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Volumn 45, Issue 11, 1997, Pages 1729-1733

Preparation of cyclic α-hydroxy ketones from δ- and ε-keto acids induced by the generation of a novel acyl anion equivalent from the carboxyl group

Author keywords

Acyl tributylphosphonium ion; Acyl union equivalent; Carboxylic acid; Electrochemical cyclization; Tributylphosphine; hydroxy ketone

Indexed keywords

AROMATIC COMPOUND; CARBOXYL GROUP; CARBOXYLIC ACID; GRAPHITE; KETONE DERIVATIVE; OXOACID; PLATINUM; TRIBUTYL PHOSPHATE;

EID: 0031392175     PISSN: 00092363     EISSN: None     Source Type: Journal    
DOI: 10.1248/cpb.45.1729     Document Type: Article
Times cited : (9)

References (23)
  • 1
    • 3643063002 scopus 로고    scopus 로고
    • This paper is dedicated to Professor Hans J. Schäfer on the occasion of his 60th birthday
    • This paper is dedicated to Professor Hans J. Schäfer on the occasion of his 60th birthday.
  • 2
    • 0006142761 scopus 로고
    • Acyl anion equivalents, for example: Lever O. W., Jr., Tetrahedron, 32, 1943-1971 (1976); Grobel B. T., Seebach D., Synthesis, 1977, 357-402; Martin S. F., ibid., 1979, 633-665; Hase T. A., Koskimies J. K., Aldrichimica Acta, 15, 35-41 (1982); Murata Y., Inomata K., Kinoshita H., Kotake H., Bull. Chem. Soc. Jpn., 56, 2539-2540 (1983); Soderquist J. A., Miranda E. I., Tetrahedron Lett., 27, 6305-6306 (1986); Thurkauf A., Hillery P., Jacobson A. E., Rice K. C., J. Org. Chem., 52, 5466-5467 (1987); Acyl anions, for example: Hiiro T., Morita Y., Inoue T., Kambe N., Ogawa A., Ryu I., Sonoda N., J. Am. Chem. Soc., 112, 455-457 (1990); Collin J., Namy J.-L., Dallemer F., Kagan H. B., J. Org. Chem., 56, 3118-3122 (1991); Namy J.-L., Colomb M., Kagan H. B., Tetrahedron Lett., 35, 1723-1726 (1994).
    • (1976) Tetrahedron , vol.32 , pp. 1943-1971
    • Lever Jr., O.W.1
  • 3
    • 84989423687 scopus 로고    scopus 로고
    • Acyl anion equivalents, for example: Lever O. W., Jr., Tetrahedron, 32, 1943-1971 (1976); Grobel B. T., Seebach D., Synthesis, 1977, 357-402; Martin S. F., ibid., 1979, 633-665; Hase T. A., Koskimies J. K., Aldrichimica Acta, 15, 35-41 (1982); Murata Y., Inomata K., Kinoshita H., Kotake H., Bull. Chem. Soc. Jpn., 56, 2539-2540 (1983); Soderquist J. A., Miranda E. I., Tetrahedron Lett., 27, 6305-6306 (1986); Thurkauf A., Hillery P., Jacobson A. E., Rice K. C., J. Org. Chem., 52, 5466-5467 (1987); Acyl anions, for example: Hiiro T., Morita Y., Inoue T., Kambe N., Ogawa A., Ryu I., Sonoda N., J. Am. Chem. Soc., 112, 455-457 (1990); Collin J., Namy J.-L., Dallemer F., Kagan H. B., J. Org. Chem., 56, 3118-3122 (1991); Namy J.-L., Colomb M., Kagan H. B., Tetrahedron Lett., 35, 1723-1726 (1994).
    • Synthesis , vol.1977 , pp. 357-402
    • Grobel, B.T.1    Seebach, D.2
  • 4
    • 85066912042 scopus 로고    scopus 로고
    • Acyl anion equivalents, for example: Lever O. W., Jr., Tetrahedron, 32, 1943-1971 (1976); Grobel B. T., Seebach D., Synthesis, 1977, 357-402; Martin S. F., ibid., 1979, 633-665; Hase T. A., Koskimies J. K., Aldrichimica Acta, 15, 35-41 (1982); Murata Y., Inomata K., Kinoshita H., Kotake H., Bull. Chem. Soc. Jpn., 56, 2539-2540 (1983); Soderquist J. A., Miranda E. I., Tetrahedron Lett., 27, 6305-6306 (1986); Thurkauf A., Hillery P., Jacobson A. E., Rice K. C., J. Org. Chem., 52, 5466-5467 (1987); Acyl anions, for example: Hiiro T., Morita Y., Inoue T., Kambe N., Ogawa A., Ryu I., Sonoda N., J. Am. Chem. Soc., 112, 455-457 (1990); Collin J., Namy J.-L., Dallemer F., Kagan H. B., J. Org. Chem., 56, 3118-3122 (1991); Namy J.-L., Colomb M., Kagan H. B., Tetrahedron Lett., 35, 1723-1726 (1994).
