Literature DB >> 10990431

Palladium(II)-catalyzed tandem intramolecular aminopalladation of alkynes and conjugate addition. Synthesis of oxazolidinones, imidazolidinones, and lactams

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Abstract

[reaction: see text]Under the catalysis of a divalent palladium species, oxazolidinones, imidazolidinones, or lactams were conveniently obtained with high chemo- and stereoselectivity from the tandem intramolecular aminopalladation of alkynes, followed by insertion of alkenes, and protonolysis of the newly formed carbon-palladium bond.

Entities:  

Year:  2000        PMID: 10990431     DOI: 10.1021/ol006266s

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


  2 in total

1.  Stereoselective synthesis of imidazolidin-2-ones via Pd-catalyzed alkene carboamination. Scope and limitations.

Authors:  Jonathan A Fritz; John P Wolfe
Journal:  Tetrahedron       Date:  2008       Impact factor: 2.457

2.  N-Amino-imidazolin-2-one peptide mimic synthesis and conformational analysis.

Authors:  Caroline Proulx; William D Lubell
Journal:  Org Lett       Date:  2012-08-14       Impact factor: 6.005

  2 in total

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