74808-16-5Relevant academic research and scientific papers
An extremely mild and general method for the stereocontrolled construction of 1,2-cis-glycosidic linkages via S-glycopyranosyl phosphorodiamidimidothioates
Hashimoto, Shun-Ichi,Honda, Takeshi,Ikegami, Shiro
, p. 4769 - 4772 (2007/10/02)
A highly stereocontrolled construction of 1,2-cis-glycosidic linkages under extremely mild reaction conditions has been developed by using S-glycopyranosyl N,N,N′,N′-tetramethyl-N-phenylphosphorodiamidimidothioates with a non-participating O-2-benzyl grou
A MILD AND RAPID 1,2-TRANS-GLYCOSIDATION METHOD VIA BENZOYL-PROTECTED GLYCOPYRANOSYL P,P-DIPHENYL-N-(p-TOLUENESULFONYL)PHOSPHINIMIDATES
Hashimoto, Shun-ichi,Honda, Takeshi,Ikegami, Shiro
, p. 775 - 778 (2007/10/02)
A highly efficient 1,2-trans-glycosidation reaction with a range of acid-labile alcohols has been developed by employing benzoyl-protected glycopyranosyl P,P-diphenyl-N-(p-toluenesulfonyl)phosphinimidates as glycosyl donors.
A Rapid and Efficient Synthesis of 1,2-trans-β-Linked Glycosides via Benzyl- or Benzoyl-protected Glycopyranosyl Phosphates
Hashimoto, Shun-ichi,Honda, Takeshi,Ikegami, Shiro
, p. 685 - 687 (2007/10/02)
A highly stereocontrolled construction of 1,2-trans-β-glycosidic linkage with or without neighbouring-group participation has been achieved using benzyl- or benzoyl-protected glycopyranosyl phosphates as glycosyl donors in the presence of trimethylsilyl t
