Fragmentation and wittig olefination of glucosamine derivatives-a simple route to open chain amino sugars and chiral glycerols
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[1] A. Vasella,et al. A new synthesis of N‐acetylneuraminic acid , 1988 .
[2] K. Sandhoff,et al. Diastereoselektive synthese von funktionalisierten C-α- und -β-glykosylderivaten der 2-acetamido-2-desoxy-d-glucose☆ , 1987 .
[3] R. Schmidt,et al. Synthesis of d-erythro-sphingosines☆ , 1986 .
[4] Y. Bigot,et al. A Simplified Wittig Synthesis Using a Solid-Liquid Transfer Process: V - The use of Formamide as Catalyst for the Synthesis of Alkenes From Carbonyl Compounds , 1985 .
[5] P. Hagel,et al. Removal of sugar dithioacetal group with N-bromosuccinimide , 1984 .
[6] T. D. Inch. Formation of convenient chiral intermediates from carbohydrates and their use in synthesis , 1984 .
[7] P. Rollin,et al. Structure du chromogène i de la éaction de morgan—eljon , 1977 .
[8] N. A. Sörensen,et al. Synthesis of Some 4,6-O-Alkylidene and 4,6-O-Arylidene Derivatives of 2-Acetamido-2-deoxy-D-glucose. , 1970 .
[9] T. Komano,et al. Debenzyloxycarbonylation of 1,3,4,6-Tetra-O-acetyl-2-benzyloxycarbonylamino- 2-deoxy-D-hexopyranoses in the Conversion of α,β-Acetoxy to Glycosyl Bromide , 1961 .