80699-32-7Relevant articles and documents
The Suzuki-Miyaura cross-coupling reactions of 2-, 6- or 8-halopurines with boronic acids leading to 2-, 6- or 8-aryl- and -alkenylpurine derivatives
Havelkova,Dvorak,Hocek
, p. 1704 - 1710 (2001)
The Suzuki-Miyaura cross-coupling reactions of 9-benzyl-6-chloropurine, 9- or 3-benzyl-8-bromoadenine and 2,6-dihalopurines with boronic acids gave the corresponding 6-, 8- or 2-aryl- or -alkenylpurines in good yields. Anhydrous conditions in toluene were
NMR and X-ray structural studies on 3-benzyl-8-bromoadenine
Siah, Huey-San Melanie,Goerbitz, Carl Henrik,Gundersen, Lise-Lotte
experimental part, p. 1375 - 1378 (2012/01/12)
8-Bromoadenine was benzylated in the presence of base to give a mixture of two regioisomers. One was easily recognized as 9-benzyl-8-bromoadenine, but the other structure could not be determined with absolute certainty by NMR. Therefore, X-ray crystallogr