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Volumn 37, Issue 7, 1972, Pages 930-936

Reduction of Nitroaryls by Dodecacarbonyltriiron-Methanol

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EID: 0001427385     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo00972a002     Document Type: Article
Times cited : (97)

References (32)
  • 1
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    • This work was supported by the National Science Foundation. It was presented at Metrochem ′71, San Juan, Puerto Rico, April 30-May 3, Abstracts of Papers
    • This work was supported by the National Science Foundation. It was presented at Metrochem ′71, San Juan, Puerto Rico, April 30-May 3, 1971, Abstracts of Papers, p 19.
    • (1971) , pp. 19
  • 2
    • 85023248929 scopus 로고
    • Abstracted in part from the Ph. D. Thesis of Lawrence Katz, Adelphi University, April
    • Abstracted in part from the Ph. D. Thesis of Lawrence Katz, Adelphi University, April 1971.
    • (1971)
  • 5
    • 37049043169 scopus 로고
    • these workers describe the reduction of nitromethane with ethanolic solutions of KHFe (CO) 4; methylamine and ferric hydroxide result after 12 hr
    • J. R. Case and M. C. Whiting, J. Chem. Soc., 4632 (1960); these workers describe the reduction of nitromethane with ethanolic solutions of KHFe (CO) 4; methylamine and ferric hydroxide result after 12 hr.
    • (1960) J. Chem. Soc. , pp. 4632
    • Case, J.R.1    Whiting, M.C.2
  • 10
    • 85023235628 scopus 로고
    • We thank Professor G. R. Knox for kindly supplying a sample of 7a and the spectra: λmax (cyclohexane) (ε × 103)
    • We thank Professor G. R. Knox for kindly supplying a sample of 7a and the spectra: λmax (cyclohexane) (ε × 103) 311 (8. 8), 356 (4. 5), 410 (sh) (3. 4), and 519 mμ (2. 3); v (CS2) 2062 (vs), 2043 (vs), 2011 (s), 1979 (sh), 1960cm-1 (sh) (C≡O).
    • (1979)
  • 12
    • 0001435036 scopus 로고
    • and references cited therein.
    • J. E. Kmiecik, J. Org. Chem., 30, 2014 (1965), and references cited therein.
    • (1965) J. Org. Chem. , vol.30 , pp. 2014
    • Kmiecik, J.E.1
  • 13
    • 0011028421 scopus 로고
    • and references cited therein; phenylnitrene inserts into cyclohexane to give N-phenylcyclohexylamine.
    • J. H. Hall, J. W. Hill, and H. Tsai, Tetrahedron Lett., 2211 (1965), and references cited therein; phenylnitrene inserts into cyclohexane to give N-phenylcyclohexylamine.
    • (1965) Tetrahedron Lett. , pp. 2211
    • Hall, J.H.1    Hill, J.W.2    Tsai, H.3
  • 14
    • 0141966931 scopus 로고
    • The structure of the hydrodoundecacarbonyltriferrate anion has been determined: (a)
    • The structure of the hydrodoundecacarbonyltriferrate anion has been determined: (a) L. F. Dahl and J. F. Blount, Inorg. Chem., 4, 1373 (1965)
    • (1965) Inorg. Chem. , vol.4 , pp. 1373
    • Dahl, L.F.1    Blount, J.F.2
  • 19
    • 0004135049 scopus 로고
    • St. Martins Press, New York, N. Y., 92
    • P. L. Pausen, “Organometallic Chemistry,” St. Martins Press, New York, N. Y., 1967, pp 91, 92.
    • (1967) Organometallic Chemistry , pp. 91
    • Pausen, P.L.1
  • 20
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    • Ligand displacement on iron by M+-O- (where M is N, S, P, As) is known; see (a)
    • Ligand displacement on iron by M+-O- (where M is N, S, P, As) is known; see (a) W. Strohmeier, J. F. Guttenberger, and G. Popp, Chem. Ber., 98, 2248 (1965)
    • (1965) Chem. Ber. , vol.98 , pp. 2248
    • Strohmeier, W.1    Guttenberger, J.F.2    Popp, G.3
  • 22
    • 84915427096 scopus 로고
    • I. Wender and P. Pino, Ed., Interscience, New York, N. Y.
    • W. Hubei in “Organic Syntheses via Metal Carbonyls,” I. Wender and P. Pino, Ed., Interscience, New York, N. Y., 1968, p 322.
    • (1968) Organic Syntheses via Metal Carbonyls , pp. 322
    • Hubei, W.1
  • 24
    • 84917841880 scopus 로고
    • prepared photochemically from Fe (CO) 5 and nitrobenzene
    • E. Koerner von Gustorf and M. J. Jun, Z. Naturforsch., 20B, 521 (1965); prepared photochemically from Fe (CO) 5 and nitrobenzene.
    • (1965) Z. Naturforsch. , vol.20B , pp. 521
    • Koerner von Gustorf, E.1    Jun, M.J.2
  • 26
    • 0003031432 scopus 로고
    • The chemistry of such species is unknown; however, organometallic oxo metal complexes are known; see
    • The chemistry of such species is unknown; however, organometallic oxo metal complexes are known; see M. Cousins and M. L. H. Green, J. Chem. Soc., 1567 (1964).
    • (1964) J. Chem. Soc. , pp. 1567
    • Cousins, M.1    Green, M.L.H.2
  • 27
    • 0006954739 scopus 로고
    • English translation by E. D. Morgan, Iliffe Books, London, 134, 266
    • L. Szepesey, “Gas Chromatography,” English translation by E. D. Morgan, Iliffe Books, London, 1970, pp 133, 134, 266.
    • (1970) Gas Chromatography , pp. 133
    • Szepesey, L.1
  • 30
    • 84943059526 scopus 로고
    • N. Rabjohn, Ed., Wiley, New York, N. Y.
    • G. A. Ropp and E. C. Coyner in “Organic Syntheses,” Collect. Vol., 4, N. Rabjohn, Ed., Wiley, New York, N. Y., 1963, p 727.
    • (1963) Organic Syntheses , vol.4 , pp. 727
    • Ropp, G.A.1    Coyner, E.C.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.