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Synthesis 2007(4): 572-582
DOI: 10.1055/s-2007-965897
DOI: 10.1055/s-2007-965897
PAPER
© Georg Thieme Verlag Stuttgart · New York
Synthesis of Chiral C 2-Symmetric Methylene- and Boron-Bridged Bis(imidazolines)
Further Information
Received
25 July 2006
Publication Date:
18 January 2007 (online)
Publication History
Publication Date:
18 January 2007 (online)
Abstract
A series of C 2-symmetric boron-bridged bis(imidazolines) was obtained by lithiation of 2-imidazolines and subsequent reaction with dialkyl- or diarylhaloboranes. The corresponding 2-imidazolines were prepared by an efficient four-step sequence starting from N-tert-butoxycarbonyl-protected α-amino acids. C 2-Symmetric methylenebis(imidazolines) were readily synthesized from chiral diamines by condensation with diethyl malonimidate. The bis(imidazolines) were used as ligands in the enantioselective cyclopropanation of styrene and allylic oxidation of cyclic alkenes.
Key words
chiral imidazolines - bis(imidazolines) - asymmetric catalysis - chiral ligands - copper complexes
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