77655-45-9Relevant academic research and scientific papers
An efficient one-pot, three-component reaction: Synthesis of complex-annelated α-carbolines via an intramolecular [3+2]-dipolar cycloaddition reaction
Majumder, Swarup,Bhuyan, Pulak J.
experimental part, p. 1547 - 1550 (2011/08/04)
Novel annelated α-carbolines have been synthesized from oxindole using three components in a one-pot procedure involving an intramolecular [3+2]-dipolar cycloaddition reaction of azides to nitriles. Georg Thieme Verlag Stuttgart ? New York.
Photoinduced intramolecular addition of 3-acyl-2-haloindoles to alkenes
Lu, Shen-Ci,Duan, Xiao-Yong,Shi, Zong-Jun,Li, Bing,Ren, Yu-Wei,Zhang, Wei,Zhang, Yong-Hui,Tu, Zhi-Feng
supporting information; experimental part, p. 3902 - 3905 (2009/12/03)
1,2-Fused indoles and pyrroles were prepared via an efficient intmolecular photoaddition reaction of 1-(ωalkenyl)-2 haloindole-3-carbaldehydes and 1-(ωalkenyl)-2 chloropyrrole-3-carbaldehydes. The presence of an acyl group was necessary for the photocycizntion reactions. The halogen-atom retained exo and endo cyclization prodects were generally prodeced with result similar to those of atom transfer cyclization reaction. in contrast, unsaturated cyclization prodects were obtained in the photoreactions of substrates having monthyl groups on vinyl group.
