193359-93-2

Upstream product

• 77-76-9 2,2-dimethoxy-propane 
• 193359-92-1 phenyl 1-thio-α-D-arabinopyranoside 
• 108-98-5 thiophenol 
• 107961-02-4 phenyl 2,3,4-tri-O-acetyl-1-thio-α-D-arabinopyranoside 
• 19186-37-9 1,2,3,4-tetra-O-acetyl-α-D-arabinopyranose 
• 28697-53-2 D-arabinopyranose 

Downstream Products

• 193359-94-3 (3aR,6R,7S,7aR)-7-Methoxy-2,2-dimethyl-6-phenylsulfanyl-tetrahydro-[1,3]dioxolo[4,5-c]pyran 
• 201142-47-4 (3aR,6R,7S,7aR)-7-(4-Methoxy-benzyloxy)-2,2-dimethyl-6-phenylsulfanyl-tetrahydro-[1,3]dioxolo[4,5-c]pyran 
• 201142-54-3 (Z)-2-[(2S,3S,4S,5R)-4,5-Bis-(tert-butyl-dimethyl-silanyloxy)-3-(4-methoxy-benzyloxy)-tetrahydro-pyran-2-yloxymethyl]-3-[(1S,2R,6R)-6-isopropyl-3-methyl-2-((2S,3S)-3-methyl-2,3-bis-triethylsilanyloxy-pent-4-ynyl)-cyclohex-3-enyl]-propenal 
• 201142-53-2 (Z)-2-[(2R,3S,4S,5R)-4,5-Bis-(tert-butyl-dimethyl-silanyloxy)-3-(4-methoxy-benzyloxy)-tetrahydro-pyran-2-yloxymethyl]-3-[(1S,2R,6R)-6-isopropyl-3-methyl-2-((2S,3S)-3-methyl-2,3-bis-triethylsilanyloxy-pent-4-ynyl)-cyclohex-3-enyl]-propenal 
• 213824-35-2 C₅₇H₁₀₀O₉Si₄ 
• 201142-56-5 C₅₇H₁₀₀O₉Si₄ 
• 201142-55-4 C₅₇H₁₀₂O₉Si₄ 
• 174545-76-7 eleutherobin 
• 201142-52-1 2,2,2-Trichloro-acetimidic acid (2S,3S,4S,5R)-4,5-bis-(tert-butyl-dimethyl-silanyloxy)-3-(4-methoxy-benzyloxy)-tetrahydro-pyran-2-yl ester 
• 201142-50-9 (2R,3S,4S,5R)-4,5-Bis-(tert-butyl-dimethyl-silanyloxy)-3-(4-methoxy-benzyloxy)-2-phenylsulfanyl-tetrahydro-pyran 
• 201142-49-6 (3R,4R,5S,6R)-5-(4-Methoxy-benzyloxy)-6-phenylsulfanyl-tetrahydro-pyran-3,4-diol 

Relevant academic research and scientific papers

Synthetic studies on glycosphingolipids from protostomia phyla: Synthesis of glycosphingolipid from the marine sponge Spheciospongia vesparia and its analogue

Stereocontrolled syntheses of a neutral glycosphingolipid found from a marine sponge Spheciospongia vesparia and its analogue have been accomplished. Disaccharide glycosphingolipids, β-D-Arap-(1→6)-β-D-Glcp-(1?1)-Cer (1) and α-D-Arap-(1→6)-β-D-Glcp-(1?1)-Cer (2), were synthesized from suitable monosaccharide donors and an acceptor by stepwise synthesis.

Design, synthesis and biological evaluation of carbohydrate-based mimetics of cRGDFV

The design, synthesis and preliminary biological evaluation of carbohydrate-based non-peptide mimetics of the potent peptidic antagonist of α(v)β3 and α(v)β5, pentapeptide cRGDFV (1) is presented. The design was based on the NMR-determined structure of 1.