171192-29-3

Upstream product

• 58479-61-1 tert-butylchlorodiphenylsilane 
• 163125-38-0 (1'S,2'S)-Ethyl 3,4-O-(1',2'-dimethoxycyclohexane-1',2'-diyl)-1-thio-α-D-mannopyranoside 
• 765-87-7 cyclohexane-1,2-dione 
• 163125-34-6 1,1,2,2-tetramethoxycyclohexane 
• 7473-36-1 ethyl 1-thio-α-D-mannopyranoside 

Downstream Products

• 400835-46-3 ((1R,3R,4S,4aS,8aS,9aR,10aS)-4-Benzyloxy-3-ethylsulfanyl-8a,10a-dimethoxy-decahydro-2,9,10-trioxa-anthracen-1-ylmethoxy)-tert-butyl-diphenyl-silane 
• 189105-30-4 ethyl-2-O-benzyl-3,4-O-[1',2'-dimethoxycyclohexan-1',2'-diyl]-1-thio-α-D-mannopyranoside 
• 400835-48-5 (2R,3S,4S,5S,6R)-5-Benzyloxy-6-ethylsulfanyl-2-isobutoxymethyl-tetrahydro-pyran-3,4-diol 
• 400835-47-4 ethyl-2-O-benzyl-3,4-O-[1',2'-dimethoxycyclohexan-1',2'-diyl]-6-O-isobutyl-1-thio-α-D-mannopyranoside 
• 171192-33-9 (1'S,2'S)-Ethyl 2-O-benzoyl-3,4-O-(1',2'-dimethoxycyclohexane-1',2'-diyl)-1-thio-α-D-mannopyranoside 

Relevant academic research and scientific papers

Design, synthesis, and biological evaluation of α4β1 integrin antagonists based on β-D-mannose as rigid scaffold

A cyclic peptide role model was used for the design and synthesis of a new class of biologically active and α4-selective integrin antagonists (e.g. 1) based on β-D-mannose. These carbohydrate-based peptidomimetics were synthesized to include th

Preparation, structure, derivatisation and NMR data of cyclohexane-1,2-diacetal protected carbohydrates

Acid catalysed reaction of monosaccharides with 1,1,2,2-tetramethoxycyclohexane results in selective protection of vicinal, diequatorial, diol functionality as a cyclohexane-1,2-diacetal (CDA). This new methodology complements classical cyclic acetal prot