106444-73-9

Upstream product

• 58341-56-3 methyl 3-O-allyl-2-O-benzyl-4,6-O-benzylidene-α-D-mannopyranoside 
• 100-39-0 benzyl bromide 
• 82228-10-2 methyl 3-O-allyl-4,6-O-benzylidene-α-D-mannopyranoside 
• 73045-61-1 methyl 3-O-allyl-2,4,6-tri-O-benzyl-α-D-mannopyranoside 

Relevant academic research and scientific papers

An easy and versatile approach for the regioselective De-O-benzylation of protected sugars based on the I2/Et3SiH combined system

The use of cheap and easy to handle reagents, such as I2 and Et3SiH, at low temperature allows the regioselective removal of benzyl protecting groups from highly O-benzylated carbohydrates. The observed regioselectivity is dependent

Substrates for the differentiation of the N-acetylglucosaminyltransferases. Synthesis of βDGlcNAc(->2)αDMan(1->6)βDMan and βDGlcNAc(1->2)αDMan(1->6)3)βDMan glycosides

The trisaccharide βDGlcNAc(1->2)αDMan(1->6)βDMan (2) and the tetrasaccharide βDGlcNAc(1->2)αDMan(1->6)αDMan(1->3)>βDMan (3) have been chemically synthesized as their 8-methoxycarbonyloctyl glycosides.Compounds 2 and 3, both partial structures of naturally