Synthesis and enzyme-inhibitory activity of methyl acarviosin analogues having the α-manno configuration

DOI: 10.1016/0008-6215(92)84056-X

Source and publish data:

Carbohydrate Research p. 79 - 90 (1992)

Update date:2022-08-03

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Authors:

Ogawa, Seiichiro

Nakamura, Yoshikazu

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Article abstract of DOI:10.1016/0008-6215(92)84056-X

Two methyl acarviosin analogues 3a and 4a, having the α-manno configuration, and their dihydro derivatives 6a and 7a were synthesized by coupling the protected pseudo-sugar epoxides with methyl 4-amino-4-deoxy- and -4,6-dideoxy-α-D-mannopyranoside.Similar

Full text of DOI:10.1016/0008-6215(92)84056-X

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Product name:Methyl 2,3-di-O-acetyl-4,6-dideoxy-4-<(1S)-(1,4/2,3,5)-2,3,4-triacetoxy-5-(acetoxymethyl)-1-cyclohexylamino>-α-D-mannopyranoside

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