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(i) Matthews, D. P.; Miller, S. C.; Jarvi, E. T.; Sabol, J. S.; McCarthy, J. R. Tetrahedron Lett. 1993, 34, 3057-3060.
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(a) Bey, P.; McCarthy, J. R.; McDonald, I. A. In Effects of Selective Fluorination on Reactivity; Welch, J. T., Ed.; ACS Symposium Series 456; American Chemical Society; Washington, DC, 1991; 105-133.
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(a) Resnati, G. Tetrahedron 1993, 49, 9385-9445.
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For a recent report on the use of this reaction for the preparation of a fluoromethyl group via a fluoro olefin, see: Schmidt, C. Synlett 1994, 241-242.
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We have recently published an example of the synthesis of 1-fluoro olefins, see; McCarthy, J, R.; Matthews, D. P.; Paolini, J. P. Org. Syn. 1994, 72, 216-224.
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Org. Syn.
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McCarthy, J.R.1
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For an alternate synthesis of 34, see: Matthews, D. P.; Persichetti, R. A.; Sabol, J. S.; Stewart, K. T.; McCarthy, J. R. Nucleosides & Nucleotides 1993, 12, 115-123.
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Nucleosides & Nucleotides
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(b) McCarthy, J. R.; Matthews, D. P.; Paolini, J. P. Org. Syn. 1994, 72, 209-215.
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McCarthy, J. R.; Sunkara, P. S. In: Chemical and Structural Approaches to Rational Drug Design; Weiner, D. B.; Williams, W. B.; Ed.; CRC Press, Boca Raton, 1995, pp 3-34.
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(b) Jarvi, E. T.; McCarthy, J. R.; Mehdi, S.; Matthews, D. P.; Edwards, M. L.; Prakash, N. J.; Bowlin, T. L.; Sunkara, P. S.; Bey, P. J. Med. Chem. 1991, 34, 647-656.
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For a leading reference on radical reactions with tributyltin hydride see: Neumann, W. P. Synthesis 1987, 665-683.
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Matsuda, A.; Itoh, H.; Takenuki, K.; Susaki, T.; Ueda, T. Chem. Pharm. Bull. 1988, 36, 945-953.
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Huffman, J. C., Indiana University, will be published.
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Bitonti, A. J.; Dumont, J. A.; Bush, T. L.; Cashman, E. A.; Cross-Doersen, D. E.; Wright, P. S.; Matthews, D. P.; McCarthy, J. R. ; Kaplan, D. A. Cancer Research, 1994, 54, 1485-1490.
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Cancer Research
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For inhibitors of alanine racemase, see: (a) Walsh, C. Enzymatic Reaction Mechanisms, W. H. Freemen and Co., San Francisco 1979, pp. 798-799.
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