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1H NMR spectrum and this correlation has been used to compare the relative acid strength of various Lewis acids. For details, see: and Ref. 3b.
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1H NMR spectrum and this correlation has been used to compare the relative acid strength of various Lewis acids. For details, see: Childs, R. F.; Mulholland, D. L.; Nixon, A. Can. J. Chem. 1982, 60, 801 and Ref. 3b.
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0009623245
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2 using hexane:EA (20:1) as eluent. Yield=0.60 g (83%)
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2 using hexane:EA (20:1) as eluent. Yield=0.60 g (83%).
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24
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0009567685
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in preparation
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Fuh, Y.-S.; Chaen, M.-C.; Tsai, L.-C.; Hu, W.-R; Yu, S. J. in preparation.
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0009579289
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2 might be formed from the reaction of 1 and water. The resulting metal species was slightly soluble in water. For examples of documented transition metal aqua complexes as efficient D-A catalysts, see Refs. 4a-c and 6e
-
2 might be formed from the reaction of 1 and water. The resulting metal species was slightly soluble in water. For examples of documented transition metal aqua complexes as efficient D-A catalysts, see Refs. 4a-c and 6e.
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0342713055
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There was no polymeric materials observed by the NMR nor detectable precipitates formed during the course of 1- catalyzed D-A reactions of cyclopentadiene and cyclohexadiene systems
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There was no polymeric materials observed by the NMR nor detectable precipitates formed during the course of 1- catalyzed D-A reactions of cyclopentadiene and cyclohexadiene systems.
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