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0035898426
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(E)-α,β-Unsaturated amides 1 were prepared following the methods described in: (a) Concellón, J. M.; Pérez-Andrés, J. A.; Rodríguez-Solla, H. Chem. Eur. J. 2001, 7, 3062-3068.
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(E)-α,β-Unsaturated amides 1 were prepared following the methods described in: (a) Concellón, J. M.; Pérez-Andrés, J. A.; Rodríguez-Solla, H. Chem. Eur. J. 2001, 7, 3062-3068.
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(b) Concellón, J. M.; Rodríguez-Solla, H.; Díaz, P. J. Org. Chem. 2007, 72, 7974-7979.
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Rodríguez-Solla, H.2
Díaz, P.3
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28
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38749124293
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In the case of compound 3b although dr, 95/5 the reaction was also completely stereoselective since the E/Z ratio of the starting α,β- unsaturated amide was 95/5
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In the case of compound 3b although dr = 95/5 the reaction was also completely stereoselective since the E/Z ratio of the starting α,β- unsaturated amide was 95/5.
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29
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38749109926
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CCDC 630875 contains the supplementary crystallographic data for compound 3e. These data can be obtained free of charge via: www.ccdc.cam.ac.uk/ conts/retrieving.html (or the Cambridge Data Center, 12 Union Road, Cambridge CB21EZ, UK; fax (+44)1223-336-033, or e-mail deposit@ccdc.cam.ac.uk).
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CCDC 630875 contains the supplementary crystallographic data for compound 3e. These data can be obtained free of charge via: www.ccdc.cam.ac.uk/ conts/retrieving.html (or the Cambridge Data Center, 12 Union Road, Cambridge CB21EZ, UK; fax (+44)1223-336-033, or e-mail deposit@ccdc.cam.ac.uk).
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30
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38749128642
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(Z)-N,N-Dimethyloct-2-enamide was obtained from the catalytic Lindlar's hydrogenation of N,N-dimethyloct-2-inamide.
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(Z)-N,N-Dimethyloct-2-enamide was obtained from the catalytic Lindlar's hydrogenation of N,N-dimethyloct-2-inamide.
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31
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38749112470
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The use of diamines, TMEDA or TEEDA, was necessary to carry out the silylcyclopropanation described in reference 6.
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The use of diamines, TMEDA or TEEDA, was necessary to carry out the silylcyclopropanation described in reference 6.
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32
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0000429936
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