67412-72-0Relevant academic research and scientific papers
An extremely mild and general method for the construction of 1,2-trans- β-glycosidic linkages via glycopyranosyl diethyl phosphites with participating groups at C-2
Hashimoto,Sano,Umeo,Nakajima,Ikegami
, p. 2267 - 2269 (2007/10/03)
A highly efficient 1,2-trans-β-glycosidation reaction has been developed by using glycopyranosyl diethyl phosphites bearing participating groups such as benzoate, phthalimido, or trichloroethyl carbamate groups at C-2 as glycosyl donors and trimethylsilyl
An efficient construction of 1,2-trans-β-glycosidic linkages capitalizing on glycopyranosyl N,N,N',N'-tetramethylphosphoroamidates as shelf-stable glycosyl donors
Hashimoto,Yanagiya,Honda,Harada,Ikegami
, p. 3523 - 3526 (2007/10/02)
A highly stereocontrolled 1,2-trans-β-glycosidation reaction with or without neighbouring group participation has been developed by using benzyl- or benzoyl-protected glycopyranosyl N,N,N',N'-tetramethylphosphoramidates as shelf-stable glycosyl donors in
