Our official English website, www.x-mol.net, welcomes your
feedback! (Note: you will need to create a separate account there.)
Rh(II)-Catalyzed Condensations of N-Sulfonyl-1,2,3-triazoles with Aminals
SynOpen ( IF 2.0 ) Pub Date : 2021-04-13 , DOI: 10.1055/a-1480-8884 Nidal Saleh 1 , Jerome Lacour 1
SynOpen ( IF 2.0 ) Pub Date : 2021-04-13 , DOI: 10.1055/a-1480-8884 Nidal Saleh 1 , Jerome Lacour 1
Affiliation
N-Sulfonyl-1,2,3-triazoles react with cyclic N,N’-diaryl aminals under dirhodium catalysis to generate, after ylide formation and subsequent ring opening, original imino-iminium intermediates. Quite a few recent synthetic applications have been reported using these electrophilic moieties, in particular series of cascade reactions forming unprecedented polycyclic polyaza derivatives.
中文翻译:
Rh(II)催化N-磺酰基-1,2,3-三唑与缩醛的缩合反应
N-磺酰基-1,2,3-三唑类化合物在环状碘催化下与环状N,N'-二芳基缩醛反应生成内酯并随后开环后,生成原始的亚氨基-亚胺基中间体。使用这些亲电子部分,特别是一系列级联反应,形成了前所未有的多环多氮杂衍生物,已经报道了许多最近的合成应用。
更新日期:2021-05-22
中文翻译:
Rh(II)催化N-磺酰基-1,2,3-三唑与缩醛的缩合反应
N-磺酰基-1,2,3-三唑类化合物在环状碘催化下与环状N,N'-二芳基缩醛反应生成内酯并随后开环后,生成原始的亚氨基-亚胺基中间体。使用这些亲电子部分,特别是一系列级联反应,形成了前所未有的多环多氮杂衍生物,已经报道了许多最近的合成应用。