Literature DB >> 27128964

Divergent Syntheses of Carbazole Alkaloids Clausenapin, Indizoline, Claulansine M, and Clausenaline D.

Yizhen Liu1, Yanqin Guo1, Feixiang Ji1, Dong Gao1, Chuanjun Song1, Junbiao Chang1.   

Abstract

We described the first total syntheses of clausenapin, indizoline, claulansine M, and a novel synthetic route to clausenaline D via divergent method. Key steps involved TFAA-mediated intramolecular acylation to construct the carbazole core and subsequent Claisen rearrangement to generate key intermediates for further elaboration to target molecules.

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Year:  2016        PMID: 27128964     DOI: 10.1021/acs.joc.6b00729

Source DB:  PubMed          Journal:  J Org Chem        ISSN: 0022-3263            Impact factor:   4.354


  2 in total

1.  A Rh(II)-catalyzed highly stereoselective [3 + 2] annulation of vinyl diazoacetates with indole-2-carbaldehyde for the synthesis of indolyl dihydrofurans.

Authors:  Rimei Zheng; Aimin Xu; Jiawu Huang; Zhijing Zhang; Xinru Yin; Tianyuan Zhang; Wenhao Hu; Yu Qian
Journal:  Mol Divers       Date:  2022-01-20       Impact factor: 2.943

2.  Rh(III)-Catalyzed C-H Activation/Intramolecular Cyclization: Access to N-Acyl-2,3-dihydro-1H-carbazol-4(9H)-ones from Cyclic 2-Diazo-1,3-diketones and N-Arylamides.

Authors:  Youpeng Zuo; Xinwei He; Yi Ning; Yuhao Wu; Yongjia Shang
Journal:  ACS Omega       Date:  2017-11-30
  2 in total

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