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Volumn 105, Issue 20, 1983, Pages 6243-6248

Aliphatic Hydroxylation Catalyzed by Iron Porphyrin Complexes

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Indexed keywords

ORGANIC COMPOUNDS;

EID: 0021095665     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja00358a009     Document Type: Article
Times cited : (444)

References (72)
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    • (1980) , pp. 146
    • Groves, J.T.1    Spiro, T.G.2
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    • First presented at the Symposium on Biochemical and Clinical Aspects of Oxygen, Colorado State University
    • First presented at the Symposium on Biochemical and Clinical Aspects of Oxygen, Colorado State University, Pingree Park Campus, Sept 1978.
    • (1978)
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    • Subsequent to our report on this iron porphyrin-iodosylbenzene reaction, we and others have demonstrated improved yields for hydroxylation with manganese porphyrins
    • Subsequent to our report on this iron porphyrin-iodosylbenzene reaction, we and others have demonstrated improved yields for hydroxylation with manganese porphyrins: Groves, J. T.; Kruper, W. J., Jr.; Haushalter, R. C. J. Am. Chem. Soc. 1980, 102, 6375-6377.
    • (1980) J. Am. Chem. Soc. , vol.102 , pp. 6375-6377
    • Groves, J.T.1    Kruper, W.J.2    Haushalter, R.C.3
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    • Several examples of oxidative addition of low-valent metal species into unactivated C-H bonds have been reported
    • Several examples of oxidative addition of low-valent metal species into unactivated C-H bonds have been reported: Halle, L. F.; Armentrout, P. B.; Beauchamp, J. L. J. Am. Chem. Soc. 1981, 103, 962-963.
    • (1981) J. Am. Chem. Soc. , vol.103 , pp. 962-963
    • Halle, L.F.1    Armentrout, P.B.2    Beauchamp, J.L.3
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    • Oxidation in Organic Chemistry, Part A
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    • An iron(IV) porphyrin species has recently been described:
    • An iron(IV) porphyrin species has recently been described: Chin, D.-H.; Balch, A. L.; LaMar, G.N. J. Am. Chem. Soc. 1980, 102, 1446-1448.
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    • The Porphyrins
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    • (1979) , vol.4
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    • Benyon, J. H.; Saunders, R. A.; Williams, A. E. Appl. Spectrosc. 1960, 14, 95) for mass spectra of the decalones. The identity of the decalols can be inferred from the decalone mass spectra.
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    • A sample of the 2-norcaranol was obtained from J. Kruper. It was synthesized by the method of Dauben).
    • A sample of the 2-norcaranol was obtained from J. Kruper. It was synthesized by the method of Dauben (Dauben, W. G.; Berezin, G. H. J. Am. Chem. Soc. 1963, 85, 468-472).
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