914657-32-2

Upstream product

• 914657-29-7 2-(3',4',6'-tri-O-benzyl-β-D-glucopyranosyl)-(Z)-styrene 
• 914657-30-0 [(2S,3S,4R,5R,6R)-4,5-Bis-benzyloxy-6-benzyloxymethyl-2-((Z)-styryl)-tetrahydro-pyran-3-yloxy]-acetic acid methyl ester 
• 914657-31-1 (2R,3R,4R,5S,6S)-3,4-Bis-benzyloxy-2-benzyloxymethyl-5-(2-methoxy-allyloxy)-6-((Z)-styryl)-tetrahydro-pyran 

Downstream Products

• 914657-35-5 (1R,4R,6S,8R,9S,10S)-9,10-bis(benzyloxy)-8-benzyloxymethyl-2,7-dioxabicyclo[4.4.0]decane-4-yl methanesulfonate 
• 914657-34-4 (1R,4S,6S,8R,9S,10S)-9,10-bis(benzyloxy)-8-benzyloxymethyl-2,7-dioxabicyclo[4.4.0]decane-4-yl methanesulfonate 
• 914657-33-3 (1R,6S,8R,9S,10S)-9,10-bis(benzyloxy)-8-benzyloxymethyl-4-methoxy-2,7-dioxabicyclo[4.4.0]decane-4-one 

Relevant academic research and scientific papers

The synthesis of cis- and trans-fused bicyclic sugar amino acids

Four isomeric bicyclic sugar amino acids (SAAs) were prepared from α-acetylenic-C-glucoside 6 by employing a Petasis olefination and a ring-closing metathesis (RCM) as key steps. The applicability of the resulting SAAs in solid-phase peptide synthesis was