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6
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85038063951
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For all optically active compounds reported in this paper, the (-)-isomers are (2R,6R,11R) and the (+)-isomers are (2S,6S,11S)
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For all optically active compounds reported in this paper, the (-)-isomers are (2R,6R,11R) and the (+)-isomers are (2S,6S,11S).
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7
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0024385291
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9
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10
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0029096568
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11
-
-
85038061639
-
-
Proton NMR, IR, MS were consistent with the assigned structures of all new compounds. C, H, and N elemental analyses were obtained for all new targets and most intermediates and were within ±0.4% of theoretical values
-
Proton NMR, IR, MS were consistent with the assigned structures of all new compounds. C, H, and N elemental analyses were obtained for all new targets and most intermediates and were within ±0.4% of theoretical values.
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-
-
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15
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85038061717
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-
note
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2O: C, 81.77; H, 8.58; N, 7.95. Found: C, 81.60; H, 8.64; N, 7.78. This reaction was performed on a larger scale (3-fold) giving a similar yield of (±)-10 (mp, 144-146 °C).
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-
-
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16
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85038062065
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3-Tris(dibenzylideneacetone)dipalladium(0); DPPF-1,1′-bis(diphenyl-phosphino)-ferrocene
-
3-Tris(dibenzylideneacetone)dipalladium(0); DPPF-1,1′-bis(diphenyl-phosphino)-ferrocene.
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-
-
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17
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0030873988
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0000092188
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Wolff, M. E., Ed.; John Wiley & Sons: New York
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