Redox Glycosidation: A New Strategy for Disaccharide Synthesis

DOI: 10.1021/ja00186a037

Source and publish data:

Journal of the American Chemical Society p. 1392 - 1396 (1989)

Update date:2022-09-26

Topics:

Authors:

Barrett, Anthony G. M.

Bezuidenhoudt, Barend C. B.

Gasiecki, Alan F.

Howell, Amy R.

Russell, Mark A.

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Article abstract of DOI:10.1021/ja00186a037

A new procedure for the preparation of disaccharides via redox glycosidation is described.The crucial anomeric C-O bond is established by acylation not alkylation as in traditional Koenigs-Knorr chemistry.Tebbe methylenylation followed by cyclization unra

Full text of DOI:10.1021/ja00186a037

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