96689-84-8Relevant academic research and scientific papers
2′-Carboxybenzyl glycosides: glycosyl donors for C-glycosylation and conversion into other glycosyl donors
Lee, Yong Joo,Baek, Ju Yuel,Lee, Bo-Young,Kang, Sung Soo,Park, Hye-Seo,Jeon, Heung Bae,Kim, Kwan Soo
, p. 1708 - 1716 (2007/10/03)
Glycosylation of various glycosyl acceptors with 2′-carboxybenzyl (CB) 2,3,4,6-tetra-O-benzyl-β-d-glucopyranoside and CB 2,3,4,6-tetra-O-benzyl-α-d-mannopyranoside as glycosyl donors afforded α-C-glycosides exclusively or predominantly in good yields. CB
C-GLYCOSIDATION OF PYRIDYL THIOGLYCOSIDES
Williams, Robert M.,Stewart, Andrew O.
, p. 2715 - 2718 (2007/10/02)
The pyridylthioglycosides 1 are efficiently transformed into the corresponding C-glycosides via reaction with silver(I) triflate and a variety of carbon nucleophiles.
C-Glycosylflavonoids, I. - Synthesis of 4',7-Di-O-methylisobayin
Tschesche, Rudolf,Widera, Wolfgang
, p. 902 - 907 (2007/10/02)
Reaction of 2,4-dimethoxyphenylmagnesium bromide with 2,3,4,6-tetra-O-benzylglucopyranosyl chloride in THF gave mainly 2,3,4,6-tetra-O-benzyl-1-(2,4-dimethoxyphenyl)-1-desoxy-β-D-glucopyranose (1).After cleavage of the benzyl groups and acetylation the te
