41093-31-6Relevant articles and documents
Facile and efficient access to C1-aminosugar derivatives under mild conditions
Gong, Ping,Guo, Chun,Guo, Mengbi,Hou, Zhuang,Wang, Xin,Wang, Yitong
supporting information, (2022/02/02)
A facile and efficient synthesis of C1-aminosugar derivatives under catalyst-free conditions is described here. In particular, readily available benzoyl glycosyl bromides react smoothly to give a broad scope of C1-aminosugar derivatives in good yields. Th
Synthesis of β-Glycosyl amides from N-glycosyl dinitrobenzenesulfonamides
Gaitonde, Vishwanath,Sucheck, Steven J.
experimental part, p. 353 - 370 (2012/07/30)
The N-glycosyl-2,4-dinitrobenzenesulfonamides were accessed via benzoyl-protected β-glycosyl azides. The azides were reduced with Adams' catalyst to the corresponding amines. The glycosylamines were sulfonated with 2,4-dinitrobenzenesulfonyl chloride to f
Selective reduction of anomeric azides to amines with tetrathiomolybdate: Synthesis of β-D-glycosylamines
Sridhar, Perali Ramu,Prabhu, Kandikere Ramaiah,Chandrasekaran, Srinivasan
, p. 5261 - 5264 (2007/10/03)
A number of β-glycosyl azide derivatives undergo reduction on treatment with tetrathiomolybdate to produce the corresponding β-D-glycosylamines exclusively without anomerization under very mild and neutral reaction conditions. Acetyl, allyl, benzoyl, and