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D.A. Leigh, P.J. Lusby, S.J. Teat, A.J. Wilson, and J.K.Y. Wong Angew. Chem., Int. Ed. Engl. 40 2001 1538 1543
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24
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4644265484
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Leigh and co-workers have independently studied and recently reported the synthesis of a [2]rotaxane utilizing a 2,6-pyridinedicarboxamide-based Pd complex, based on a different protocol via macrocyclization A.-M. Fuller, D.A. Leigh, P.J. Lusby, I.D.H. Oswald, S. Parsons, and D.B. Walker Angew. Chem., Int. Ed. Engl. 43 2004 3914 3918
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Walker, D.B.6
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9744254921
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note
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1H NMR, IR, FAB-MS spectra, and elemental analyses
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9744248898
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note
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Compound 3b was prepared by the Sonogashira coupling of 2,6-dibromopyridine and 2-propyne-1-ol
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29
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9744236026
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Compound 3c was prepared from 3,5-dibromopyridine similarly to 3b
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84862482210
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deposit@ccdc.cam.ac.uk
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int = 0.034], R = 0.0540, wR = 0.0740 for 10,995 observed data [I > 3σ(I)], GOF = 1.237
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31
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9744262664
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note
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4-Tris(4-t-butylphenyl)methylphenyl isocyanate was prepared by the reaction of 4-tris(4-t-butylphenyl)methylaniline and triphosgene in refluxing toluene
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32
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0842305885
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Y. Furusho, H. Sasabe, D. Natsui, K. Murakawa, T. Takata, and T. Harada Bull. Chem. Soc. Jpn. 77 2004 179 185
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Bull. Chem. Soc. Jpn.
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Furusho, Y.1
Sasabe, H.2
Natsui, D.3
Murakawa, K.4
Takata, T.5
Harada, T.6
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33
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9744226620
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note
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3.0 (1836.34): C, 75.87; H, 7.36; N, 4.58; found: C, 75.60; H, 7.44; N, 4.41
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34
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9744286430
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note
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1H NMR spectrum was observed for all the signals down to -50°C. This indicates that the macrocyclic component moves along the dumbbell component with a high degree of freedom
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