Literature DB >> 21359298

Synthesis of benzo- and naphtho-fused bicyclo[n.3.1]alkane frameworks with a bridgehead nitrogen function by palladium-catalyzed intramolecular α'-arylation of α-nitroketones.

Giorgio Giorgi1, Swarupananda Maiti, Pilar López-Alvarado, J Carlos Menéndez.   

Abstract

The C-alkylation of cyclic α-nitroketones with α-halobenzyl halides in the presence of DBU followed by a Pd-catalyzed intramolecular C-arylation afforded benzo-and naphtho-fused bicyclo[n.3.1]alkane derivatives (n = 3, 4, 5) in excellent overall yields for the two-step sequence. In some of the reactions starting from α-nitrocyclooctanone, the major products were fused indane derivatives arising from an intramolecular attack of an intermediate Pd species onto the carbonyl group, followed by elimination.

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Year:  2011        PMID: 21359298     DOI: 10.1039/c0ob00526f

Source DB:  PubMed          Journal:  Org Biomol Chem        ISSN: 1477-0520            Impact factor:   3.876


  1 in total

1.  Stereoselective synthesis of tricyclic compounds by intramolecular palladium-catalyzed addition of aryl iodides to carbonyl groups.

Authors:  Jakub Saadi; Christoph Bentz; Kai Redies; Dieter Lentz; Reinhold Zimmer; Hans-Ulrich Reissig
Journal:  Beilstein J Org Chem       Date:  2016-06-16       Impact factor: 2.883

  1 in total

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