Regio-controlled radical substitution of 9-substituted purines
摘要:
9-benzylpurine undergoes facile radical alkylation and acylation under standard Minisci's conditions affording regioselectively 6-substituted derivatives.
Dihydroxylation of 6-vinylpurines with t-BuOOH and OSO4 gave 6-(1,2-dihydroxyethyl)purines 2, while the epoxidation with H2WO4 and t-BuOOH afforded 6-(oxiran-2-yl)purines 3. Oxirane ring-opening reactions of 3 with diverse nucleophiles gave a series of title 6-(1,2-disubstituted ethyl)purine bases and nucleosides, which were tested for cytostatic and antiviral activities. (C) 2008 Published by Elsevier Ltd.
Gundersen Lise-Lotte, Bakkestuen Anne Kristin, Aasen Arne Jorgen, Overas +, Tetrahedron, 50 (1994) N 32, S 9743-9756
作者:Gundersen Lise-Lotte, Bakkestuen Anne Kristin, Aasen Arne Jorgen, Overas +
DOI:——
日期:——
6-Halopurines in palladium-catalyzed coupling with organotin and organozinc reagents
N-9 and N-7 benzylated 6-halopurines readily participate in palladium catalyzed cross coupling reactions with organotin and organozinc derivati
N -9和N -7苄基化的6-卤尿烷易于参与钯催化的有机锡和有机锌衍生物的交叉偶联反应
Regio-controlled radical substitution of 9-substituted purines
作者:Laurent Désaubry、Jean-Jacques Bourguignon
DOI:10.1016/0040-4039(95)01647-z
日期:1995.10
9-benzylpurine undergoes facile radical alkylation and acylation under standard Minisci's conditions affording regioselectively 6-substituted derivatives.