760987-75-5

Upstream product

• 760987-74-4 1-O-allyl-3,4,5-tri-O-benzyl-2-O-(4-bromobenzyl)-D-myo-inositol 
• 202845-42-9 1-O-allyl-3,4,5-tri-O-benzyl-D-myo-inositol 

Downstream Products

• 760987-43-7 (2-azido-3,4,6-tri-O-benzyl-2-deoxy-α-D-glucopyranosyl)-(1->6)-1-O-allyl-3,4,5-tri-O-benzyl-2-O-(4-bromobenzyl)-D-myo-inositol 
• 760987-76-6 (2-azido-3,4,6-tri-O-benzyl-2-deoxy-α-D-glucopyranosyl)-(1->6)-1-O-allyl-3,4,5-tri-O-benzyl-2-O-hexadecanoyl-D-myo-inositol 
• 760987-56-2 (2-azido-3,4,6-tri-O-benzyl-2-deoxy-α-D-glucopyranosyl)-(1->6)-3,4,5-tri-O-benzyl-2-O-hexadecanoyl-D-myo-inositol 
• 1053696-21-1 (2R,3R,4R,5S,6R)-2-[(1S,2R,3S,4S,5R,6S)-2-Allyloxy-4,5,6-tris-benzyloxy-3-(3',4'-dimethoxy-biphenyl-4-ylmethoxy)-cyclohexyloxy]-3-azido-4,5-bis-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran 
• 760987-55-1 O-(2-azido-3,4,6-tri-O-benzyl-2-deoxy-α-D-glucopyranosyl)-(1->6)-1-O-allyl-3,4,6-tri-O-benzyl-D-myo-inositol 

Relevant academic research and scientific papers

A Suzuki-Miyaura coupling mediated deprotection as key to the synthesis of a fully lipidated malarial GPI disaccharide

Ligandless palladium-catalyzed Suzuki-Miyaura coupling converted an inert p-bromobenzyl ether to a DDQ-labile p-(3,4-dimethoxyphenyl) benzyl ether in the presence of azide functionality and this strategy serves as a key step for the convergent synthesis of a fully lipidated malaria GPI disaccharide.