Literature DB >> 16220938

A new catalytic conjugate addition/aldol strategy that avoids preformed metalated nucleophiles.

Kandasamy Subburaj1, John Montgomery.   

Abstract

A new conjugate addition/aldol strategy has been developed. Unlike conventional procedures that require metalation of the nucleophilic species, the procedure allows the direct coupling of aryl iodides, aldehydes, and acrylates in a nickel-catalyzed, organozinc-promoted process.

Entities:  

Year:  2003        PMID： 16220938     DOI： 10.1021/ja0362048

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


  3 in total

1.  Direct Copper-Free Domino Conjugate Addition-Cycloallylation using Organozinc Reagents.

Authors:  Venukrishnan Komanduri; Fernando Pedraza; Michael J Krische
Journal:  Adv Synth Catal       Date:  2008-07-07       Impact factor: 5.837

2.  Nickel-catalyzed reductive conjugate addition to enones via allylnickel intermediates.

Authors:  Ruja Shrestha; Stephanie C M Dorn; Daniel J Weix
Journal:  J Am Chem Soc       Date:  2013-01-08       Impact factor: 15.419

3.  Nickel-Catalyzed Annulations of ortho-Haloarylimines.

Authors:  Srinivas Kolluru; Manvendra Singh; Bryce Gaskins; Zarko Boskovic
Journal:  ACS Catal       Date:  2021-08-05       Impact factor: 13.700
  3 in total

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