Palladium catalysed alkylative dimerization between pronucleophiles and vinyltins

Itaru Nakamura, Naofumi Tsukada, Mohammad Al-Masum, Yoshinori Yamamoto

Research output: Contribution to journalArticlepeer-review

3 Citations (Scopus)


In the presence of catalytic amounts of Pd2(dba)3·CHCl3 and dppb, the reaction of pronucleophiles 1 with vinyltins 2 gives the corresponding alkylative dimerization products of the vinyl group, 1,4-disubstituted butene derivatives 3, in good to high yields.

Original languageEnglish
Pages (from-to)1583-1584
Number of pages2
JournalChemical Communications
Issue number16
Publication statusPublished - 1997 Jan 1
Externally publishedYes

ASJC Scopus subject areas

  • Catalysis
  • Electronic, Optical and Magnetic Materials
  • Ceramics and Composites
  • Chemistry(all)
  • Surfaces, Coatings and Films
  • Metals and Alloys
  • Materials Chemistry


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