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Volumn 63, Issue 9, 1998, Pages 2858-2866

Detailed Characterization of p-Toluenesulfonic Acid Monohydrate as a Convenient, Recoverable, Safe, and Selective Catalyst for Alkylation of the Aromatic Nucleus

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EID: 0001759458     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo971832r     Document Type: Article
Times cited : (49)

References (74)
  • 3
    • 0009349575 scopus 로고
    • Friedel, C.; Crafts, J. M. Compt. Rend. 1877, 84, 1392, 1450. Friedel, C.; Crafts, J. M. Compt. Rend. 1877, 85, 74.
    • (1877) Compt. Rend. , vol.84 , pp. 1392
    • Friedel, C.1    Crafts, J.M.2
  • 4
    • 0346511669 scopus 로고
    • Friedel, C.; Crafts, J. M. Compt. Rend. 1877, 84, 1392, 1450. Friedel, C.; Crafts, J. M. Compt. Rend. 1877, 85, 74.
    • (1877) Compt. Rend. , vol.85 , pp. 74
    • Friedel, C.1    Crafts, J.M.2
  • 5
    • 0003492898 scopus 로고
    • Wiley: New York
    • For review see: (a) Friedel-Crafts and Related Reactions; Olah, G. A., Ed.; Wiley: New York, 1963-64; Vol. I-IV. (b) Olah, G. A. Friedel-Crafts Chemistry; Wiley-Interscience: New York, 1973. (c) Olah, G. A.; Krishnamurti, R.; Prakash, G. K. S. In Comprehensive Organic Synthesis; Trost, B. M., Fleming, I., Eds.; Pergamon Press: New York, 1991; Vol. 3, pp 293-339.
    • (1963) Friedel-Crafts and Related Reactions , vol.1-4
    • Olah, G.A.1
  • 6
    • 0003778227 scopus 로고
    • Wiley-Interscience: New York
    • For review see: (a) Friedel-Crafts and Related Reactions; Olah, G. A., Ed.; Wiley: New York, 1963-64; Vol. I-IV. (b) Olah, G. A. Friedel-Crafts Chemistry; Wiley-Interscience: New York, 1973. (c) Olah, G. A.; Krishnamurti, R.; Prakash, G. K. S. In Comprehensive Organic Synthesis; Trost, B. M., Fleming, I., Eds.; Pergamon Press: New York, 1991; Vol. 3, pp 293-339.
    • (1973) Friedel-Crafts Chemistry
    • Olah, G.A.1
  • 7
    • 0001586671 scopus 로고
    • Trost, B. M., Fleming, I., Eds.; Pergamon Press: New York
    • For review see: (a) Friedel-Crafts and Related Reactions; Olah, G. A., Ed.; Wiley: New York, 1963-64; Vol. I-IV. (b) Olah, G. A. Friedel-Crafts Chemistry; Wiley-Interscience: New York, 1973. (c) Olah, G. A.; Krishnamurti, R.; Prakash, G. K. S. In Comprehensive Organic Synthesis; Trost, B. M., Fleming, I., Eds.; Pergamon Press: New York, 1991; Vol. 3, pp 293-339.
    • (1991) Comprehensive Organic Synthesis , vol.3 , pp. 293-339
    • Olah, G.A.1    Krishnamurti, R.2    Prakash, G.K.S.3
  • 8
    • 0345894980 scopus 로고
    • Bowlus, H.; Nieuwland, J. J. Am. Chem. Soc. 1931, 53, 3835. Meerwein, H.; Pannwitz, W. J. Prakt. Chem. 1934, 141, 123. Booth, H. S.; Martin, D. R. Boron Trifluoride and Its Derivatives; Wiley: New York, 1949. Topchiev, A. V.; Zavgorodnii, S. V.; Paushkin, Y. M. Boron Trifluoride and Its Compounds as Catalysts in Organic Chemistry (Eng. Ed.); Pergamon Press: New York, 1959.
    • (1931) J. Am. Chem. Soc. , vol.53 , pp. 3835
    • Bowlus, H.1    Nieuwland, J.2
  • 9
    • 0346376955 scopus 로고
    • Bowlus, H.; Nieuwland, J. J. Am. Chem. Soc. 1931, 53, 3835. Meerwein, H.; Pannwitz, W. J. Prakt. Chem. 1934, 141, 123. Booth, H. S.; Martin, D. R. Boron Trifluoride and Its Derivatives; Wiley: New York, 1949. Topchiev, A. V.; Zavgorodnii, S. V.; Paushkin, Y. M. Boron Trifluoride and Its Compounds as Catalysts in Organic Chemistry (Eng. Ed.); Pergamon Press: New York, 1959.
