Protection-free synthesis of glycosyl dithiocarbamates in aqueous media by using 2-chloroimidazolinium reagent

[1]  A. Wei,et al.  Glycosyl Dithiocarbamates: β-Selective Couplings without Auxiliary Groups , 2014, The Journal of organic chemistry.

[2]  F. Santoyo-González,et al.  Masked thiol sugars: chemical behavior and synthetic applications of S-glycopyranosyl-N-monoalkyl dithiocarbamates. , 2014, Chemistry, an Asian journal.

[3]  M. Noguchi,et al.  Direct Introduction of Detachable Fluorescent Tag into Oligosaccharides , 2013 .

[4]  M. Haiba Synthesis and Cytotoxicity of Some New Substituted Hydronaphthalene Derivatives , 2013 .

[5]  M. Noguchi,et al.  A Practical One‐Step Synthesis of 1,2‐Oxazoline Derivatives from Unprotected Sugars and Its Application to Chemoenzymatic β‐N‐Acetylglucosaminidation of Disialo‐oligosaccharide , 2012 .

[6]  R. Grainger,et al.  Radical-mediated reduction of the dithiocarbamate group under tin-free conditions. , 2012, Organic & biomolecular chemistry.

[7]  A. Wei,et al.  Glycal assembly by the in situ generation of glycosyl dithiocarbamates. , 2012, Organic letters.

[8]  M. Noguchi,et al.  Direct dehydrative pyridylthio-glycosidation of unprotected sugars in aqueous media using 2-chloro-1,3-dimethylimidazolinium chloride as a condensing agent. , 2011, Chemistry, an Asian journal.

[9]  L. Kremer,et al.  Synthesis and evaluation of anti-tubercular activity of new dithiocarbamate sugar derivatives. , 2011, Bioorganic & medicinal chemistry letters.

[10]  A. Halimehjani,et al.  Synthesis of dithiocarbamate by Markovnikov addition reaction in aqueous medium , 2010 .

[11]  Yoshifumi Yamamoto,et al.  Synthesis of new sugar derivatives and evaluation of their antibacterial activities against Mycobacterium tuberculosis. , 2009, Bioorganic & medicinal chemistry letters.

[12]  M. Noguchi,et al.  One-step conversion of unprotected sugars to beta-glycosyl azides using 2-chloroimidazolinium salt in aqueous solution. , 2009, Chemical communications.

[13]  M. Noguchi,et al.  Direct Synthesis of 1,6-Anhydro Sugars from Unprotected Glycopyranoses by Using 2-Chloro-1,3-dimethylimidazolinium Chloride , 2009 .

[14]  M. Noguchi,et al.  Direct Transformation of Unprotected Sugars to Aryl 1-Thio-β-glycosides in Aqueous Media Using 2-Chloro-1,3-dimethylimidazolinium Chloride , 2009 .

[15]  M. Noguchi,et al.  Efficient synthesis of sugar oxazolines from unprotected N-acetyl-2-amino sugars by using chloroformamidinium reagent in water. , 2009, The Journal of organic chemistry.

[16]  J. Fernández-Bolaños,et al.  cis-Fused bicyclic sugar thiocarbamates. Reactivity towards amines , 2008 .

[17]  S. Dolman,et al.  Isothiocyanates from tosyl chloride mediated decomposition of in situ generated dithiocarbamic acid salts. , 2007, The Journal of organic chemistry.

[18]  W. Szeja,et al.  Synthesis of glycofuranosides from S-glycofuranosyl dithiocarbonates (xanthates) and dithiocarbamates , 1996 .

[19]  S. Oscarson,et al.  Glycosyl 1-piperidinecarbodithioates in the synthesis of glycosides , 1991 .

[20]  N. Fukada,et al.  Reaction of carbon disulphide with cyclic amides and related compounds. Free N-acyl- and N-carbamoyl-dithiocarbamic acids , 1979 .

[21]  Setsuzo Tejima,et al.  Thiosugars. X. Studies on glycosyl N,N-dialkyldithiocarbamates. , 1967, Chemical & pharmaceutical bulletin.