38930-69-7

Upstream product

• 43077-06-1 6-N-benzoyl-2',3'-O-isopropylideneadenosine-5'-aldehyde 
• 1779-49-3 Methyltriphenylphosphonium bromide 
• 39947-04-1 N-6-benzoyl-2',3'-O-isopropylideneadenosine 
• 43077-04-9 6-N-benzoyl-9-(2,3-O-isopropylidene-β-D-ribo-pentodialdo-1,5-furanosyl)adeninehydrate 
• 43077-03-8 N⁶-benzoyl-5'-deoxy-2',3'-O-isopropylidiene-5',5'-(N,N'-diphenylethylenediamino)adenosine 
• 245544-64-3 2',3'-O-isopropylidene-5'-O-(trimethylsilyl)adenosine 
• 362-75-4 2',3'-isopropylidene adenosine 

Downstream Products

• 163668-04-0 N-{9-[(3aR,4R,6S,6aS)-6-(1-Bromo-vinyl)-2,2-dimethyl-tetrahydro-furo[3,4-d][1,3]dioxol-4-yl]-9H-purin-6-yl}-benzamide 

Relevant academic research and scientific papers

Hemisynthesis of deuteriated adenosylhopane and conversion into bacteriohopanetetrol by a cell-free system from Methylobacterium organophilum

Adenosylhopane is a putative precursor of the widespread bacterial C35 biohopanoids. A concise and flexible hemisynthesis of adenosylhopane has been developed including as key steps a cross metathesis between two olefins containing either the h

Nucleic acid related compounds. 84. Synthesis of 6'-(E and Z)- halohomovinyl derivatives of adenosine, inactivation of S-adenosyl-L- homocysteine hydrolase, and correlation of anticancer and antiviral potencies with enzyme inhibition

Treatment of 9-[6-(E)-(tributylstannyl)-5,6-dideoxy-2,3-O-isopropylidene- β-D-ribo-hex-5-enofuranosyl]adenine [2b(E)] or the 6-N-benzoyl derivative 2a(E) with iodine (or N-iodosuccinimide) or bromine (or N-bromosuccinimide) gave virtually quantitative and