Functionalized main-group organometallics for organic synthesis

Paul Knochel, Eike Hupe, Wolfgang Dohle, David M. Lindsay, Véronique Bonnet, Guy Quéguiner, Andreas Boudier, Felix Kopp, Stéphane Demay, Naka Seidel, M. Isabel Calaza, Viet Anh Vu, Ioannis Sapountzis, Tanasri Bunlaksananusorn

Research output: Contribution to journalArticle

11 Scopus citations

Abstract

Highly functionalized Grignard-reagents can be easily obtained by an iodine-magnesim exchange reaction and further reacted with various electrophiles. Via a B-Zn exchange reaction, a formal Michael addition with umpolung of the reactivity can be achieved. Chiral phosphine ligands can be easily synthesized by a 2.3 sigmatropic rearrangement and used successfully in asymmetric synthesis.

Original languageEnglish (US)
Pages (from-to)11-17
Number of pages7
JournalPure and Applied Chemistry
Volume74
Issue number1
DOIs
StatePublished - Jan 1 2002

ASJC Scopus subject areas

  • Chemistry(all)
  • Chemical Engineering(all)

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    Knochel, P., Hupe, E., Dohle, W., Lindsay, D. M., Bonnet, V., Quéguiner, G., Boudier, A., Kopp, F., Demay, S., Seidel, N., Calaza, M. I., Vu, V. A., Sapountzis, I., & Bunlaksananusorn, T. (2002). Functionalized main-group organometallics for organic synthesis. Pure and Applied Chemistry, 74(1), 11-17. https://doi.org/10.1351/pac200274010011