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note
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Our findings do not permit us to differentiate this effect from stabilizing interactions that may be derived from the π-electrons localized at C(5) within the bicyclomycin derivative and the receptor.
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0003450582
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Academic Press: San Diego
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For a discussion of enzyme irreversible inactivators, see: (a) Silverman, R. B. The Organic Chemistry of Drug Design and Drug Action; Academic Press: San Diego, 1992; pp 178-219. (b) Bayley, H.; Staros, J. V. Photoaffinity Labeling and Related Techniques. In Azides and Nitrenes: Reactivity and Utility; Scriven, E. F. V., Ed.; Academic Press: Orlando, 1984; pp 433-490. (c) Fleming, S. A. Tetrahedron 1995, 51, 12479-12520.
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31
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0001732094
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Photoaffinity Labeling and Related Techniques
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Scriven, E. F. V., Ed.; Academic Press: Orlando
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For a discussion of enzyme irreversible inactivators, see: (a) Silverman, R. B. The Organic Chemistry of Drug Design and Drug Action; Academic Press: San Diego, 1992; pp 178-219. (b) Bayley, H.; Staros, J. V. Photoaffinity Labeling and Related Techniques. In Azides and Nitrenes: Reactivity and Utility; Scriven, E. F. V., Ed.; Academic Press: Orlando, 1984; pp 433-490. (c) Fleming, S. A. Tetrahedron 1995, 51, 12479-12520.
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For a discussion of enzyme irreversible inactivators, see: (a) Silverman, R. B. The Organic Chemistry of Drug Design and Drug Action; Academic Press: San Diego, 1992; pp 178-219. (b) Bayley, H.; Staros, J. V. Photoaffinity Labeling and Related Techniques. In Azides and Nitrenes: Reactivity and Utility; Scriven, E. F. V., Ed.; Academic Press: Orlando, 1984; pp 433-490. (c) Fleming, S. A. Tetrahedron 1995, 51, 12479-12520.
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