    • Synthesis , vol.1979 , pp. 633-665
    • Martin, S.F.1
  • 5
    • 0006142761 scopus 로고
    • Acyl anion equivalents, for example: Lever O. W., Jr., Tetrahedron, 32, 1943-1971 (1976); Grobel B. T., Seebach D., Synthesis, 1977, 357-402; Martin S. F., ibid., 1979, 633-665; Hase T. A., Koskimies J. K., Aldrichimica Acta, 15, 35-41 (1982); Murata Y., Inomata K., Kinoshita H., Kotake H., Bull. Chem. Soc. Jpn., 56, 2539-2540 (1983); Soderquist J. A., Miranda E. I., Tetrahedron Lett., 27, 6305-6306 (1986); Thurkauf A., Hillery P., Jacobson A. E., Rice K. C., J. Org. Chem., 52, 5466-5467 (1987); Acyl anions, for example: Hiiro T., Morita Y., Inoue T., Kambe N., Ogawa A., Ryu I., Sonoda N., J. Am. Chem. Soc., 112, 455-457 (1990); Collin J., Namy J.-L., Dallemer F., Kagan H. B., J. Org. Chem., 56, 3118-3122 (1991); Namy J.-L., Colomb M., Kagan H. B., Tetrahedron Lett., 35, 1723-1726 (1994).
    • (1982) Aldrichimica Acta , vol.15 , pp. 35-41
    • Hase, T.A.1    Koskimies, J.K.2
  • 6
    • 0006142761 scopus 로고
    • Acyl anion equivalents, for example: Lever O. W., Jr., Tetrahedron, 32, 1943-1971 (1976); Grobel B. T., Seebach D., Synthesis, 1977, 357-402; Martin S. F., ibid., 1979, 633-665; Hase T. A., Koskimies J. K., Aldrichimica Acta, 15, 35-41 (1982); Murata Y., Inomata K., Kinoshita H., Kotake H., Bull. Chem. Soc. Jpn., 56, 2539-2540 (1983); Soderquist J. A., Miranda E. I., Tetrahedron Lett., 27, 6305-6306 (1986); Thurkauf A., Hillery P., Jacobson A. E., Rice K. C., J. Org. Chem., 52, 5466-5467 (1987); Acyl anions, for example: Hiiro T., Morita Y., Inoue T., Kambe N., Ogawa A., Ryu I., Sonoda N., J. Am. Chem. Soc., 112, 455-457 (1990); Collin J., Namy J.-L., Dallemer F., Kagan H. B., J. Org. Chem., 56, 3118-3122 (1991); Namy J.-L., Colomb M., Kagan H. B., Tetrahedron Lett., 35, 1723-1726 (1994).
    • (1983) Bull. Chem. Soc. Jpn. , vol.56 , pp. 2539-2540
    • Murata, Y.1    Inomata, K.2    Kinoshita, H.3    Kotake, H.4
  • 7
    • 2942728568 scopus 로고
    • Acyl anion equivalents, for example: Lever O. W., Jr., Tetrahedron, 32, 1943-1971 (1976); Grobel B. T., Seebach D., Synthesis, 1977, 357-402; Martin S. F., ibid., 1979, 633-665; Hase T. A., Koskimies J. K., Aldrichimica Acta, 15, 35-41 (1982); Murata Y., Inomata K., Kinoshita H., Kotake H., Bull. Chem. Soc. Jpn., 56, 2539-2540 (1983); Soderquist J. A., Miranda E. I., Tetrahedron Lett., 27, 6305-6306 (1986); Thurkauf A., Hillery P., Jacobson A. E., Rice K. C., J. Org. Chem., 52, 5466-5467 (1987); Acyl anions, for example: Hiiro T., Morita Y., Inoue T., Kambe N., Ogawa A., Ryu I., Sonoda N., J. Am. Chem. Soc., 112, 455-457 (1990); Collin J., Namy J.-L., Dallemer F., Kagan H. B., J. Org. Chem., 56, 3118-3122 (1991); Namy J.-L., Colomb M., Kagan H. B., Tetrahedron Lett., 35, 1723-1726 (1994).
    • (1986) Tetrahedron Lett. , vol.27 , pp. 6305-6306
    • Soderquist, J.A.1    Miranda, E.I.2
  • 8
    • 0000791751 scopus 로고