    • (1934) J. Prakt. Chem. , vol.141 , pp. 123
    • Meerwein, H.1    Pannwitz, W.2
  • 10
    • 0004015385 scopus 로고
    • Wiley: New York
    • Bowlus, H.; Nieuwland, J. J. Am. Chem. Soc. 1931, 53, 3835. Meerwein, H.; Pannwitz, W. J. Prakt. Chem. 1934, 141, 123. Booth, H. S.; Martin, D. R. Boron Trifluoride and Its Derivatives; Wiley: New York, 1949. Topchiev, A. V.; Zavgorodnii, S. V.; Paushkin, Y. M. Boron Trifluoride and Its Compounds as Catalysts in Organic Chemistry (Eng. Ed.); Pergamon Press: New York, 1959.
    • (1949) Boron Trifluoride and Its Derivatives
    • Booth, H.S.1    Martin, D.R.2
  • 12
    • 37049066674 scopus 로고
    • Larock, R. C.; Johnson, P. L. J. Chem. Soc., Chem. Commun. 1989, 1368. Holland, H. L.; Kindermann, M.; Kumaresan, S.; Stefanac, T. Tetrahedron: Asymmetry 1993, 4, 1353. Olah, G. A.; Lee, C. S.; Prakash, G. K. S. J. Org. Chem. 1994, 59, 2590.
    • (1989) J. Chem. Soc., Chem. Commun. , pp. 1368
    • Larock, R.C.1    Johnson, P.L.2
  • 14
    • 0008895316 scopus 로고
    • Larock, R. C.; Johnson, P. L. J. Chem. Soc., Chem. Commun. 1989, 1368. Holland, H. L.; Kindermann, M.; Kumaresan, S.; Stefanac, T. Tetrahedron: Asymmetry 1993, 4, 1353. Olah, G. A.; Lee, C. S.; Prakash, G. K. S. J. Org. Chem. 1994, 59, 2590.
    • (1994) J. Org. Chem. , vol.59 , pp. 2590
    • Olah, G.A.1    Lee, C.S.2    Prakash, G.K.S.3
  • 15
    • 0001606689 scopus 로고
    • Lipshutz, B. H.; Wilhelm, R. S.; Kozlowski, J. A. Tetrahedron 1984, 40, 5005. Corey, E. J.; Posner, G. H. J. Am. Chem. Soc. 1967, 89, 3911. Brunner, H.; Kramler, K. Synthesis 1991, 1121. Fujiwara, Y.; Moritani, I.; Danno, S. J. Am. Chem. Soc. 1969, 91, 7166. Danno, S.; Moritani, I.; Fujiwara, Y. Tetrahedron 1969, 25, 4809. Heck, R. F. J. Am. Chem. Soc. 1968, 90, 5518. Heck, R. F. J. Am. Chem. Soc. 1969, 91, 6707. Garves, K. J. Org. Chem. 1970, 35, 3273. Horino, H.; Inoue, N. Bull. Chem. Soc. Jpn. 1971, 44, 3210. Horino, H.; Arai, M.; Inoue, N. Tetrahedron Lett. 1974, 647. Catellani, M.; Chiusoli, G. P. J. Organomet. Chem. 1988, 346, C27.
    • (1984) Tetrahedron , vol.40 , pp. 5005
    • Lipshutz, B.H.1    Wilhelm, R.S.2    Kozlowski, J.A.3
  • 16
    • 0009296615 scopus 로고
    • Lipshutz, B. H.; Wilhelm, R. S.; Kozlowski, J. A. Tetrahedron 1984, 40, 5005. Corey, E. J.; Posner, G. H. J. Am. Chem. Soc. 1967, 89, 3911. Brunner, H.; Kramler, K. Synthesis 1991, 1121. Fujiwara, Y.; Moritani, I.; Danno, S. J. Am. Chem. Soc. 1969, 91, 7166. Danno, S.; Moritani, I.; Fujiwara, Y. Tetrahedron 1969, 25, 4809. Heck, R. F. J. Am. Chem. Soc. 1968, 90, 5518. Heck, R. F. J. Am. Chem. Soc. 1969, 91, 6707. Garves, K. J. Org. Chem. 1970, 35, 3273. Horino, H.; Inoue, N. Bull. Chem. Soc. Jpn. 1971, 44, 3210. Horino, H.; Arai, M.; Inoue, N. Tetrahedron Lett. 1974, 647. Catellani, M.; Chiusoli, G. P. J. Organomet. Chem. 1988, 346, C27.
