Literature DB >> 28742365

Divergent Synthesis of Polycyclic Indolines: Copper-Catalyzed Cascade Reactions of Propargylic Carbamates and Indoles.

Tian-Ren Li1, Liang-Qiu Lu1, Ya-Ni Wang1, Bao-Cheng Wang1, Wen-Jing Xiao1,2.   

Abstract

Polycyclic indolines are the common and core structural motif of many indole alkaloids that usually exhibit biological activities. Here, we describe two copper-catalyzed cascade reactions between propargylic carbamates and indoles. By doing so, one-step and divergent synthesis of structurally distinct polycyclic indolines, quinoline-fused indolines, C(3a)-indolyl furoindolines, and pyrroloindolines was achieved in high synthetic efficiency and selectivity.

Entities:  

Year:  2017        PMID: 28742365     DOI: 10.1021/acs.orglett.7b01903

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  2 in total

1.  Two Catalytic Annulation Modes via Cu-Allenylidenes with Sulfur Ylides that Are Dominated by the Presence or Absence of Trifluoromethyl Substituents.

Authors:  Malla Reddy Gannarapu; Jun Zhou; Bingyao Jiang; Norio Shibata
Journal:  iScience       Date:  2020-03-20

2.  Electrooxidation enables highly regioselective dearomative annulation of indole and benzofuran derivatives.

Authors:  Kun Liu; Wenxu Song; Yuqi Deng; Huiyue Yang; Chunlan Song; Takfaoui Abdelilah; Shengchun Wang; Hengjiang Cong; Shan Tang; Aiwen Lei
Journal:  Nat Commun       Date:  2020-01-07       Impact factor: 14.919

  2 in total

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