    • Acyl anion equivalents, for example: Lever O. W., Jr., Tetrahedron, 32, 1943-1971 (1976); Grobel B. T., Seebach D., Synthesis, 1977, 357-402; Martin S. F., ibid., 1979, 633-665; Hase T. A., Koskimies J. K., Aldrichimica Acta, 15, 35-41 (1982); Murata Y., Inomata K., Kinoshita H., Kotake H., Bull. Chem. Soc. Jpn., 56, 2539-2540 (1983); Soderquist J. A., Miranda E. I., Tetrahedron Lett., 27, 6305-6306 (1986); Thurkauf A., Hillery P., Jacobson A. E., Rice K. C., J. Org. Chem., 52, 5466-5467 (1987); Acyl anions, for example: Hiiro T., Morita Y., Inoue T., Kambe N., Ogawa A., Ryu I., Sonoda N., J. Am. Chem. Soc., 112, 455-457 (1990); Collin J., Namy J.-L., Dallemer F., Kagan H. B., J. Org. Chem., 56, 3118-3122 (1991); Namy J.-L., Colomb M., Kagan H. B., Tetrahedron Lett., 35, 1723-1726 (1994).
    • (1987) J. Org. Chem. , vol.52 , pp. 5466-5467
    • Thurkauf, A.1    Hillery, P.2    Jacobson, A.E.3    Rice, K.C.4
  • 9
    • 0025274907 scopus 로고
    • Acyl anion equivalents, for example: Lever O. W., Jr., Tetrahedron, 32, 1943-1971 (1976); Grobel B. T., Seebach D., Synthesis, 1977, 357-402; Martin S. F., ibid., 1979, 633-665; Hase T. A., Koskimies J. K., Aldrichimica Acta, 15, 35-41 (1982); Murata Y., Inomata K., Kinoshita H., Kotake H., Bull. Chem. Soc. Jpn., 56, 2539-2540 (1983); Soderquist J. A., Miranda E. I., Tetrahedron Lett., 27, 6305-6306 (1986); Thurkauf A., Hillery P., Jacobson A. E., Rice K. C., J. Org. Chem., 52, 5466-5467 (1987); Acyl anions, for example: Hiiro T., Morita Y., Inoue T., Kambe N., Ogawa A., Ryu I., Sonoda N., J. Am. Chem. Soc., 112, 455-457 (1990); Collin J., Namy J.-L., Dallemer F., Kagan H. B., J. Org. Chem., 56, 3118-3122 (1991); Namy J.-L., Colomb M., Kagan H. B., Tetrahedron Lett., 35, 1723-1726 (1994).
    • (1990) J. Am. Chem. Soc. , vol.112 , pp. 455-457
    • Hiiro, T.1    Morita, Y.2    Inoue, T.3    Kambe, N.4    Ogawa, A.5    Ryu, I.6    Sonoda, N.7
  • 10
    • 0001490955 scopus 로고
    • Acyl anion equivalents, for example: Lever O. W., Jr., Tetrahedron, 32, 1943-1971 (1976); Grobel B. T., Seebach D., Synthesis, 1977, 357-402; Martin S. F., ibid., 1979, 633-665; Hase T. A., Koskimies J. K., Aldrichimica Acta, 15, 35-41 (1982); Murata Y., Inomata K., Kinoshita H., Kotake H., Bull. Chem. Soc. Jpn., 56, 2539-2540 (1983); Soderquist J. A., Miranda E. I., Tetrahedron Lett., 27, 6305-6306 (1986); Thurkauf A., Hillery P., Jacobson A. E., Rice K. C., J. Org. Chem., 52, 5466-5467 (1987); Acyl anions, for example: Hiiro T., Morita Y., Inoue T., Kambe N., Ogawa A., Ryu I., Sonoda N., J. Am. Chem. Soc., 112, 455-457 (1990); Collin J., Namy J.-L., Dallemer F., Kagan H. B., J. Org. Chem., 56, 3118-3122 (1991); Namy J.-L., Colomb M., Kagan H. B., Tetrahedron Lett., 35, 1723-1726 (1994).
    • (1991) J. Org. Chem. , vol.56 , pp. 3118-3122
    • Collin, J.1    Namy, J.-L.2    Dallemer, F.3    Kagan, H.B.4
  • 11
    • 0028212706 scopus 로고
    • Acyl anion equivalents, for example: Lever O. W., Jr., Tetrahedron, 32, 1943-1971 (1976); Grobel B. T., Seebach D., Synthesis, 1977, 357-402; Martin S. F., ibid., 1979, 633-665; Hase T. A., Koskimies J. K., Aldrichimica Acta, 15, 35-41 (1982); Murata Y., Inomata K., Kinoshita H., Kotake H., Bull. Chem. Soc. Jpn., 56, 2539-2540 (1983); Soderquist J. A., Miranda E. I., Tetrahedron Lett., 27, 6305-6306 (1986); Thurkauf A., Hillery P., Jacobson A. E., Rice K. C., J. Org. Chem., 52, 5466-5467 (1987); Acyl anions, for example: Hiiro T., Morita Y., Inoue T., Kambe N., Ogawa A., Ryu I., Sonoda N., J. Am. Chem. Soc., 112, 455-457 (1990); Collin J., Namy J.-L., Dallemer F., Kagan H. B., J. Org. Chem., 56, 3118-3122 (1991); Namy J.-L., Colomb M., Kagan H. B., Tetrahedron Lett., 35, 1723-1726 (1994).
    • (1994) Tetrahedron Lett. , vol.35 , pp. 1723-1726
    • Namy, J.-L.1    Colomb, M.2    Kagan, H.B.3


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