    • (1967) J. Am. Chem. Soc. , vol.89 , pp. 3911
    • Corey, E.J.1    Posner, G.H.2
  • 17
    • 0026351422 scopus 로고
    • Lipshutz, B. H.; Wilhelm, R. S.; Kozlowski, J. A. Tetrahedron 1984, 40, 5005. Corey, E. J.; Posner, G. H. J. Am. Chem. Soc. 1967, 89, 3911. Brunner, H.; Kramler, K. Synthesis 1991, 1121. Fujiwara, Y.; Moritani, I.; Danno, S. J. Am. Chem. Soc. 1969, 91, 7166. Danno, S.; Moritani, I.; Fujiwara, Y. Tetrahedron 1969, 25, 4809. Heck, R. F. J. Am. Chem. Soc. 1968, 90, 5518. Heck, R. F. J. Am. Chem. Soc. 1969, 91, 6707. Garves, K. J. Org. Chem. 1970, 35, 3273. Horino, H.; Inoue, N. Bull. Chem. Soc. Jpn. 1971, 44, 3210. Horino, H.; Arai, M.; Inoue, N. Tetrahedron Lett. 1974, 647. Catellani, M.; Chiusoli, G. P. J. Organomet. Chem. 1988, 346, C27.
    • (1991) Synthesis , pp. 1121
    • Brunner, H.1    Kramler, K.2
  • 18
    • 0000875742 scopus 로고
    • Lipshutz, B. H.; Wilhelm, R. S.; Kozlowski, J. A. Tetrahedron 1984, 40, 5005. Corey, E. J.; Posner, G. H. J. Am. Chem. Soc. 1967, 89, 3911. Brunner, H.; Kramler, K. Synthesis 1991, 1121. Fujiwara, Y.; Moritani, I.; Danno, S. J. Am. Chem. Soc. 1969, 91, 7166. Danno, S.; Moritani, I.; Fujiwara, Y. Tetrahedron 1969, 25, 4809. Heck, R. F. J. Am. Chem. Soc. 1968, 90, 5518. Heck, R. F. J. Am. Chem. Soc. 1969, 91, 6707. Garves, K. J. Org. Chem. 1970, 35, 3273. Horino, H.; Inoue, N. Bull. Chem. Soc. Jpn. 1971, 44, 3210. Horino, H.; Arai, M.; Inoue, N. Tetrahedron Lett. 1974, 647. Catellani, M.; Chiusoli, G. P. J. Organomet. Chem. 1988, 346, C27.
    • (1969) J. Am. Chem. Soc. , vol.91 , pp. 7166
    • Fujiwara, Y.1    Moritani, I.2    Danno, S.3
  • 19
    • 0141678757 scopus 로고
    • Lipshutz, B. H.; Wilhelm, R. S.; Kozlowski, J. A. Tetrahedron 1984, 40, 5005. Corey, E. J.; Posner, G. H. J. Am. Chem. Soc. 1967, 89, 3911. Brunner, H.; Kramler, K. Synthesis 1991, 1121. Fujiwara, Y.; Moritani, I.; Danno, S. J. Am. Chem. Soc. 1969, 91, 7166. Danno, S.; Moritani, I.; Fujiwara, Y. Tetrahedron 1969, 25, 4809. Heck, R. F. J. Am. Chem. Soc. 1968, 90, 5518. Heck, R. F. J. Am. Chem. Soc. 1969, 91, 6707. Garves, K. J. Org. Chem. 1970, 35, 3273. Horino, H.; Inoue, N. Bull. Chem. Soc. Jpn. 1971, 44, 3210. Horino, H.; Arai, M.; Inoue, N. Tetrahedron Lett. 1974, 647. Catellani, M.; Chiusoli, G. P. J. Organomet. Chem. 1988, 346, C27.
