Literature DB >> 25872155

Direct access to functionalized benzotropones, azepanes, and piperidines by reductive cross-coupling of α-bromo enones with α-bromo enamides.

Timothy K Beng1, Kayla Sincavage, Ann Wens V Silaire, Amir Alwali, Daniel P Bassler, Laura E Spence, Oliver Beale.   

Abstract

The synthesis of functionalized azepenes and piperidines bearing an α-cycloheptenone or benzotropone derivative has been accomplished through direct reductive cross-coupling of α-bromo eneformamides or enecarbamates with highly versatile α-bromo benzotropone derivatives, under cobalt catalysis. The coupling products have been further elaborated to other synthetically useful aza-heterocyclic frameworks.

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Year:  2015        PMID: 25872155     DOI: 10.1039/c5ob00517e

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


  2 in total

1.  Multimetallic Ni- and Pd-Catalyzed Cross-Electrophile Coupling To Form Highly Substituted 1,3-Dienes.

Authors:  Astrid M Olivares; Daniel J Weix
Journal:  J Am Chem Soc       Date:  2018-02-08       Impact factor: 15.419

Review 2.  One hundred years of benzotropone chemistry.

Authors:  Arif Dastan; Haydar Kilic; Nurullah Saracoglu
Journal:  Beilstein J Org Chem       Date:  2018-05-23       Impact factor: 2.883

  2 in total

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