85339-00-0Relevant academic research and scientific papers
New class of alkynyl glycoside analogues as tyrosinase inhibitors
Saehlim, Natthiya,Athipornchai, Anan,Sirion, Uthaiwan,Saeeng, Rungnapha
supporting information, (2020/06/01)
A new series of alkynyl glycoside analogues were designed and synthesized from cheap and a commercially available sugar by introduction of various alkynyl and alkyl groups at C-1 and C-6 positions of the sugar ring. The inhibitory abilities of alkynyl gly
STANNOUS TRIFLATE MEDIATED GLYCOSIDATIONS. A STEREOSELECTIVE SYNTHESIS OF β-D-GLUCOSIDES.
Lubineau, Andre,Malleron, Annie
, p. 1713 - 1716 (2007/10/02)
Various 1,2 trans, β-D-linked disaccharides with glucose as non-reducing unit have been prepared with complete stereoselectivity from acetobromoglucose and suitably protected sugar derivatives using stannous triflate as promoter.
Synthesis of the T-antigen trisaccharide O-beta-D-galactopyranosyl-(1 to 3)-O-(2-acetamido-2-deoxy-alpha-D-galactopyranosyl)-(1 to 6)-D-galactopyranose and O-beta-D-galactopyranosyl-(1 to 3)-O-(2-acetamido-2-deoxy-alpha-D-galacopyranosyl)-(1 to 6)-D-gluco
Paulsen,Paal
, p. 203 - 218 (2007/10/02)
The synthesis of the trisaccharides O-beta-D-galactopyranosyl-(1 to 3)-O-(2-acetamido-2-deoxy-alpha-D-galactopyranosyl)-(1 to 6)-D-galactopyranose (15) and O-beta-D-galactopyranosyl-(1 to 3)-O-(2-acetamido-2-deoxy-alpha-D-galactopyranosyl)-(1 to 6)-D-gluc