    • (1969) Tetrahedron , vol.25 , pp. 4809
    • Danno, S.1    Moritani, I.2    Fujiwara, Y.3
  • 20
    • 13044307437 scopus 로고
    • Lipshutz, B. H.; Wilhelm, R. S.; Kozlowski, J. A. Tetrahedron 1984, 40, 5005. Corey, E. J.; Posner, G. H. J. Am. Chem. Soc. 1967, 89, 3911. Brunner, H.; Kramler, K. Synthesis 1991, 1121. Fujiwara, Y.; Moritani, I.; Danno, S. J. Am. Chem. Soc. 1969, 91, 7166. Danno, S.; Moritani, I.; Fujiwara, Y. Tetrahedron 1969, 25, 4809. Heck, R. F. J. Am. Chem. Soc. 1968, 90, 5518. Heck, R. F. J. Am. Chem. Soc. 1969, 91, 6707. Garves, K. J. Org. Chem. 1970, 35, 3273. Horino, H.; Inoue, N. Bull. Chem. Soc. Jpn. 1971, 44, 3210. Horino, H.; Arai, M.; Inoue, N. Tetrahedron Lett. 1974, 647. Catellani, M.; Chiusoli, G. P. J. Organomet. Chem. 1988, 346, C27.
    • (1968) J. Am. Chem. Soc. , vol.90 , pp. 5518
    • Heck, R.F.1
  • 21
    • 33947299933 scopus 로고
    • Lipshutz, B. H.; Wilhelm, R. S.; Kozlowski, J. A. Tetrahedron 1984, 40, 5005. Corey, E. J.; Posner, G. H. J. Am. Chem. Soc. 1967, 89, 3911. Brunner, H.; Kramler, K. Synthesis 1991, 1121. Fujiwara, Y.; Moritani, I.; Danno, S. J. Am. Chem. Soc. 1969, 91, 7166. Danno, S.; Moritani, I.; Fujiwara, Y. Tetrahedron 1969, 25, 4809. Heck, R. F. J. Am. Chem. Soc. 1968, 90, 5518. Heck, R. F. J. Am. Chem. Soc. 1969, 91, 6707. Garves, K. J. Org. Chem. 1970, 35, 3273. Horino, H.; Inoue, N. Bull. Chem. Soc. Jpn. 1971, 44, 3210. Horino, H.; Arai, M.; Inoue, N. Tetrahedron Lett. 1974, 647. Catellani, M.; Chiusoli, G. P. J. Organomet. Chem. 1988, 346, C27.
    • (1969) J. Am. Chem. Soc. , vol.91 , pp. 6707
    • Heck, R.F.1
  • 22
    • 0005115325 scopus 로고
    • Lipshutz, B. H.; Wilhelm, R. S.; Kozlowski, J. A. Tetrahedron 1984, 40, 5005. Corey, E. J.; Posner, G. H. J. Am. Chem. Soc. 1967, 89, 3911. Brunner, H.; Kramler, K. Synthesis 1991, 1121. Fujiwara, Y.; Moritani, I.; Danno, S. J. Am. Chem. Soc. 1969, 91, 7166. Danno, S.; Moritani, I.; Fujiwara, Y. Tetrahedron 1969, 25, 4809. Heck, R. F. J. Am. Chem. Soc. 1968, 90, 5518. Heck, R. F. J. Am. Chem. Soc. 1969, 91, 6707. Garves, K. J. Org. Chem. 1970, 35, 3273. Horino, H.; Inoue, N. Bull. Chem. Soc. Jpn. 1971, 44, 3210. Horino, H.; Arai, M.; Inoue, N. Tetrahedron Lett. 1974, 647. Catellani, M.; Chiusoli, G. P. J. Organomet. Chem. 1988, 346, C27.
    • (1970) J. Org. Chem. , vol.35 , pp. 3273
    • Garves, K.1
  • 23
    • 1542714366 scopus 로고
    • Lipshutz, B. H.; Wilhelm, R. S.; Kozlowski, J. A. Tetrahedron 1984, 40, 5005. Corey, E. J.; Posner, G. H. J. Am. Chem. Soc. 1967, 89, 3911. Brunner, H.; Kramler, K. Synthesis 1991, 1121. Fujiwara, Y.; Moritani, I.; Danno, S. J. Am. Chem. Soc. 1969, 91, 7166. Danno, S.; Moritani, I.; Fujiwara, Y. Tetrahedron 1969, 25, 4809. Heck, R. F. J. Am. Chem. Soc. 1968, 90, 5518. Heck, R. F. J. Am. Chem. Soc. 1969, 91, 6707. Garves, K. J. Org. Chem. 1970, 35, 3273. Horino, H.; Inoue, N. Bull. Chem. Soc. Jpn. 1971, 44, 3210. Horino, H.; Arai, M.; Inoue, N. Tetrahedron Lett. 1974, 647. Catellani, M.; Chiusoli, G. P. J. Organomet. Chem. 1988, 346, C27.
