Literature DB >> 17559273

A general modular method of azaindole and thienopyrrole synthesis via Pd-catalyzed tandem couplings of gem-dichloroolefins.

Yuan-Qing Fang1, Josephine Yuen, Mark Lautens.   

Abstract

A palladium-catalyzed reaction of gem-dichloroolefins and a boronic acid via a tandem intramolecular C-N and intermolecular Suzuki coupling process gave corresponding substituted azaindoles or thienopyrroles. This method is a very modular protocol to synthesize all four isomers of azaindole and two isomers of thienopyrroles in good to excellent yield.

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Year:  2007        PMID: 17559273     DOI: 10.1021/jo070460b

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


  4 in total

1.  Towards rational design of cannabinoid receptor 1 (CB1) antagonists for peripheral selectivity.

Authors:  Alan Fulp; Katherine Bortoff; Yanan Zhang; Herbert Seltzman; Rodney Snyder; Rangan Maitra
Journal:  Bioorg Med Chem Lett       Date:  2011-08-11       Impact factor: 2.823

Review 2.  Biaryl phosphane ligands in palladium-catalyzed amination.

Authors:  David S Surry; Stephen L Buchwald
Journal:  Angew Chem Int Ed Engl       Date:  2008       Impact factor: 15.336

3.  Synthesis of a 7-azaindole by chichibabin cyclization: reversible base-mediated dimerization of 3-picolines.

Authors:  Yun Ma; Sean Breslin; Ivan Keresztes; Emil Lobkovsky; David B Collum
Journal:  J Org Chem       Date:  2008-12-19       Impact factor: 4.354

Review 4.  Metal-Catalyzed Cross-Coupling Reactions on Azaindole Synthesis and Functionalization.

Authors:  A Sofia Santos; Ana C Mortinho; M Manuel B Marques
Journal:  Molecules       Date:  2018-10-17       Impact factor: 4.411

  4 in total

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