Literature DB >> 11178843

Palladium-catalyzed intramolecular delta-lactam formation of aryl halides and amide-enolates: syntheses of cherylline and latifine.

T Honda1, H Namiki, F Satoh.   

Abstract

[reaction: see text] Palladium-catalyzed intramolecular carbon-carbon bond formation of aryl halides and amide-enolates gave 4-arylisoquinoline derivatives in good yields, which were further converted into the isoquinoline alkaloids cherylline and latifine.

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Year:  2001        PMID： 11178843     DOI： 10.1021/ol0155337

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


  3 in total

1.  Rotational isomers of N-methyl-N-arylacetamides and their derived enolates: implications for asymmetric Hartwig oxindole cyclizations.

Authors:  Jérémie Mandel; Xiaohong Pan; E Ben Hay; Steven J Geib; Craig S Wilcox; Dennis P Curran
Journal:  J Org Chem       Date:  2013-04-09       Impact factor: 4.354

2.  A short synthesis of ±-cherylline dimethyl ether.

Authors:  Bhima Y Kale; Ananta D Shinde; Swapnil S Sonar; Bapurao B Shingate; Sanjeev Kumar; Samir Ghosh; Soodamani Venugopal; Murlidhar S Shingare
Journal:  Beilstein J Org Chem       Date:  2009-12-16       Impact factor: 2.883

3.  Silica-supported polyphosphoric acid in the synthesis of 4-substituted tetrahydroisoquinoline derivatives.

Authors:  Stanimir Manolov; Stoyanka Nikolova; Iliyan Ivanov
Journal:  Molecules       Date:  2013-02-01       Impact factor: 4.411
  3 in total

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