104048-29-5Relevant academic research and scientific papers
An extremely mild and stereocontrolled construction of 1,2-cis-α-glycosidic linkages via benzyl-protected glycopyranosyl diethyl phosphites
Tanaka, Hiroko,Sakamoto, Hiroki,Sano, Ai,Nakamura, Seiichi,Nakajima, Makoto,Hashimoto, Shunichi
, p. 1259 - 1260 (2007/10/03)
A highly stereocontrolled 1,2-cis-α-glycosidation reaction under conditions mild enough for acid-labile alcohols has been developed using benzyl-protected glycopyranosyl diethyl phosphites as glycosyl donors in the presence of 2,6-di-tert-butylpyridinium
CARDIAC GLYCOSIDES: 5. STEREOSELECTIVE SYNTHESES OF DIGITOXIGENIN α-D, β-D, α-L AND β-L-GLUCOSIDES
Rathore, Hargovind,Hashimoto, Toshihiro,Igarashi, Kikuo,Nukaya, Haruo,Fullerton, Dwight S.
, p. 5427 - 5438 (2007/10/02)
As part of a continuing study of cardiac glycosides, stereoselective syntheses of the four possible glucosides of digitoxigenin were developed via the thermodynamically produced tetra-O-benzyl-D- and L-glucosyl α-trichloroacetaimidates 2α and 11α, and the
