125288-70-2Relevant academic research and scientific papers
HIGHLY STEREOSELECTIVE GLYCOSYLATION OF SIALIC ACID AIDED BY STEREOCONTROLLING AUXILIARIES
Ito, Yukishige,Ogawa, Tomoya
, p. 89 - 102 (2007/10/02)
α-Selective glycosylation of sialic acid was achieved by using a sialic acid donor which carries a stereocontrolling auxiliary such as selenide or sulfide group at C-3 position.
AN EFFICIENT APPROACH TO STEREOSELECTIVE GLYCOSYLATION OF N-ACETYLNEURAMINIC ACID: USE OF PHENYLSELENYL GROUP AS A STEREOCONTROLLING AUXILIARY
Ito, Yukishige,Ogawa, Tomoya
, p. 6221 - 6224 (2007/10/02)
α-Selective glycosylation of N-acetylneuraminic acid was achieved by use of the fluoride 3 which carries 3β-phenylselenyl substituent.
