Literature DB >> 12357784

A novel scandium ortho-methoxynitrosobenzene-dimer complex: mechanistic implications for the nitroso-Diels-Alder reaction.

Andrew P Lightfoot1, Robin G Pritchard, Hayley Wan, John E Warren, Andrew Whiting.   

Abstract

Arylnitroso dienophiles exist in equilibrium with their dimeric counterparts, which in turn form stable bidentate complexes with scandium(III) triflate and react with cyclohexadiene to give the corresponding Diels-Alder adduct at the same rate as the normal thermal process.

Entities:  

Year:  2002        PMID: 12357784     DOI: 10.1039/b206366b

Source DB:  PubMed          Journal:  Chem Commun (Camb)        ISSN: 1359-7345            Impact factor:   6.222


  2 in total

1.  Catalytic asymmetric nitroso-Diels-Alder reaction with acyclic dienes.

Authors:  Yuhei Yamamoto; Hisashi Yamamoto
Journal:  Angew Chem Int Ed Engl       Date:  2005-11-04       Impact factor: 15.336

Review 2.  The nitrosocarbonyl hetero-Diels-Alder reaction as a useful tool for organic syntheses.

Authors:  Brian S Bodnar; Marvin J Miller
Journal:  Angew Chem Int Ed Engl       Date:  2011-04-21       Impact factor: 15.336

  2 in total

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