Tetrahedron Letters p. 2085 - 2088 (1990)
Update date:2022-08-03
Topics:
Anzeveno, Peter B.
Creemer, Laura J.
(+)-Nojirimycin (1a) and (+)-1-deoxynojirimycin (2) have been prepared from 1,2-O-isopropylidene-α-D-glucofuranurono-6,3-lactone (3) by a route involving stereoselective reductive amination of 5-hydroxy-1,2-O-isopropylidene-α-D-xylo-hexofuranurono-6,3-lactone (5a).
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Doi:10.1016/S0960-894X(02)00250-0
(2002)Doi:10.1039/c5gc00062a
(2015)Doi:10.1007/BF00904696
(1964)Doi:10.1248/cpb.39.1043
(1991)Doi:10.1021/jacs.0c06139
(2020)Doi:10.1039/c4ra10842f
(2015)
