New routes to 1,1-dichloro-4-methyl-1,3-pentadiene

István Bitter, László T ' ́oke, Zoltán Bende, Éva Kárpáti-Ádám, Rudolf Soós

Research output: Contribution to journalArticle

2 Citations (Scopus)

Abstract

l,l,l-trichloro-2-hydroxy-4-methyl-pentene-3 (lb) was chlorinated to afford tri- and tetra-chlorinated compounds 2,3,4 Compounds 2 and 3_ were transformed by reductive dechlorination into l,l.-dichloro-4-methyl-1,3-pentadiene (2b). Another route starting from the same alcohol or its isomer was also developed.

Original languageEnglish
Pages (from-to)4501-4505
Number of pages5
JournalTetrahedron
Volume40
Issue number21
DOIs
Publication statusPublished - 1984

ASJC Scopus subject areas

  • Biochemistry
  • Drug Discovery
  • Organic Chemistry

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  • Cite this

    Bitter, I., T ' ́oke, L., Bende, Z., Kárpáti-Ádám, É., & Soós, R. (1984). New routes to 1,1-dichloro-4-methyl-1,3-pentadiene. Tetrahedron, 40(21), 4501-4505. https://doi.org/10.1016/S0040-4020(01)98826-X