STEREOSELECTIVITY IN THE FORMATION OF UNSATURATED WITTIG PRODUCTS AND STEREOSPECIFICITY IN THEIR ELECTROPHILE INDUCED CYCLIZATION TO C-GLYCOSIDES.

DOI: 10.1016/0040-4020(89)80054-7

Source and publish data:

Tetrahedron p. 269 - 276 (1989)

Update date:2022-08-04

Topics:

Authors:

Herrera, F. J. Lopez

Gonzalez, M. S. Pino

Sampedro, M. Nieto

Aciego, R. M. Dominguez

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Article abstract of DOI:10.1016/0040-4020(89)80054-7

The stereoselective synthesis of E and Z unsaturated Wittig products derivated from 2,3-O-isopropylidene-5-O-trityl-D-ribofuranose (3) and 2,3:5,6-di-O-isopropylidene-D-mannofuranose (4) was described, as well as their stereospecific cyclization induced b

Full text of DOI:10.1016/0040-4020(89)80054-7

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Product name:methyl 3,6-anhydro-2-deoxy-2-iodo-4,5-O-isopropylidene-7-O-trityl-D-glycero-D-altro-heptonate

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