Synthesis 2002(14): 1987-1992
DOI: 10.1055/s-2002-34383
PAPER
© Georg Thieme Verlag Stuttgart · New York

Transition Metal-Promoted Synthesis of Functionalized and Unfunctionalized Pyridylallenes

Axel Jansen, Norbert Krause*
Organic Chemistry II, Dortmund University, 44221 Dortmund, Germany
Fax: +49(231)7553884; e-Mail: norbert.krause@uni-dortmund.de;
Further Information

Publication History

Received 14 June 2002
Publication Date:
26 September 2002 (online)

Abstract

The SN2′-substitution of several functionalized and unfunctionalized pyridyl-substituted propargylic acetates with the magnesium cuprate MeMgCl·CuI·LiBr and with phenylzinc chloride in the presence of catalytic amounts of Pd(PPh3)4 is examined. The copper-mediated substitution gives the desired pyridylallenes with good yield only if chelate formation between substrate and cuprate is not possible. In contrast, both chelating and non-chelating propargylic acetates can be converted efficiently into the corresponding pyridyl allenes under palladium catalysis.