Litjens, Remy E. J. N. published the artcileSulfonium triflate mediated glycosidations of aryl 2-azido-2-deoxy-1-thio-D-mannosides, Category: piperidines, the publication is European Journal of Organic Chemistry (2005), 918-924, database is CAplus.
The effectiveness in terms of yield and stereoselectivity of (phenylsulfinyl)piperidine (BSP)/ trifluoromethanesulfonic anhydride (Tf2O) and di-Ph sulfoxide (DPS)/ Tf2O-mediated glycosidations of 2-azido-3-O-benzyl-4,6-O-benzylidene-2-deoxy-D-thiomannosides is described. Application of the BSP/Tf2O activator led to productive condensations using p-methoxyphenyl 2-azido-3-O-benzyl-4,6-O-benzylidene-2-deoxy-D-thiomannoside as a donor, while the more powerful DPS/Tf2O combination gave similar results using both p-methoxyphenyl and Ph 2-azido-3-O-benzyl-4,6-O-benzylidene-2-deoxy-D-thiomannosides.
European Journal of Organic Chemistry published new progress about 4972-31-0. 4972-31-0 belongs to piperidines, auxiliary class Piperidine,Benzene, name is 1-(Phenylsulfinyl)piperidine, and the molecular formula is C11H15NOS, Category: piperidines.
Referemce:
https://en.wikipedia.org/wiki/Piperidine,
Piperidine | C5H11N – PubChem