메뉴 건너뛰기




Volumn 61, Issue 16, 1996, Pages 5435-5439

A convenient one-pot preparative method for 4,5-diarylisoxazoles involving amine exchange reactions

Author keywords

[No Author keywords available]

Indexed keywords


EID: 0000228798     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo960024h     Document Type: Article
Times cited : (93)

References (75)
  • 3
    • 84943418328 scopus 로고
    • Katritzky, A. R., Rees, C. W., Eds.; Pergamon Press: Exeter
    • For a review see: Lang, S. A.; Lin, Y. in Comprehensive Heterocyclic Chemistry; Katritzky, A. R., Rees, C. W., Eds.; Pergamon Press: Exeter, 1984; Vol. 6, pp 1-130.
    • (1984) Comprehensive Heterocyclic Chemistry , vol.6 , pp. 1-130
    • Lang, S.A.1    Lin, Y.2
  • 18
    • 85065137145 scopus 로고
    • (a) A review on the Ullmann reaction: Fanta, P. E. Synthesis 1974, 9-21.
    • (1974) Synthesis , pp. 9-21
    • Fanta, P.E.1
  • 19
    • 0001177138 scopus 로고
    • Other examples of the Ullmann reaction: (a) Lindsten, G.; Wennerstrom, O.; Isaksson, R. J. Org. Chem. 1987, 52, 547-554. (b) Matsumoto, H.; Inaba, S.; Rieke, R. D. J. Org. Chem. 1983, 48, 840-843. (c) Tsou, T. T.; Kochi, J. K. J. Am. Chem. Soc. 1979, 101, 7547-7560. (d) Takagi, K.; Hayama, M.; Inokawa, S. Chem. Lett. 1979, 917-918. (e) Bamfield, P.; Quan, P. M. Synthesis 1978, 537-538.
    • (1987) J. Org. Chem. , vol.52 , pp. 547-554
    • Lindsten, G.1    Wennerstrom, O.2    Isaksson, R.3
  • 20
    • 33845550516 scopus 로고
    • Other examples of the Ullmann reaction: (a) Lindsten, G.; Wennerstrom, O.; Isaksson, R. J. Org. Chem. 1987, 52, 547-554. (b) Matsumoto, H.; Inaba, S.; Rieke, R. D. J. Org. Chem. 1983, 48, 840-843. (c) Tsou, T. T.; Kochi, J. K. J. Am. Chem. Soc. 1979, 101, 7547-7560. (d) Takagi, K.; Hayama, M.; Inokawa, S. Chem. Lett. 1979, 917-918. (e) Bamfield, P.; Quan, P. M. Synthesis 1978, 537-538.
    • (1983) J. Org. Chem. , vol.48 , pp. 840-843
    • Matsumoto, H.1    Inaba, S.2    Rieke, R.D.3
  • 21
    • 0000277784 scopus 로고
    • Other examples of the Ullmann reaction: (a) Lindsten, G.; Wennerstrom, O.; Isaksson, R. J. Org. Chem. 1987, 52, 547-554. (b) Matsumoto, H.; Inaba, S.; Rieke, R. D. J. Org. Chem. 1983, 48, 840-843. (c) Tsou, T. T.; Kochi, J. K. J. Am. Chem. Soc. 1979, 101, 7547-7560. (d) Takagi, K.; Hayama, M.; Inokawa, S. Chem. Lett. 1979, 917-918. (e) Bamfield, P.; Quan, P. M. Synthesis 1978, 537-538.
    • (1979) J. Am. Chem. Soc. , vol.101 , pp. 7547-7560
    • Tsou, T.T.1    Kochi, J.K.2
  • 22
    • 0002754026 scopus 로고
    • Other examples of the Ullmann reaction: (a) Lindsten, G.; Wennerstrom, O.; Isaksson, R. J. Org. Chem. 1987, 52, 547-554. (b) Matsumoto, H.; Inaba, S.; Rieke, R. D. J. Org. Chem. 1983, 48, 840-843. (c) Tsou, T. T.; Kochi, J. K. J. Am. Chem. Soc. 1979, 101, 7547-7560. (d) Takagi, K.; Hayama, M.; Inokawa, S. Chem. Lett. 1979, 917-918. (e) Bamfield, P.; Quan, P. M. Synthesis 1978, 537-538.
    • (1979) Chem. Lett. , pp. 917-918
    • Takagi, K.1    Hayama, M.2    Inokawa, S.3
  • 23
    • 85024471340 scopus 로고
    • Other examples of the Ullmann reaction: (a) Lindsten, G.; Wennerstrom, O.; Isaksson, R. J. Org. Chem. 1987, 52, 547-554. (b) Matsumoto, H.; Inaba, S.; Rieke, R. D. J. Org. Chem. 1983, 48, 840-843. (c) Tsou, T. T.; Kochi, J. K. J. Am. Chem. Soc. 1979, 101, 7547-7560. (d) Takagi, K.; Hayama, M.; Inokawa, S. Chem. Lett. 1979, 917-918. (e) Bamfield, P.; Quan, P. M. Synthesis 1978, 537-538.
    • (1978) Synthesis , pp. 537-538
