71204-44-9Relevant articles and documents
A convenient method for the synthesis of cyclic trithiocarbonates on carbohydrate scaffolds
Saeed, Muhammad,Abbas, Muhammad,Abdel-Jalil, Raid J.,Zahid, Muhammad,Voelter, Wolfgang
, p. 315 - 317 (2003)
An efficient regio- and stereoselective method for the synthesis of cyclic trithiocarbonates on carbohydrate skeleton is described. A freshly prepared solution of sodium trithiocarbonate reacts with cis-oriented epoxytriflate pentoses 7-11 to yield the co
Regioselective and Stereoselective Oxirane Ring-Openings of 2,3-Anhydropentopyranosides with Some Methyl Group Donating Organometallic Reagents
Inghardt, Tord,Frejd, Torbjoern,Magnusson, Goeran
, p. 4542 - 4548 (2007/10/02)
By the proper choice of methyl group transferring reagents organometallic (Me4AlLi, Me4AlLi/MeLi (1:1), Me2CuLi, Me3Al, Me2Mg) it is possible to selectively introduce a methyl group into the 2- or 3-position via epoxide ring-opening of four easily availab
Synthesis of Sugar Nitrates by Nucloephilic Substitution
Afza, Nighat,Malik, Abdul,Latif, Farzana,Voelter, Wolfgang
, p. 1929 - 1934 (2007/10/02)
A rapid high-yielding synthesis of sugar mono- and dinitrates has been achieved via displacement of the trifluoromethylsulfonyloxy (triflate) by the nitrate group.This procedure is mild, convenient, and does not attack highly acid-labile groups.It also do