Diastereoselective synthesis of β-(3,4,6-tri-O-benzyl-2-deoxy-β-D- galactopyranosyl)-N-tert-butoxycarbonyl-D-alanine

DOI: 10.1016/S0040-4020(99)00306-3

Source and publish data:

Tetrahedron p. 6475 - 6482 (1999)

Update date:2022-08-05

Topics:

Authors:

Lieberknecht, Albrecht

Griesser, Helmut

Kraemer, Bernd

Bravo, Rodolfo D.

Colinas, Pedro A.

Grigera, Raul J.

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Article abstract of DOI:10.1016/S0040-4020(99)00306-3

Key steps in the synthesis of β-(3,4,6-tri-O-benzyl-2-deoxy-β-D- galactopyranosyl)-N-tert-butoxycarbonyl-D-alanine are the Wittig reaction of 2-deoxy-galactopyranosylphosphonium salt 2 and Garner aldehyde, as well as the subsequent diastereoselective hydr

Full text of DOI:10.1016/S0040-4020(99)00306-3

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Product name:β-(3,4,6-tri-O-benzyl-2-deoxy-β-D-galactopyranosyl)-N-tert-butoxycarbonyl-N,O-isopropylidene-D-alaninol

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