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+ cation and structurally similar calix[4]arenes. The cation was found encapsulated within the cavity (X-ray analysis). See: Rathore, R.; Lindeman, S. V.; Rao, K. S. S.; Sun, D.; Kochi, J. K. Angew. Chem., Int. Ed. 2000, 39, 2123-2127.
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24
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0141549224
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note
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8Sn: C, 61.04; H, 7.83; N, 2.09. Found: C, 60.96; H, 7.88; N, 2.09.
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26
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0141772553
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note
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1H NMR spectroscopy and, in some cases, separated by preparative TLC. All runs were performed at least in duplicate.
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27
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0141772554
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note
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3, similar to the protocol reported in ref 16a. From both methods, the spectral and TLC data for N-nitroso compounds 4a-e were identical and in agreement with published data; see ref 16c-e and Supporting Information. Caution: N-Nitrosoamides are carcinogens and should be treated with extreme care.
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29
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0001587728
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For rare examples of steric inhibition of N-nitrosation with crowded amides, see: (g) Garcia, J.; Gonzalez, J.; Segura, R.; Vilarrasa, J. Tetrahedron 1984, 40, 3121-3127. (h) Evans, D. A.; Carter, P. H.; Dinsmore, C. J.; Barrow, J. C.; Katz, J. L.; Kung, D. W. Tetrahedron Lett. 1997, 38, 4535-4538.
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35
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0030912448
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For rare examples of steric inhibition of N-nitrosation with crowded amides, see: (g) Garcia, J.; Gonzalez, J.; Segura, R.; Vilarrasa, J. Tetrahedron 1984, 40, 3121-3127. (h) Evans, D. A.; Carter, P. H.; Dinsmore, C. J.; Barrow, J. C.; Katz, J. L.; Kung, D. W. Tetrahedron Lett. 1997, 38, 4535-4538.
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36
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0037012822
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and references therein
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Darbeau, R. W.; Pease, R. S.; Perez, E. V. J. Org. Chem. 2002, 67, 2942-2947 and references therein.
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37
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0024286073
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note
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1H NMR. Moreover, if the nitrosation proceeded via the cis conformers, there should not be any preferences in reactivities for amides with different R′-groups, as they are positioned far away from the calixarene cavity.
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