669763-44-4

Upstream product

• 540-38-5 p-Iodophenol 
• 604-69-3 β-D-glucose pentaacetate 
• 83-87-4 D-glucose pentaacetate 
• 18803-26-4 (4-iodo-phenoxy)-trimethylsilane 
• 604-68-2 α-D-glucopyranose peracetylate 
• 4468-72-8 phenyl 2,3,4,6-tetra-O-acetyl-β-D-glucopyranoside 

Downstream Products

• 20838-40-8 (4-iodo-phenyl)-β-D-glucopyranoside 
• 66642-78-2 4-(tetra-O-acetyl-β-D-glucopyranosyloxy)-trans-cinnamic acid methyl ester 
• 38968-01-3 (E)-1-(3,5-diacetoxy)-2-(4'-O-2,3,4,6-tetraacetyl-β-D-glucopyranosidophenyl)ethene 
• 1046451-08-4 5-(4-[2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyloxy]phenyl)-[2,2']-bithiophene 
• 1262996-42-8 5-(4-[2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyloxy]phenyl)-[2,2':5',2'']terthiophene 
• 1262996-41-7 5,5''-bis-(4-[2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyloxy]phenyl)-[2,2':5',2'']terthiophene 
• 1262996-39-3 5,5'-bis-(4-[2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyloxy]phenyl)-[2,2']-bithiophene 
• 38963-95-0 trans-resveratroloside 
• 869003-25-8 4-[(trimethylsilyl)ethynyl]phenoxy 2,3,4,6-tetra-O-acetyl-β-D-glucopyranoside 

Relevant academic research and scientific papers

C(sp3)-H Monoarylation of Methanol Enabled by a Bidentate Auxiliary

With the assistance of a practical directing group (COAQ), the first catalytic protocol for the palladium-catalyzed C(sp3)-H monoarylation of methanol has been developed, offering an invaluable synthesis means to establish extensive derivatives of crucial arylmethanol functional fragments. Furthermore, the gram-scale reaction, broad substrate scope, excellent functional group compatibility, and even the practical synthesis of medicines further demonstrate the usefulness of this strategy.

FeCl3-promoted and ultrasound-assisted synthesis of resveratrol O-derived glycoside analogs

Phenol derived O-glycosides were synthesized using a direct and convenient O-glycosidation, starting from acetylated sugars in the presence of FeCl 3, an inexpensive, mild and benign Lewis acid catalyst. The reactions were carried out under bot

Synthesis of d-glucose and l-phenylalanine substituted phenylene-thiophene oligomers

Phenylene-thiophene oligomers bearing peracetylated β-d-glucose or N-BOC-l-phenylalanine as chiral substituents were synthesized in good yields by a versatile protocol based on the Suzuki-Miyaura cross-coupling reaction. Aryl iodides bearing the chiral bi

ORGANIC THIN FILM TRANSISTORS COMPRISING THIENYL OLIGOMERS AND THEIR USE AS GASEOUS PHASE SENSORS

This invention pertains to gaseous analytes sensor devices comprising organic thin film transistor and, in particular, sensors able to perform the enantiomeric discrimination of gaseous analytes. The organic thin films are characterized by comprising a compound of formula (I).

Water soluble luminescent platinum terpyridine complexes with glycosylated acetylide and arylacetylide ligands: Photoluminescent properties and cytotoxicities

Platinum(n) terpyridine complexes with glycosylated acetylide and arylacetylide ligands bind to DNA with binding constants ～105 mol-1 dm3; the glycosylated arylacetylide complexes exhibit emission at λmax ≈ 620

Glycocinnasperimicin D Synthetic Studies: Synthesis of Cinnamoyl Glycosides via Iodination-Heck Reaction Sequence Starting from Phenyl Glycosides

A new approach for the synthesis of cinnamoyl glycoside has been developed via iodination-Heck reaction sequence starting from phenyl glycoside. Successful application of this procedure accomplished the construction of the right core structure of aminosug