Synthesis of indoles via alkylidenation of acyl hydrazides

Hisler, K. and Commeureuc, A.G.J. and Zhou, S.Z. and Murphy, J.A., EPSRC (Funder), WestCHEM (Funder) (2009) Synthesis of indoles via alkylidenation of acyl hydrazides. Tetrahedron Letters, 50 (26). pp. 3290-3293. ISSN 0040-4039 (https://doi.org/10.1016/j.tetlet.2009.02.060)

Preview

PDF. Filename: science.pdf Final Published Version Download (506kB)| Preview

Abstract

Indoles have been synthesised via alkylidenation of acyl phenylhydrazides using phosphoranes and the Petasis reagent, followed by in situ thermal rearrangement of the product enehydrazines. The Petasis reagent provides an essentially neutral equivalent of the [acid-catalysed] Fischer indole synthesis, but with acyl phenylhydrazides as starting substrates. Alkylidene triphenylphosphoranes convert aroyl phenylhydrazides to indoles, but acyl phenylhydrazides derived from aliphatic carboxylic acids undergo a Brunner reaction to form indolin-2-ones.

• Share and Export
  

  RDF+XMLBibTeXRIOXX2 XMLRDF+N-TriplesJSONDublin CoreAtomSimple MetadataReferMETSHTML CitationASCII CitationOpenURL ContextObjectEndNoteOpenURL ContextObject in SpanMODSMPEG-21 DIDLEP3 XMLData Cite XMLRIS (EndNote Online, Zotero, Ref manager, etc)RDF+N3Multiline CSV
• Item metadata

  Item type:	Article
  ID code:	19092
  Dates:	Date Event 1 July 2009 Published
  Subjects:	Science > Chemistry
  Department:	Faculty of Science > Pure and Applied Chemistry
  Depositing user:	Strathprints Administrator
  Date deposited:	15 Jun 2010 09:19
  Last modified:	11 Nov 2024 09:26
  URI:	https://strathprints.strath.ac.uk/id/eprint/19092