191332-83-9Relevant academic research and scientific papers
The benzyloxycarbonyl group: An alternative protective group in the mannose series
Morere, Alain,Menut, Chantal,Vidil, Carole,Skaanderup, Philip,Thorsen, Jesper,Roque, Jean-Pierre,Montero, Jean-Louis
, p. 175 - 178 (1997)
A procedure for the O-benzyloxycarbonylation at positions 2-4 in the mannose series is described. Starting from methyl 6-O-(4-methoxy)trityl-α-D-mannopyranoside, methyl 2,3,4-tri-O-benzyloxycarbonyl-6-O-(4-methoxy)trityl-α-D- mannopyranoside was obtained.
The benzyloxycarbonyl protective group: A good alternative to the benzyl protective group in the glycopyranoside and glycofuranoside series
Morere, Alain,Mouffouk, Fouzi,Chavis, Claude,Montero, Jean-Louis
, p. 7519 - 7522 (2007/10/03)
A procedure for the O-benzyloxycarbonylation of secondary alcohols in the glucose, galactose, mannose, ribose and deoxyribose series is described. Starting from the (4-methoxy)tritylated derivatives on the primary hydroxyl group, the fully protected compounds were obtained for the first time in high yields.
