Literature DB >> 17305348

Benzylic substitution of gramines with boronic acids and rhodium or iridium catalysts.

Gabriela de la Herran1, Amaya Segura, Aurelio G Csákÿ.   

Abstract

Gramine-MeI salts were useful starting materials for the synthesis of 3-benzyl- and 3-allylindoles by the 1,4-addition of boronic acids to the C=C-C=N linkages generated in situ under Rh(I)-catalysis. On the other hand, under Ir(I) catalysis, the reaction of gramines with indoles was used to produce nonsymmetrical diindolylmethanes. [reaction: see text]

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Year:  2007        PMID: 17305348     DOI: 10.1021/ol063042m

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


  4 in total

1.  Asymmetric synthesis via stereospecific C-N and C-O bond activation of alkyl amine and alcohol derivatives.

Authors:  Sarah M Pound; Mary P Watson
Journal:  Chem Commun (Camb)       Date:  2018-10-30       Impact factor: 6.222

2.  Nickel-catalyzed cross couplings of benzylic ammonium salts and boronic acids: stereospecific formation of diarylethanes via C-N bond activation.

Authors:  Prantik Maity; Danielle M Shacklady-McAtee; Glenn P A Yap; Eric R Sirianni; Mary P Watson
Journal:  J Am Chem Soc       Date:  2012-12-26       Impact factor: 15.419

Review 3.  Synthesis and stereochemical determination of an antiparasitic pseudo-aminal type monoterpene indole alkaloid.

Authors:  Yoshihiko Noguchi; Tomoyasu Hirose; Aki Ishiyama; Masato Iwatsuki; Kazuhiko Otoguro; Toshiaki Sunazuka; Satoshi Ōmura
Journal:  J Nat Med       Date:  2016-06-21       Impact factor: 2.343

Review 4.  C4-H indole functionalisation: precedent and prospects.

Authors:  Jagadeesh Kalepu; Parthasarathy Gandeepan; Lutz Ackermann; Lukasz T Pilarski
Journal:  Chem Sci       Date:  2018-04-20       Impact factor: 9.825

  4 in total

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