Literature DB >> 14583044

Cascade cyclizations and couplings involving nickel enolates.

Gireesh M Mahandru1, Andy R L Skauge, Sanjoy K Chowdhury, Kande K D Amarasinghe, Mary Jane Heeg, John Montgomery.   

Abstract

A new strategy for effecting cascade cyclization processes using nickel enolates has been developed. Nickel enolates may be cleanly generated by the oxidative cyclization of an enal and alkyne with Ni(0), and the resulting enolate may be functionalized by a variety of alkylation processes. Partially and fully intramolecular versions of the process allow the rapid synthesis of complex polycyclics from simple achiral, acyclic precursors.

Entities:  

Year:  2003        PMID: 14583044     DOI: 10.1021/ja037423w

Source DB:  PubMed          Journal:  J Am Chem Soc        ISSN: 0002-7863            Impact factor:   15.419


  2 in total

1.  Chemoselective hydrosilylation of hydroxyketones.

Authors:  Marta L Lage; Scott J Bader; Kanicha Sa-Ei; John Montgomery
Journal:  Tetrahedron       Date:  2013-07-08       Impact factor: 2.457

2.  Nickel-Catalyzed Three-Component Cycloadditions of Enoates, Alkynes, and Aldehydes.

Authors:  Aireal D Jenkins; Michael T Robo; Paul M Zimmerman; John Montgomery
Journal:  J Org Chem       Date:  2020-02-14       Impact factor: 4.354

  2 in total

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