Application of the Hofmann rearrangement in the synthesis of 3-amino sugar derivatives: preparation of some 3-tert-butoxycarbonylamino-3-cyano-3-deoxy and 3-acetamido-methyl-3-tert-butoxycarbonylamino-3-deoxy sugars-Reference-Cited by-同舟云学术

Application of the Hofmann rearrangement in the synthesis of 3-amino sugar derivatives: preparation of some 3-tert-butoxycarbonylamino-3-cyano-3-deoxy and 3-acetamido-methyl-3-tert-butoxycarbonylamino-3-deoxy sugars

Published:1991-01 Issue: Volume:209 Page:131-143
ISSN:0008-6215
Container-title:Carbohydrate Research
language:en
Short-container-title:Carbohydrate Research

Author:

Santoyo Gonzalez Francisco,Vargas Berenguel Antonio,Hernandez Mateo Fernando,Garcia Mendoza Pilar

Publisher

Elsevier BV

Subject

Organic Chemistry,Biochemistry,General Medicine,Analytical Chemistry

Reference43 articles.

1. Benzylation and Related Alkylations of α-Dimethylaminophenylacetonitrile by Means of Alkali Amides. Dehydrocyanation of Products to Form Enamines1

2. N,N-diethylaminoacetonitrile a generally useful latent acyl carbanion

3. Alkylations and acylations of .alpha.-(aryl)-4-morpholineacetonitriles (masked acyl anion equivalents) and their use in 1,4-additions

4. A cyanide promoted Michael reaction: the use of an aminonitrile as an enamine equivalent for the Michael reacton

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2. ChemInform Abstract: Application of the Hofmann Rearrangement in the Synthesis of 3-Amino Sugar Derivatives: Preparation of Some 3-tert-Butoxycarbonylamino-3- cyano-3-deoxy and 3-Acetamidomethyl-3-tert-butoxycarbonylamino-3-deoxy Sugars.;ChemInform;2010-08-22

3. Cobalt Boride;Encyclopedia of Reagents for Organic Synthesis;2001-04-15

4. Synthesis of some further C-3 branched 3-amino-2,3,6-trideoxysugars, related to daunosamine, as potential components for structurally modified anthracyclines;Carbohydrate Research;1992-12

5. Synthesis of methyl 3-amino-3,6-dideoxy-α-l-hexopyranosides branched at C-3;Carbohydrate Research;1991-01