71204-44-9

Upstream product

• 358-23-6 trifluoromethylsulfonic anhydride 
• 61134-24-5 Benzyl 2,3-anhydro-α-D-ribopyranoside 

Downstream Products

• 143060-27-9 (3S,3aS,6R,7R,7aS)-6-Benzyloxy-7-hydroxy-2-oxo-hexahydro-furo[3,2-c]pyran-3-carboxylic acid ethyl ester 
• 135468-86-9 Benzyl-3,4-<(tert-butoxycarbonyl)cyanmethylen>-3,4-didesoxy-β-L-arabinopyranosid 
• 137405-03-9 Benzyl-3,4--3,4-didesoxy-β-L-arabinopyranosid 
• 109304-21-4 benzyl 2,3-anhydro-4-<(L-alanine benzyl ester)-N-yl>-4-deoxy-β-L-lyxopyranoside 
• 135514-27-1 Dibenzyl (Benzyl 2,3-Anhydro-β-L-lyxopyranoside) 4-Phosphate 
• 108292-73-5 Benzyl 2,3-Anhydro-4-<4-(tert-butyloxycarbonyl)phenylamino>-4-deoxy-β-L-lyxopyranoside 
• 124043-99-8 benzyl 2,3-anhydro-4-(tert-butoxycarbonyl)methyl-4-deoxy-β-L-lyxopyranoside 
• 95066-28-7 Benzyl 2,3-anhydro-β-L-lyxopyranoside 
• 96779-70-3 benzyl 2,3-anhydro-4-deoxy-4-fluoro-β-L-lyxopyranoside 
• 121783-18-4 benzyl β-L-arabino-hexapyranoside 3,4-(cyclic sulphate) 
• 121783-19-5 benzyl 2,3-anhydro-β-L-lyxo-hexapyranoside 4-(hydrogen sulphate) 
• 135514-24-8 Tris(benzyl 2,3-Anhydro-β-L-lyxopyranoside) 4-Phosphate 
• 78907-33-2 benzyl-2,3-anhydro-4-amino-4-desoxy-β-L-lyxopyranoside 
• 93125-72-5 Benzyl 2,3-anhydro-β-L-lyxopyranoside 4-nitrate 

Relevant academic research and scientific papers

A convenient method for the synthesis of cyclic trithiocarbonates on carbohydrate scaffolds

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

Synthesis and properties of selected 4-substituted anhydro sugars

A new class of 4-deoxy-4-([4-substituted-1-piperazinyl], [4-morpholinyl] and [4-(perhydro1,4-thiazin-4-y])])-2,3-anhydrolyxopyranosides (3a-g and 6a-g) were synthesized from epoxy triflate moities 2 and 5 and 4-substituted piperazines, morpholines and perhydro-1,4-thiazines, respectively, to test their antibacterial activity. The characterized series of new compounds was tested in vitro against E. coli ATCC11229, S. aureus ATCC6538 and C. albicans SATCC10231.

Regioselective and Stereoselective Oxirane Ring-Openings of 2,3-Anhydropentopyranosides with Some Methyl Group Donating Organometallic Reagents

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

A Convenient Synthesis of 4-Amino-4-desoxy Sugars

Displacement of the triflyl by the amino group in benzyl-2,3-anhydro-4-triflyl-pyranosides 4-6 gives with inversion the benzyl-2,3-anhydro-4-amino-4-desoxypyranosides 7-9.The triflyl group turns out to be a reactive leaving group which can be replaced by

Synthesis of Sugar Nitrates by Nucloephilic Substitution

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

C-4-Triflate Displacement by Azide in 2,3-Anhydro Sugars; a New Way to 4-Amino-4-deoxy Sugars

Displacement of the triflyl by the azido group in benzyl-2,3-anhydro-4-triflyl-α-D-pyranosides 4-6 gives with inversion the benzyl-2,3-anhydro-4-azido-4-deoxypyranosides 7-9.The triflyl group turns out to be a reactive leaving group which can be replaced