By Zvi Rappoport, Joel F. Liebman
Targeting a huge category of compounds in natural synthesis, this article good points contributions via prime specialists, and supplies the standard anticipated from the “Patai Series.”
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Extra info for The chemistry of hydroxylamines, oximes, and hydroxamic acids
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B. Hydroxylamine Configurations . . . . . . C. Oximes . . . . . . . . . . . . . . D. Hydroxamic Acids . . . . . . . . . . IV. SUMMARY . . . . . . . . . . . . . V. ACKNOWLEDGMENT . . . . . . . . . . VI. REFERENCES . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Murray, Z. Peralta-Inga, P. Politzer, K. Ekanayake and P. LeBreton, Int. J. , Biophys. , 83, 245 (2001). P. Jin, J. S. Murray and P. Politzer, Comp. , 3, 373 (2007). P. Politzer, J. S. Murray and M. C. Concha, J. Phys. Org. , 21, 155 (2008). A. Bondi, J. Phys. , 68, 441 (1964). D. R. , CRC Press, Boca Raton, 2006. F. H. Allen, O. Kennard, D. G. Watson, L. Brammer, A. G. Orpen and R. Taylor, J. Chem. , Perkin Trans. 2, S1 (1987). P. Politzer, J. S. Murray and M. C. Concha, Int. J. , 88, 19 (2002).
C. Hydroxylamine Configuration and Conformations D. Oximes . . . . . . . . . . . . . . E. Hydroxamic Acids . . . . . . . . . . III. CRYSTAL PHASE STRUCTURES . . . . . . A. N−O Bond Lengths . . . . . . . . . . B. Hydroxylamine Configurations . . . . . . C. Oximes . . . . . . . . . . . . . . D. Hydroxamic Acids . . . . . . . . . . IV. SUMMARY . . . . . . . . . . . . . V. ACKNOWLEDGMENT . . . . . . . . . . VI.