Abstract
Rh-catalysed conjugate additions of 2-aminophenyl boronic acid derivatives were exploited in diastereoselective and asymmetric syntheses of tetrahydroquinolines. In both cases, combinatorial variation of the substitution of the tetrahydroquinoline ring system was possible.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Catalysis
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Chemistry Techniques, Synthetic / methods*
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Quinolines / chemical synthesis*
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Rhodium / chemistry*
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Rhodium / metabolism*
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Stereoisomerism
Substances
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Quinolines
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1,2,3,4-tetrahydroquinoline
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Rhodium