    • (1971) Bull. Chem. Soc. Jpn. , vol.44 , pp. 3210
    • Horino, H.1    Inoue, N.2
  • 24
    • 0001940158 scopus 로고
    • Lipshutz, B. H.; Wilhelm, R. S.; Kozlowski, J. A. Tetrahedron 1984, 40, 5005. Corey, E. J.; Posner, G. H. J. Am. Chem. Soc. 1967, 89, 3911. Brunner, H.; Kramler, K. Synthesis 1991, 1121. Fujiwara, Y.; Moritani, I.; Danno, S. J. Am. Chem. Soc. 1969, 91, 7166. Danno, S.; Moritani, I.; Fujiwara, Y. Tetrahedron 1969, 25, 4809. Heck, R. F. J. Am. Chem. Soc. 1968, 90, 5518. Heck, R. F. J. Am. Chem. Soc. 1969, 91, 6707. Garves, K. J. Org. Chem. 1970, 35, 3273. Horino, H.; Inoue, N. Bull. Chem. Soc. Jpn. 1971, 44, 3210. Horino, H.; Arai, M.; Inoue, N. Tetrahedron Lett. 1974, 647. Catellani, M.; Chiusoli, G. P. J. Organomet. Chem. 1988, 346, C27.
    • (1974) Tetrahedron Lett. , pp. 647
    • Horino, H.1    Arai, M.2    Inoue, N.3
  • 25
    • 0002406804 scopus 로고
    • Lipshutz, B. H.; Wilhelm, R. S.; Kozlowski, J. A. Tetrahedron 1984, 40, 5005. Corey, E. J.; Posner, G. H. J. Am. Chem. Soc. 1967, 89, 3911. Brunner, H.; Kramler, K. Synthesis 1991, 1121. Fujiwara, Y.; Moritani, I.; Danno, S. J. Am. Chem. Soc. 1969, 91, 7166. Danno, S.; Moritani, I.; Fujiwara, Y. Tetrahedron 1969, 25, 4809. Heck, R. F. J. Am. Chem. Soc. 1968, 90, 5518. Heck, R. F. J. Am. Chem. Soc. 1969, 91, 6707. Garves, K. J. Org. Chem. 1970, 35, 3273. Horino, H.; Inoue, N. Bull. Chem. Soc. Jpn. 1971, 44, 3210. Horino, H.; Arai, M.; Inoue, N. Tetrahedron Lett. 1974, 647. Catellani, M.; Chiusoli, G. P. J. Organomet. Chem. 1988, 346, C27.
    • (1988) Organomet. Chem. , vol.346
    • Catellani, M.1    Chiusoli, G.P.J.2
  • 26
    • 1542399753 scopus 로고    scopus 로고
    • in ref 4a, 1963; Vol. I, Chapter 4, pp 201-366
    • Olah, G. A., in ref 4a, 1963; Vol. I, Chapter 4, pp 201-366.
    • Olah, G.A.1
  • 28
    • 1542504783 scopus 로고    scopus 로고
    • Can. Patent 1,152,111, 1983
    • (b) Olah, G. A. Can. Patent 1,152,111, 1983; Chem. Abstr. 1984, 100, 34291.
    • Olah, G.A.1
  • 29
    • 1542504786 scopus 로고
    • (b) Olah, G. A. Can. Patent 1,152,111, 1983; Chem. Abstr. 1984, 100, 34291.
    • (1984) Chem. Abstr. , vol.100 , pp. 34291
  • 32
    • 1542504785 scopus 로고
    • U. S. Patent 2,014,766
    • (e) Isham, R. M. U. S. Patent 2,014,766, 1935; Chem. Abstr. 1935, 29, 7346.
    • (1935)
    • Isham, R.M.1
  • 33
    • 1542399765 scopus 로고
    • (e) Isham, R. M. U. S. Patent 2,014,766, 1935; Chem. Abstr. 1935, 29, 7346.
