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Review
. 2005 Feb 4;44(7):1012-1044.
doi: 10.1002/anie.200460864.

Chasing molecules that were never there: misassigned natural products and the role of chemical synthesis in modern structure elucidation

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Review

Chasing molecules that were never there: misassigned natural products and the role of chemical synthesis in modern structure elucidation

K C Nicolaou et al. Angew Chem Int Ed Engl. .

Erratum in

  • Angew Chem Int Ed Engl. 2005 Mar 29;44(14):2050

Abstract

Over the course of the past half century, the structural elucidation of unknown natural products has undergone a tremendous revolution. Before World War II, a chemist would have relied almost exclusively on the art of chemical synthesis, primarily in the form of degradation and derivatization reactions, to develop and test structural hypotheses in a process that often took years to complete when grams of material were available. Today, a battery of advanced spectroscopic methods, such as multidimensional NMR spectroscopy and high-resolution mass spectrometry, not to mention X-ray crystallography, exist for the expeditious assignment of structures to highly complex molecules isolated from nature in milligram or sub-milligram quantities. In fact, it could be argued that the characterization of natural products has become a routine task, one which no longer even requires a reaction flask! This Review makes the case that imaginative detective work and chemical synthesis still have important roles to play in the process of solving nature's most intriguing molecular puzzles.

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References

    1. To explore these assignments further, see the Nobel Prize website: http://www.nobel.se/chemistry.
    1. J. D. Bernal, Nature 1932, 129, 721.
    1. None
    1. P. Rabe, Ber. Dtsch. Chem. Ges. 1908, 41, 62;
    1. P. Rabe, E. Ackerman, W. Schneider, Ber. Dtsch. Chem. Ges. 1907, 40, 3655; for the first total synthesis of quinine, see:

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