121682-61-9Relevant academic research and scientific papers
C2-Acetamidomannosylation. Synthesis of 2-N-acetylamino-2-deoxy-α-D-mannopyranosides with glucal donors
Liu, Jing,Di Bussolo, Valeria,Gin, David Y.
, p. 4015 - 4018 (2003)
A one-pot C2-acetamidomannosylation reaction for the synthesis of 2-N-acetylamino-2-deoxy-α-D-mannopyranosides from glucals is described. Glucal donors are activated by the reagent combination of 2,8-dimethyldibenzothiophene-5-oxide (DMDBTO) and trifluoromethanesulfonic anhydride. Upon subsequent addition of N-(TMS)acetamide and an appropriate glycosyl acceptor, the corresponding C2-acetamidomannopyranosides are formed.
Formation of 2-acetamido-2-deoxy-d-glucopyranosidic linkages via glycosidation using a combination of two lewis acids
Oda, Yoshiki,Midorikawa, Masanobu,Yamanoi, Takashi
, p. 198 - 215 (2015/03/04)
A mixed activation system composed of ytterbium(III) triflate and a catalytic boron trifluoride diethyl etherate complex efficiently promotes the glycosylation of various alcohol acceptors using 2-acetamido-3,4,6-tri-O-benzyl-2-deoxy-α-D-glucopyranosyl ac
A Novel Glycosylation Reaction of 2-Amino-2-deoxy-D-glucopyranose Using Dimethylphosphinothioate
Inazu, Toshiyuki,Yamanoi, Takashi
, p. 69 - 72 (2007/10/02)
β-Glucosides were stereoselectively obtained in good yields from 3,4,6-tri-O-benzyl-2-benzyloxycarbonylamino-2-deoxy-α-D-glucopyranosyl dimethylphosphinothioate with several alcohols in the presence of iodine and a catalytic amount of trityl or perchlorat
