93135-70-7

Upstream product

• 93-58-3 benzoic acid methyl ester 
• 362-75-4 2',3'-isopropylidene adenosine 
• 98-88-4 benzoyl chloride 
• 93-97-0 benzoic acid anhydride 

Downstream Products

• 15262-12-1 ((2R,3S,4R,5R)-5-(6-amino-9H-purin-9-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methyl benzoate 
• 1174638-93-7 5'-O-benzoyl-6-N-formyl-2',3'-O-isopropylideneadenosine 
• 1174638-91-5 5'-O-benzoyl-6-N-difluoromethyl-2',3'-O-isopropylideneadenosine 

Relevant academic research and scientific papers

Metal-free transesterification catalyzed by tetramethylammonium methyl carbonate

Environmentally benign metal-free tetramethylammonium methyl carbonate is effective as a catalyst for the chemoselective, scalable, and reusable transesterification of various esters and alcohols in common organic solvents. In situ-generated highly active species, tetramethylammonium alkoxides, can greatly avoid self-decomposition at ≤110 °C, and are reusable. In particular, chelating substrates, such as amino alcohols, diols, triols, sugar derivatives, alkaloids, α-amino acid esters, etc., which deactivate conventional metal salt catalysts, can be used. A 100 gram scale biodiesel production was also demonstrated.

Synthesis and structure-activity relationships of adenosine analogs as inhibitors of trypanosomal glyceraldehyde-3-phosphate dehydrogenase. Modifications at positions 5' and 8

A number of 5', N6- and C8, N6-disubstituted adenosine analogs was synthesized and tested for inhibition of trypanosomal glyceraldehyde 3- phosphate dehydrogenase. The most active compound, N6-(3-methyl-2-buteny

Cyclonucleoside Formation and Ring Cleavage in the Reaction of 2',3'-O-Isopropylideneadenosine with Benzoyl Chloride and Its Substituted Derivatives

Reaction conditions suitable for the formation of 8,5'-O-cycloadenosine derivatives in the reaction of 2',3'-O-isopropylideneadenosine (1) with benzoyl chloride and substituted benzoyl chlorides were investigated.Thus, reaction of 1 with p-toluyl chloride