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(a) Leibowitz, M. D.; Fievet, C.; Hennuyer, N.; Peinado-Onsurbe, J.; Duez, H.; Berger, J.; Cullinan, C. A.; Sparrow, C. P.; Baffic, J.; Berger, G. D.; Santini, C.; Marquis, R. W.; Tolman, R. L.; Smith, R. G.; Moller, D. E.; Auwerx, J. FEBS Lett. 2000, 473, 333.
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(b) Shi, Y.; Hon, M.; Evans, R. M. Proc. Natl. Acad. Sci. USA 2002, 99, 2613.
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(c) Oliver, W. R., Jr.; Shenk, J. L.; Snaith, M. R.; Russell, C. S.; Plunket, K. D.; Bodkin, N. L.; Lewis, M. C.; Winega, D. A.; Sznaidman, M. L.; Lambert, M. H.; Xu, H. E.; Sternbach, D. D.; Kliewer, S. A.; Hansen, B. C.; Willson, T. M Proc. Natl. Acad. Sci. USA 2001, 98, 5306.
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341 describes this method applied to a similar amide
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Suzuki, H.; Kimura, Y. J. Fluorine Chem. 1991, 52, 341 (describes this method applied to a similar amide).
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The dipolar addition reaction of nitrile sulfides and ethyl cyanoformate has been described in: Howe, R. K.; Franz, J. E. J. Org. Chem. 1974, 39, 962.
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The dipolar addition reaction of nitrile sulfides and ethyl cyanoformate has been described in: Howe, R. K.; Franz, J. E. J. Org. Chem. 1974, 39, 962.
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8
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(b) Gillespie, J. S., Jr.; Acharya, S. P.; Shamblee, D. A.; Davis, R. E Tetrahedron 1975, 31, 3.
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33749018785
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For another alternative to the conventional Baeyer-Villiger reaction see:, and references cited therein
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(d) For another alternative to the conventional Baeyer-Villiger reaction see: Yoshida, A.; Hao, X.; Yamazaki, O.; Nishikido, J. QSAR Comb. Sci. 2006, 25, 697 and references cited therein.
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(a) Stanton, J. L.; Cahill, E.; Dotson, R.; Tan, J.; Tomaselli, H. C.; Wasvary, J. M.; Stephan, Z. F.; Steele, R. E. Bioorg. Med. Chem. Lett. 2000, 10, 1661.
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(b) Mazzinni, F.; Alpi, E.; Salvadori, P.; Netscher, T. Eur. J. Org. Chem. 2003, 2840.
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Other phenol blocking methods can be considered:Masada, H., Oishi, Y. Chem. Lett. 1978, 57.
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(a) Other phenol blocking methods can be considered:Masada, H., Oishi, Y. Chem. Lett. 1978, 57.
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