Literature DB >> 28920700

Highly Selective Construction of Medium-Sized Lactams by Palladium-Catalyzed Intramolecular Hydroaminocarbonylation of Aminoalkynes.

Yue Hu1,2, Hanmin Huang1,3.   

Abstract

A novel palladium-catalyzed intramolecular hydroaminocarbonylation of aminoalkynes has been developed. This direct and operationally simple protocol provides a rapid and reliable approach to a diverse array of valuable seven- and eight-membered lactams with high chemoselectivity and regioselectivity. The high selectivity might be attributed to rational tuning the electronic nature of the amine moiety and the palladium catalyst, which enabled this transformation to proceed in the absence of acidic or any other additives under fairly mild reaction conditions. This method paves the way for the synthesis of medium-sized lactams.

Entities:  

Year:  2017        PMID: 28920700     DOI: 10.1021/acs.orglett.7b02284

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


  1 in total

1.  Modular Access to Azepines by Directed Carbonylative C-C Bond Activation of Aminocyclopropanes.

Authors:  Gang-Wei Wang; John F Bower
Journal:  J Am Chem Soc       Date:  2018-02-20       Impact factor: 15.419

  1 in total

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