Access to enantiopure ribosyl-diazepanone core of liposidomycins

DOI: 10.1016/S0040-4039(97)10597-4

Source and publish data:

Tetrahedron Letters p. 385 - 388 (1998)

Update date:2022-08-03

Topics:

Authors:

Le Merrer, Yves

Gravier-Pelletier, Christine

Gerrouache, Mohamed

Depezay, Jean-Claude

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Article abstract of DOI:10.1016/S0040-4039(97)10597-4

A convergent synthesis of the ribosyl-diazepanone core of liposidomycins, new nucleoside antibiotics, has been carried out via enantiomerically pure epoxide and α-ribosyl aminoacid, chiral key intermediates obtained from L-ascorbic acid and D-ribose, respectively.

Full text of DOI:10.1016/S0040-4039(97)10597-4

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