Literature DB >> 17134268

Rearrangement of 3,3-disubstituted indolenines and synthesis of 2,3-substituted indoles.

Kevin G Liu1, Albert J Robichaud, Jennifer R Lo, James F Mattes, Yanxuan Cai.   

Abstract

Synthesis of 2,3-substituted indoles from phenylhydrazine and alpha-branched aldehydes via rearrangement of 3,3-disubstituted indolenine intermediates is reported. [reaction: see text]

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Year:  2006        PMID： 17134268     DOI： 10.1021/ol0623567

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


  3 in total

1.  Fe(II)-catalyzed amination of aromatic C-H bonds via ring opening of 2H-azirines: synthesis of 2,3-disubstituted indoles.

Authors:  Samaresh Jana; Mack D Clements; Barry K Sharp; Nan Zheng
Journal:  Org Lett       Date:  2010-09-03       Impact factor: 6.005

2.  Unified biogenesis of ambiguine, fischerindole, hapalindole and welwitindolinone: identification of a monogeranylated indolenine as a cryptic common biosynthetic intermediate by an unusual magnesium-dependent aromatic prenyltransferase.

Authors:  Xinyu Liu; Matthew L Hillwig; Leonardus M I Koharudin; Angela M Gronenborn
Journal:  Chem Commun (Camb)       Date:  2016-01-07       Impact factor: 6.222

3.  Total Synthesis of (±)-Exotine B.

Authors:  Bichu Cheng; Giulio Volpin; Johannes Morstein; Dirk Trauner
Journal:  Org Lett       Date:  2018-07-06       Impact factor: 6.005
  3 in total

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