    • Bamfield, P.1    Quan, P.M.2
  • 24
    • 84942183942 scopus 로고
    • A very recent diaryl synthesis through Suzuki methodology: (a) Anderson J. C.; Namli, H. Synlett 1995, 765-766. Other papers on Suzuki reaction: (b) Watanabe, T.; Miyaura, N.; Suzuki, A. Synlett 1992, 207-210. (c) Suzuki, A. Pure Appl. Chem. 1994, 213-222.
    • (1995) Synlett , pp. 765-766
    • Anderson, J.C.1    Namli, H.2
  • 25
    • 85039397112 scopus 로고
    • A very recent diaryl synthesis through Suzuki methodology: (a) Anderson J. C.; Namli, H. Synlett 1995, 765-766. Other papers on Suzuki reaction: (b) Watanabe, T.; Miyaura, N.; Suzuki, A. Synlett 1992, 207-210. (c) Suzuki, A. Pure Appl. Chem. 1994, 213-222.
    • (1992) Synlett , pp. 207-210
    • Watanabe, T.1    Miyaura, N.2    Suzuki, A.3
  • 26
    • 0009686815 scopus 로고
    • A very recent diaryl synthesis through Suzuki methodology: (a) Anderson J. C.; Namli, H. Synlett 1995, 765-766. Other papers on Suzuki reaction: (b) Watanabe, T.; Miyaura, N.; Suzuki, A. Synlett 1992, 207-210. (c) Suzuki, A. Pure Appl. Chem. 1994, 213-222.
    • (1994) Pure Appl. Chem. , pp. 213-222
    • Suzuki, A.1
  • 27
    • 70349775545 scopus 로고
    • (a) Raju, G. V.; Rao, K. S. Curr. Sci. 1987, 56, 1280-1281; Chem. Abstr. 1988, 109; 128873y.
    • (1987) Curr. Sci. , vol.56 , pp. 1280-1281
    • Raju, G.V.1    Rao, K.S.2
  • 28
    • 85033810953 scopus 로고
    • (a) Raju, G. V.; Rao, K. S. Curr. Sci. 1987, 56, 1280-1281; Chem. Abstr. 1988, 109; 128873y.
    • (1988) Chem. Abstr. , vol.109
  • 30
    • 51249169200 scopus 로고
    • (b) Rao, V. K.; Ghary, T. J.; Murthy, A. K. Proc. Indian Acad. Sci., Chem. Sci. 1992, 104, 569-576; Chem. Abstr. 1993, 118, 6902x.
    • (1993) Chem. Abstr. , vol.118
  • 32
    • 0004198491 scopus 로고
    • Wiley-Interscience: New York
    • (a) Ho, T.-L. Tandem Organic Reactions; Wiley-Interscience: New York, 1992; pp 288.
    • (1992) Tandem Organic Reactions , pp. 288
    • Ho, T.-L.1
  • 36
    • 85033812065 scopus 로고    scopus 로고
    • Eur. Pat. Appl. EP 476.760, 1992
    • (a) Welter, T. R.; Delany, J. J. Eur. Pat. Appl. EP 476.760, 1992.
    • Welter, T.R.1    Delany, J.J.2
  • 43
    • 3643138899 scopus 로고
    • (a) Tomita, K.; Mizugai, M. Jpn. Kokai 1979, 7952074; Chem. Abstr. 1980, 92, 41921.
    • (1980) Chem. Abstr. , vol.92 , pp. 41921
  • 44
    • 3643059660 scopus 로고
    • (b) Hong, S. J. Kwajak. Konghak. 1973, 11, 404; Chem. Abstr. 1974, 81; 7293.
    • (1973) Kwajak. Konghak. , vol.11 , pp. 404
    • Hong, S.J.1
  • 45
    • 3643077467 scopus 로고
    • (b) Hong, S. J. Kwajak. Konghak. 1973, 11, 404; Chem. Abstr. 1974, 81; 7293.
    • (1974) Chem. Abstr. , vol.81 , pp. 7293
  • 48
    • 3643125357 scopus 로고
    • (b) 1983, 413-414;
    • (1983) Synthesis , pp. 413-414
  • 49
    • 3643054417 scopus 로고
    • (c) 1984, 510-512.
    • (1984) Synthesis , pp. 510-512
  • 70
    • 17444413314 scopus 로고
    • For some uses of DIBAL-H see: (a) Carreño, M. C.; García-Ruano, J. L.; Garrido, M.; Ruiz, H. P.; Solladié, G. Tetrahedron Lett. 1990, 31, 6653-6656. (b) Alexakis, A.; Duffault, J. M. Tetrahedron Lett. 1988, 29, 6243-6246.
    • (1988) Tetrahedron Lett. , vol.29 , pp. 6243-6246
    • Alexakis, A.1    Duffault, J.M.2
  • 75
    • 85033827915 scopus 로고    scopus 로고
    • note
    • Similarly to some other isoxazolium salts of the literature (see ref 23), 6a turned yellow and decomposed in 1-2 months at room temperature.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.