Synthesis 2001; 2001(1): 0145-0149
DOI: 10.1055/s-2001-9751
paper
© Georg Thieme Verlag, Rüdigerstr. 14, 70469 Stuttgart, Germany. All rights reserved. This journal, including all individual contributions and illustrations published therein, is legally protected by copyright for the duration of the copyright period. Any use, exploitation or commercialization outside the narrow limits set by copyright legislation, without the publisher's consent, is illegal and liable to criminal prosecution. This applies in particular to photostat reproduction, copying, cyclostyling, mimeographing or duplication of any kind, translating, preparation of microfilms, and electronic data processing and storage.

Facile Synthesis of Aliphatic Esters, Malonates and Phenylsulfonyl Esters Using Copper-Catalyzed Addition of Methallyl Grignard Reagent to Activated Cyclopropanes

Igor Prowotorow* , Jerzy Wicha, Koichi Mikami
  • *Institute of Organic Chemistry, Polish Academy of Sciences, POB 58, PL 01-224 Warsaw 42, Poland; Fax +48(22)6 32 66 81; E-mail: jwichaichf.edu.pl
Further Information

Publication History

Publication Date:
31 December 2001 (online)

Copper-mediated conjugate addition of allylic Grignard reagents to activated cyclopropane derivatives was studied. Unsaturated esters, malonates and phenylsulfonyl esters 2a-d were synthesized from the respective cyclopropanes 1a-d and methallylmagnesium chloride.

    >