152141-30-5Relevant academic research and scientific papers
Glycosylation mediated - BAIL in aqueous solution
Delacroix, Sébastien,Bonnet, Jean-Pierre,Courty, Matthieu,Postel, Denis,Van Nhien, Albert Nguyen
, p. 12 - 18 (2013/10/08)
The use of Br?nsted acid ionic liquid (BAIL) as a catalyst for the activation of unreactive and unprotected glycosyl donors has been demonstrated for the first time in aqueous solution.
Efficient glycosylation of unprotected sugars using sulfamic acid: A mild eco-friendly catalyst
Guchhait, Goutam,Misra, Anup Kumar
experimental part, p. 52 - 57 (2012/01/15)
Sulfamic acid, a mild and environmentally benign catalyst has been successfully used in the Fischer glycosylation of unprotected sugars for the preparation alkyl glycosides. A diverse range of aliphatic alcohols have been used to prepare a series of alkyl glycosides in good to excellent yield.
Glycosylation using unprotected alkynyl donors
Mamidyala, Sreeman K.,Finn
experimental part, p. 8417 - 8420 (2010/01/16)
(Chemical Equation Presented) Gold(III) activation of unprotected propargyl glycosyl donors has been shown to be effective for the synthesis of saccharides. Terminal propargyl glycosides of glucose, galactose, and mannose required heating at reflux in ace
Experimental evidence on the hydroxymethyl group conformation in alkyl β-D-mannopyranosides
Mayato, Carlos,Dorta, Rosa,Vazquez, Jesus
, p. 2385 - 2397 (2007/10/03)
A rotational population study of the hydroxymethyl group of alkyl β-D-mannopyranosides was performed by means of CD and NMR spectroscopy. Three different benzyl, acetyl, and p-bromobenzoyl series of alkyl β-D-mannopyranosides with different chiral and non
