Literature DB >> 31829606

Preparation of 4-Diazoisoquinolin-3-ones via Dimroth Rearrangement and Their Extension to 4-Aryltetrahydroisoquinolin-3-ones.

Zhenmin Li1, Junrong Chen1, Li Wu1, Anni Ren1, Ping Lu1, Yanguang Wang1.   

Abstract

4-Diazoisoquinolin-3-ones were prepared efficiently via TBAB-promoted rearrangement of 4-diazoisochroman-3-imines under mild reaction conditions. The resulted 4-diazoisoquinolin-3-ones could be conveniently applied for the synthesis of 4-aryltetrahydroisoquinolin-3-ones either by the TfOH-catalyzed reaction with electron-rich arenes or by the BF3-promoted reaction with aryl aldehydes.

Entities:  

Year:  2019        PMID: 31829606     DOI: 10.1021/acs.orglett.9b03708

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


  3 in total

1.  The Dimroth Rearrangement in the Synthesis of Condensed Pyrimidines - Structural Analogs of Antiviral Compounds.

Authors:  Vakhid А Mamedov; Nataliya А Zhukova; Milyausha S Kadyrova
Journal:  Chem Heterocycl Compd (N Y)       Date:  2021-05-15       Impact factor: 1.277

2.  Facile and diastereoselective arylation of the privileged 1,4-dihydroisoquinolin-3(2H)-one scaffold.

Authors:  Dmitry Dar'in; Grigory Kantin; Alexander Bunev; Mikhail Krasavin
Journal:  Beilstein J Org Chem       Date:  2022-08-22       Impact factor: 2.544

3.  Metal-free tandem carbene N-H insertions and C-C bond cleavages.

Authors:  Pu Chen; Jiang Nan; Yan Hu; Yifan Kang; Bo Wang; Yangmin Ma; Michal Szostak
Journal:  Chem Sci       Date:  2020-11-10       Impact factor: 9.825

  3 in total

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