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Intermediates and Competing Reactions in the Photodestruction of Indoleacetic Acid

Nature volume 181, pages 895–896 (1958)Cite this article

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References

  1. R F values in isopropanol: 28 per cent ammonia: water, 10 : 1 : 1 (cf. Stowe, B. B., and Thimann, K. V., Arch. Biochem. Biophys., 51, 499; 1954): indole-3-acetic acid, 0.26; M′, 0.38; Ehrlichand 2,4-dinitrophenylhydrazine-positive product of indole-3-acetic acid photodestruction, 0.74; indolealdehyde, 0.75; indoleglycolic acid, 0.18; indoleglyoxylic acid, 0.25.

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  2. Fischer, A., Planta, 43, 288 (1954).

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  3. This has been found also by Bentley, J. A., et al., Biochem. J., 64, 44 (1956), and by Greenberg, J. B., Galston, A. W., Shaw, K. N. F., and Armstrong, M. D., Science, 125, 992 (1957).

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  4. Ray, P. M., and Thimann, K. V., Arch. Biochem. Biophys., 64, 175 (1956).

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  5. Stutz, R. E., Plant Physiol. (in the press).

  6. Curry, G. M., Thimann, K. V., and Ray, P. M., Physiol. Plantarum, 9, 429 (1956).

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Author notes

  1. PETER M. RAY: Society of Fellows, Harvard University.

  2. GEORGE M. CURRY: National Science Foundation Postdoctoral Fellow.

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  1. Biological Laboratories, Harvard University,

    PETER M. RAY & GEORGE M. CURRY

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  1. PETER M. RAY
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RAY, P., CURRY, G. Intermediates and Competing Reactions in the Photodestruction of Indoleacetic Acid. Nature 181, 895–896 (1958). https://doi.org/10.1038/181895a0

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