612844-12-9Relevant academic research and scientific papers
Di-tert-butylsilylene (DTBS) group-directed α-selective galactosylation unaffected by C-2 participating functionalities
Imamura, Akihiro,Ando, Hiromune,Korogi, Satomi,Tanabe, Genzoh,Muraoka, Osamu,Ishida, Hideharu,Kiso, Makoto
, p. 6725 - 6728 (2003)
We have discovered an unusual α-galactosylation using phenylthioglycoside of 4,6-O-di-tert-butylsilylene (DTBS)-protected galactose derivatives as a glycosyl donor, which was not hampered by the neighboring participation of C-2 acyl functionality such as NTroc and OBz. The power of the DTBS effect has been exemplified by the coupling reaction with various glycosyl acceptors.
Ganglioside GQ1b: Efficient total synthesis and the expansion to synthetic derivatives to elucidate its biological roles
Imamura, Akihiro,Ando, Hiromune,Ishida, Hideharu,Kiso, Makoto
supporting information; experimental part, p. 3009 - 3023 (2009/08/15)
The convergent total synthesis of ganglioside GQ1b based on the "cassette approach" between the nonreducing end GQ1b-core heptasaccharide and glucosylceramide building blocks was accomplished in high overall yield. The use of a sialylα(2→8)sialylα(2→3) ga
