855306-48-8Relevant articles and documents
Enhanced diastereoselectivity in β-mannopyranosylation through the use of sterically minimal propargyl ether protecting groups
Crich, David,Jayalath, Prasanna,Hutton, Thomas K.
, p. 3064 - 3070 (2007/10/03)
2-O-Propargyl ethers are shown to be advantageous in the 4,6-O-benzylidene acetal directed β-mannosylation reaction. The effect is most pronounced when the O3 protecting group is a bulky silyl ether or a glycosidic bond; however, even with a 3-O-benzyl et