Carbohydrates as Nucleophiles in Conjugate Addition for Preparation of Muramic Acid Analogues

DOI: 10.1016/S0957-4166(00)80384-5

Source and publish data:

Tetrahedron Asymmetry p. 2339 - 2350 (1994)

Update date:2022-09-26

Topics: Synthesis nucleophiles Conjugate addition Analogues Preparation Carbohydrates Experiment Reactant Muramic acid

Authors:

Becker, Bernd

Thiem, Joachim

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Article abstract of DOI:10.1016/S0957-4166(00)80384-5

Benzyl 2-acetamido-6-O-benzyl-3-O-<(S)-1-carboxy-isopropyl>-α-D-glucopyranoside (15) was synthesized stereoselectively by conjugate addition reaction, starting from benzyl 2-acetamido-6-O-benzyl-2-deoxy-α-D-glucopyranoside (9) and crotonic acid ethyl este

Full text of DOI:10.1016/S0957-4166(00)80384-5

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