An effect of application of chiral aluminium alkoxides and amides as adducts to zirconium catalyzed carbo- and cycloalumination of olefins |
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Authors: | Leonard M Khalilov Ludmila V Parfenova Askhat G Ibragimov Usein M Dzhemilev |
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Institution: | a Institute of Petrochemistry and Catalysis, Bashkortostan Republic Academy of Science and Ufa Scientific Centre of RAS, Prospect Oktyabrya, 141, Ufa 450075, Russian Federation b Ecole Nationale Superieure de Chimie de Paris, France c Department of Chemistry, Moscow State University, V-234, Moscow, GSP 199889, Russian Federation |
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Abstract: | This paper is dedicated to a study of properties of the following novel optically active organoaluminium compounds (OACs): (1S,2S)-l,7,7-trimethyl-2-(dialkylalumina)oxy]-bicyclo2.2.1]heptanes and (1S)-N-(dialkylalumina)-6,7-dimethoxy-1-methyl-1,2,3,4- tetrahydroisoquinolines. The synthesis of the chiral OACs was carried out in the reaction of either natural camphor or salsolidine with both AlEt3 and i-Bu2AlH. The main goal of the research was to investigate the stereodifferentiating activity of the chiral OACs in the olefin carbo- and cycloalumination reactions, catalyzed by Cp2ZrCl2. |
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Keywords: | Chiral organoaluminium compounds Cycloalumination Carboalumination Camphor Salsolidine Optically active shift reagents |
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