Literature DB >> 24833410

Palladium-catalyzed α-ketocyclopropanation of norbornenes with propargyl acetates.

Yuta Tanioka1, Naofumi Tsukada.   

Abstract

Propargyl acetates reacted with norbornene in the presence of a catalytic amount of tetrakis(tripheylphosphine)palladium to give cyclopropyl ketones. The reaction proceeded with high stereoselectivity, affording a single stereoisomer. The reaction of various substituted norbornenes gave the corresponding cyclopropanes in moderate to good yields.

Entities:  

Year:  2014        PMID: 24833410     DOI: 10.1021/jo500357f

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


  1 in total

1.  Sequential Insertion of Alkynes, Alkenes, and CO into the Pd-C Bond of ortho-Palladated Primary Phenethylamines: from η3-Allyl Complexes and Enlarged Palladacycles to Functionalized Arylalkylamines.

Authors:  José-Antonio García-López; María-José Oliva-Madrid; Delia Bautista; José Vicente; Isabel Saura-Llamas
Journal:  Organometallics       Date:  2021-01-29       Impact factor: 3.876

  1 in total

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