223263-24-9

Upstream product

• 3879-79-6 (2R,3R,4S,5S,6S)-3,4,5-tris(benzyloxy)-2-((benzyloxy)methyl)-6-methoxytetrahydro-2H-pyran 
• 194410-25-8 9-O-acetyl-4,8-anhydro-5,6,7-tri-O-benzyl-1,2,3-trideoxy-D-glycero-D-galacto-non-1-enitol 

Downstream Products

• 319432-66-1 (Z)-(1R,10R,11R,12R,13R)-11,12,13-Tris-benzyloxy-3,14-dioxa-bicyclo[8.3.1]tetradec-7-en-4-one 
• 319432-69-4 (Z)-6-((2R,3R,4R,5R,6R)-3,4,5-Tris-benzyloxy-6-hydroxymethyl-tetrahydro-pyran-2-yl)-hex-4-enoic acid methyl ester 
• 302594-72-5 Phthalic acid bis-((2R,3R,4R,5R,6R)-6-allyl-3,4,5-tris-benzyloxy-tetrahydro-pyran-2-ylmethyl) ester 
• 302594-70-3 Pentanedioic acid bis-((2R,3R,4R,5R,6R)-6-allyl-3,4,5-tris-benzyloxy-tetrahydro-pyran-2-ylmethyl) ester 
• 302594-71-4 Succinic acid bis-((2R,3R,4R,5R,6R)-6-allyl-3,4,5-tris-benzyloxy-tetrahydro-pyran-2-ylmethyl) ester 
• 319432-61-6 Pent-4-enoic acid (2R,3R,4R,5R,6R)-6-allyl-3,4,5-tris-benzyloxy-tetrahydro-pyran-2-ylmethyl ester 
• 302594-69-0 Pentanedioic acid mono-((2R,3R,4R,5R,6R)-6-allyl-3,4,5-tris-benzyloxy-tetrahydro-pyran-2-ylmethyl) ester 
• 194980-05-7 3-(6-O-hexadecanyl-2,3,4-tri-O-benzyl-α-D-mannopyranosyl)propene 
• 194980-11-5 (S)-2-[2-((2R,3R,4R,5R,6R)-3,4,5-Tris-benzyloxy-6-hexadecyloxymethyl-tetrahydro-pyran-2-yl)-acetylamino]-pentanedioic acid dibenzyl ester 
• 194980-13-7 3-[2-((2R,3R,4R,5R,6R)-3,4,5-Tris-benzyloxy-6-hexadecyloxymethyl-tetrahydro-pyran-2-yl)-acetylamino]-benzoic acid ethyl ester 
• 865714-47-2 3-[2-((2R,3R,4R,5R,6R)-3,4,5-Tris-benzyloxy-6-hexadecyloxymethyl-tetrahydro-pyran-2-yl)-acetylamino]-benzoic acid 
• 194980-03-5 ((2R,3R,4R,5R,6R)-3,4,5-Tris-benzyloxy-6-hexadecyloxymethyl-tetrahydro-pyran-2-yl)-acetic acid 

Relevant academic research and scientific papers

Ring-closing olefin metathesis of prearranged C-allyl saccharides for the synthesis of C-butenyl linked homo- and hetero-disaccharides

Synthesis of C-butenyl-linked homo- and hetero-disaccharides was achieved via ring-closing olefin metathesis employing the Grubb's catalyst. (C) 2000 Elsevier Science Ltd.

Small molecules as structural and functional mimics of sialyl Lewis X tetrasaccharide in selectin inhibition: A remarkable enhancement of inhibition by additional negative charge and/or hydrophobic group

Several sialyl Lewis X (SLe(X))) mimics that contain the essential functional groups for receptor interaction and a negative charge or a hydrophobic group have been developed as inhibitors of E-, P-, and L-selectins. Some of the mimics exhibit selectin in