An efficient method for the synthesis of aromatic C-nucleosides

DOI: 10.1016/0040-4039(95)00145-3

Source and publish data:

Tetrahedron Letters p. 1795 - 1798 (1995)

Update date:2022-09-26

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Authors:

Chaudhuri, Narayan C.

Kool, Eric T.

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Article abstract of DOI:10.1016/0040-4039(95)00145-3

Reaction of diarylcadmium or diarylzinc reagents with 1,2-dideoxy-3,5-di-O-p-toluoyl-1-chloro-α-D-ribofuranose affords 3,5-di-O-protected aromatic C-nucleosides in good yields.

Full text of DOI:10.1016/0040-4039(95)00145-3

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