Synthesis of Pyrrolo[2,3-b]indole via Iodine(III)-Mediated Intramolecular Annulation
Tu, Dandan1,2; Ma, Liying1; Tong, Xiaogang1,2; Deng, Xu1; Xia, Chengfeng1
2012-09-21
Source PublicationORGANIC LETTERS
Volume14Issue:18Pages:4830-4833
AbstractNew synthetic procedures for the pyrrolo[2,3-b]indole skeleton have been developed via intramolecular annulation of indole derivatives under iodine(III). A series of indole derivatives with different protecting groups or substitutions were explored to facilitate the corresponding pyrrolo[2,3-b]indole compounds in excellent yields.
DOI10.1021/ol302158h
Indexed BySCI ; IC ; CCR
Language英语
WOS Research AreaChemistry
WOS SubjectChemistry, Organic
WOS IDWOS:000308958500033
Citation statistics
Document Type期刊论文
Identifierhttp://ir.kib.ac.cn/handle/151853/20432
Collection植物化学与西部植物资源持续利用国家重点实验室
Affiliation1.Chinese Acad Sci, Kunming Inst Bot, State Key Lab Phytochem & Plant Resources W China, Kunming 650201, Peoples R China
2.Chinese Acad Sci, Grad Univ, Beijing 100049, Peoples R China
Recommended Citation
GB/T 7714
Tu, Dandan,Ma, Liying,Tong, Xiaogang,et al. Synthesis of Pyrrolo[2,3-b]indole via Iodine(III)-Mediated Intramolecular Annulation[J]. ORGANIC LETTERS,2012,14(18):4830-4833.
APA Tu, Dandan,Ma, Liying,Tong, Xiaogang,Deng, Xu,&Xia, Chengfeng.(2012).Synthesis of Pyrrolo[2,3-b]indole via Iodine(III)-Mediated Intramolecular Annulation.ORGANIC LETTERS,14(18),4830-4833.
MLA Tu, Dandan,et al."Synthesis of Pyrrolo[2,3-b]indole via Iodine(III)-Mediated Intramolecular Annulation".ORGANIC LETTERS 14.18(2012):4830-4833.
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