Chemistry of the wittig reaction, IV Simple conversion of aldehydes to 1,1-dichloroalkane and 1,1-dichloro-1-alkene derivatives, useful intermediates for the synthesis of acetylenic compounds

Peter Vinczer, Szilvia Struhar, L. Novák, Csaba Szantay

Research output: Contribution to journalArticle

29 Citations (Scopus)

Abstract

The formation of 1,1-dichloroalkanes and 1,1-dichloro-l-alkenes from aldehyde is described using triphenylphosphine - carbon tetrachloride reagent system. Different products can be formed by changing the reaction conditions.

Original languageEnglish
Pages (from-to)683-686
Number of pages4
JournalTetrahedron Letters
Volume33
Issue number5
DOIs
Publication statusPublished - Jan 28 1992

Fingerprint

Alkynes
Carbon Tetrachloride
Alkenes
Aldehydes
Derivatives
triphenylphosphine

Keywords

  • 1,1-Dichloro-1-alkenes
  • 1,1-Dichloroalkenes
  • Acetylene from Aldehyde
  • Wittig Reaction

ASJC Scopus subject areas

  • Biochemistry
  • Organic Chemistry
  • Drug Discovery

Cite this

Chemistry of the wittig reaction, IV Simple conversion of aldehydes to 1,1-dichloroalkane and 1,1-dichloro-1-alkene derivatives, useful intermediates for the synthesis of acetylenic compounds. / Vinczer, Peter; Struhar, Szilvia; Novák, L.; Szantay, Csaba.

In: Tetrahedron Letters, Vol. 33, No. 5, 28.01.1992, p. 683-686.

Research output: Contribution to journalArticle

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AU - Szantay, Csaba

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