Syntheses and Proton Magnetic Resonance Studies at 300 MHz of Two New Bromopentachlorocyclohexanes and Three New Bromotrichlorocyclohexenes |
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Authors: | Yuzuru Sanemitsu Norio Kurihara Minoru Nakajima G E McCasland L F Johnson L C Carey |
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Institution: | 1. Department of Agricultural Chemistry, Kyoto University, Kyoto;2. Department of Chemistry, University of San Francisco, San Francisco, California, 94117, U.S.A.;3. Varian Associates, Palo Alto, California, 94303, U.S.A. |
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Abstract: | Two diastereomers of 6-bromo-1, 2, 3, 4, 5-pentachlorocyclohexane were synthesized from the dl (36/45)-diastereomer of 3, 4, 5, 6-tetrachlorocyclohexene (α-BTC) and the dl (346/5)-diastereomer (γ-BTC) by several stepwise routes. Both of these new products were shown to have the configuration of lindane by NMR studies at 300 MHz and by the synthetic routes. Three diastereomers of 6-bromo-3, 4, 5-trichlorocyclohexene were also prepared and the configurations determined partly by means of 300 MHz NMR. |
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Keywords: | catechins epigallocatechin gallate Bacillus subtilis |
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