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Amarender Manchoju Renaud Zelli Gang Wang Carla Eymard Adrian Oo Mona Nemer Michel Prvost Baek Kim Yvan Guindon 《Molecules (Basel, Switzerland)》2022,27(2)
The design of novel nucleoside triphosphate (NTP) analogues bearing an all-carbon quaternary center at C2′ or C3′ is described. The construction of this all-carbon stereogenic center involves the use of an intramoleculer photoredox-catalyzed reaction. The nucleoside analogues (NA) hydroxyl functional group at C2′ was generated by diastereoselective epoxidation. In addition, highly enantioselective and diastereoselective Mukaiyama aldol reactions, diastereoselective N-glycosylations and regioselective triphosphorylation reactions were employed to synthesize the novel NTPs. Two of these compounds are inhibitors of the RNA-dependent RNA polymerase (RdRp) of SARS-CoV-2, the causal virus of COVID-19. 相似文献
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Batchu VR Barange DK Kumar D Sreekanth BR Vyas K Reddy EA Pal M 《Chemical communications (Cambridge, England)》2007,(19):1966-1968
A new one-pot reaction for the regioselective construction of a six-membered fused N-heterocyclic ring leading to isoquinolones under Pd/C-Cu catalysis is described. 相似文献
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