82186-07-0Relevant academic research and scientific papers
Tuneable regioselectivity during the mono-etherification of the 2,3-diol of a mannose derivative This paper is dedicated to the memory of the late Dr. John M. Webber, distinguished carbohydrate chemist and founding editor of Carbohydrate Research
Petursson, Sigthor,Scully, Sean M.,Jonsdottir, Sigridur
, p. 37 - 43 (2014/03/21)
The paper reports selective mono-etherification of the 2-, and 3-hydroxyl groups of methyl 4,6-O-isopropylidene-α-d-mannopyranoside using tin(II) chloride catalysed reactions of diaryldiazomethanes. By the use of different diazo compounds and the variatio
REGIOSELECTIVE MONOALKYLATION OF THE VICINAL cis-DIOL GROUP IN MANNOPYRANOSIDES USING DIARYLDIAZOALKANES-TIN(II) CHLORIDE
Petursson, Sigthor,wEbber, John M.
, p. 41 - 52 (2007/10/02)
Highly regioselective monoalkylations of the cis-2,3-diol group in mannopyranosides can be achieved with diaryldiazoalkanes in the presence of catalytic amounts of tin(II) chloride.With diazo(diphenyl)methane (1), its 4,4'-dimethyl (2) and 4,4'-dichloro (
