486420-76-2

Upstream product

• 128084-00-4 (+/-)-7β,8α,9α-tris(benzoyloxy)-10β-amino-7,8,9,10-tetrahydrobenzopyrene 
• 135560-86-0 6-fluoro-9-(2-deoxy-3,5-bis-O-(tert-butyldimethylsilyl)-β-D-erytropentofuranosyl)purine 
• 106568-82-5 6-chloro-9-[2'-deoxy-3',5'-bis-O-(tert-butyldimethylsilyl)-β-D-erythropentofuranosyl]purine 
• 228704-85-6 6-bromo-9-(2-deoxy-3,5-bis-O-(tert-butyldimethylsilyl)-β-D-erythro-pentofuranosyl)purine 
• 57405-08-0 (+/-)-trans-7,8-Dihydrobenzopyrene-7,8-diol dibenzoate 

Relevant academic research and scientific papers

Palladium-catalyzed synthesis of nucleoside adducts from bay- and fjord-region diol epoxides

(Chemical Equation Presented) Palladium-catalyzed C-N bond formation has been utilized to synthesize covalent 2′-deoxyadenosine (dA) and 2′-deoxyguanosine (dG) adducts of benzo[a]pyrene (BaP) series 1 (syn) and benzo[c]phenanthrene (BcPh) series 2 (anti)

Palladium-catalyzed synthesis of carcinogenic polycyclic aromatic hydrocarbon epoxide-nucleoside adducts: The first amination of a chloro nucleoside

(Matrix presented) Pd-catalyzed coupling of the axially constrained, less reactive benzo[a]pyrene bay-region amino benzoates, derived from the tetrahydro and diol epoxides, with C-6 and C-2 halopurine deoxynucleosides offers an efficient approach to the s