Literature DB >> 22228267

Copper-catalyzed domino intramolecular cyclization: a facile and efficient approach to polycyclic indole derivatives.

Ziming Xia1, Kuo Wang, Jiening Zheng, Zheyong Ma, Zhanguo Jiang, Xiaoxia Wang, Xin Lv.   

Abstract

A mild and efficient Cu(2)O-catalyzed domino intramolecular C-N coupling/C-Y (Y = O, S, N) bond formation was successfully achieved. Thus oxazino[3,2-a]indole, thiazino[3,2-a]indole and indolo[2,1-b]quinazoline derivatives were facilely assembled from readily accessible gem-dibromovinyl systems. The protocol is general and practical, affording a variety of the indole-incorporated products in good to excellent yields even under air atmosphere.

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Year:  2012        PMID: 22228267     DOI: 10.1039/c1ob06488f

Source DB:  PubMed          Journal:  Org Biomol Chem        ISSN: 1477-0520            Impact factor:   3.876


  1 in total

1.  Elucidating the mechanism and origins of selectivity on catalyst-dependent cyclization reactions to form polycyclic indolines from a theoretical study.

Authors:  Yan Zhang; Yongsheng Yang; Ying Xue
Journal:  RSC Adv       Date:  2021-06-09       Impact factor: 4.036

  1 in total

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