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Communication | Regular issue | Vol 26, No. 4, 1987, pp.929-934
Published online, 1st January, 1970
DOI: 10.3987/R-1987-04-0929
Synthesis of Pyrrolidine Derivatives by Improves Aminoselenation via Addition of Boron Trifluoride Complex of Dihomoallylcuprate to Aldimines Containing α-Hydrogen

Makoto Wada, Hideki Aiura, and Kin-ya Akiba

*Department of Chemistry, Faculty of Science, Hiroshima University, 1-3-1 Kagamiyama, Higashi-Hiroshima, Hiroshima 739-8526, Japan

Abstract

Boron trifluoride complex of magnesium dihomoallylcuprate, (CH2=CHCH2CH2)2CuMgBr.BF3, reacted wlth aldimines containing α-hydrogen to afford the corresponding addltion products in good yields. The addition products were converted to pyrrolidine derivatives by treatment with phenylselenenyl chloride in the presence of trifluoroacetic acid and silica gel.