPROACH TO THE SYNTHESIS OF 2,6-DIDEOXYHEXOSES

DOI: 10.1016/S0040-4039(00)85328-9

Source and publish data:

Authors:

Article abstract of DOI:10.1016/S0040-4039(00)85328-9

Full text of DOI:10.1016/S0040-4039(00)85328-9

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