96689-88-2Relevant academic research and scientific papers
An efficient glycosylation reaction of 1-hydroxy sugars with various nucleophiles using a catalytic amount of activator and hexamethyldisiloxane
Mukaiyama,Matsubara,Hora
, p. 1368 - 1373 (1994)
In the presence of hexamethyldisiloxane and anhydrous calcium sulfate, a catalytic amount of activator such as tin(II) trifluoromethanesulfonate, ytterbium trifluoromethanesulfonate, lanthanum trifluoromethanesulfonate or tin(II) chloride smoothly promote
New Entry to the C-Glycosilation by means of Carbenoid Displacement Reaction. Its Application to the Synthesis of Showdomycin
Kametani, Tetsuji,Kawamura, Kuniaki,Honda, Toshio
, p. 3010 - 3017 (2007/10/02)
The novel and stereoselective carbon-carbon bond-forming reaction at the anomeric center of carbohydrates has been developed by means of a carbenoid displacement reaction with phenyl thioglycosides.This reaction was suggested to proceed via the oxonium ion intermediates and has the following advantages: (i) the preferential participation of a carbenoid with a sulfur atom can restrict the reaction site; (ii) the reaction can be carried out under neutral reaction condition; and (iii) the introduction of various functionalities can be accomplished by manipulation of the organosulfur groups of the products.This synthetic strategy was successfully applied to the synthesis of antitumor agent, (+)-showdomycin, and would provide a general route to the other C-glycosides.
