Literature DB >> 26902777

Opening the Way to Catalytic Aminopalladation/Proxicyclic Dehydropalladation: Access to Methylidene γ-Lactams.

Mélanie M Lorion1, Filipe J S Duarte2, Maria José Calhorda2, Julie Oble1, Giovanni Poli1.   

Abstract

A new aerobic intramolecular palladium(II)-based catalytic system that triggers aminopalladation/dehydropalladation of N-sulfonylalkenylamides to give the corresponding methylidene γ-lactams has been identified. Use of triphenylphosphine and chloride anion as ligands is mandatory for optimal yields, and molecular oxygen can be used as the sole terminal oxidant. Scope and limitations of the methods are described. A mechanism is proposed on the basis of experimental results as well as density functional theory calculations.

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Year:  2016        PMID: 26902777     DOI: 10.1021/acs.orglett.6b00143

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


  1 in total

1.  Switchable selectivity in Pd-catalyzed [3 + 2] annulations of γ-oxy-2-cycloalkenones with 3-oxoglutarates: C-C/C-C vs C-C/O-C bond formation.

Authors:  Yang Liu; Julie Oble; Giovanni Poli
Journal:  Beilstein J Org Chem       Date:  2019-05-16       Impact factor: 2.883

  1 in total

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