    • (1935) Chem. Abstr. , vol.29 , pp. 7346
  • 35
    • 1542399747 scopus 로고    scopus 로고
    • U.S. Patent 4,255,343, 1981
    • (g) Gosser, L. W. U.S. Patent 4,255,343, 1981; Chem. Abstr. 1981, 95, 42763.
    • Gosser, L.W.1
  • 36
    • 1542504769 scopus 로고
    • (g) Gosser, L. W. U.S. Patent 4,255,343, 1981; Chem. Abstr. 1981, 95, 42763.
    • (1981) Chem. Abstr. , vol.95 , pp. 42763
  • 37
    • 1542399740 scopus 로고    scopus 로고
    • U.S. Patent 2,462,792, 1949
    • (h) Wodsworth, F. T.; Lee, R. J. U.S. Patent 2,462,792, 1949; Chem. Abstr. 1949, 43, 4458.
    • Wodsworth, F.T.1    Lee, R.J.2
  • 38
    • 1542714377 scopus 로고
    • (h) Wodsworth, F. T.; Lee, R. J. U.S. Patent 2,462,792, 1949; Chem. Abstr. 1949, 43, 4458.
    • (1949) Chem. Abstr. , vol.43 , pp. 4458
  • 45
    • 1542714374 scopus 로고    scopus 로고
    • In ref 4a, 1963; Vol. I, Chapter 2, pp 25-168
    • Olah, G. A. In ref 4a, 1963; Vol. I, Chapter 2, pp 25-168.
    • Olah, G.A.1
  • 48
    • 1542399752 scopus 로고    scopus 로고
    • In ref 4a, 1964; Vol. II, Chapter 15, pp 289-412
    • Koncos, R.; Friedman, B. S. In ref 4a, 1964; Vol. II, Chapter 15, pp 289-412.
    • Koncos, R.1    Friedman, B.S.2
  • 49
    • 0001729278 scopus 로고
    • Raunio, E. K.; Bonner, W. A. J. Org. Chem. 1966, 31, 396. Rondestvedt, C. S., Jr. J. Am. Chem. Soc. 1951, 73, 4509 and references therein.
    • (1966) J. Org. Chem. , vol.31 , pp. 396
    • Raunio, E.K.1    Bonner, W.A.2
  • 50
    • 0742327261 scopus 로고
    • and references therein
    • Raunio, E. K.; Bonner, W. A. J. Org. Chem. 1966, 31, 396. Rondestvedt, C. S., Jr. J. Am. Chem. Soc. 1951, 73, 4509 and references therein.
    • (1951) J. Am. Chem. Soc. , vol.73 , pp. 4509
    • Rondestvedt Jr., C.S.1
  • 51
    • 1542504772 scopus 로고    scopus 로고
    • In ref 4a, 1964; Vol. II, Chapter 14, pp 1-288
    • Patinkin, S. H.; Friedman, B. S. In ref 4a, 1964; Vol. II, Chapter 14, pp 1-288.
    • Patinkin, S.H.1    Friedman, B.S.2
  • 54
    • 85162719929 scopus 로고
    • Kraemer, G.; Spilker, A.; Eberhardt, P. Ber. 1890, 23, 3269. Spilker, A.; Schade, W. Ber. 1932, 65B, 1686.
    • (1932) Ber. , vol.65 B , pp. 1686
    • Spilker, A.1    Schade, W.2
  • 55
    • 85088258945 scopus 로고    scopus 로고
    • note
    • 13C NMR analysis unequivocally confirmed the structure of 22-p which is identical to the product obtained from the tosylate 21 (entry 12, Table 1).
  • 58
    • 1542504773 scopus 로고
    • Pines, H.; Edeleanu, A.; Ipatieff, V. N. J. Am. Chem. Soc. 1945, 67, 2193. Friess, S. L.; Pinson, R., Jr. J. Am. Chem. Soc. 1951, 73, 3512.
    • (1951) J. Am. Chem. Soc. , vol.73 , pp. 3512
    • Friess, S.L.1    Pinson Jr., R.2
  • 61
    • 1542399746 scopus 로고    scopus 로고
    • In ref 4a, 1963; Vol. I, Chapter 13, pp 999-1015
    • Hart, H. In ref 4a, 1963; Vol. I, Chapter 13, pp 999-1015.
    • Hart, H.1
  • 63
    • 1542609340 scopus 로고    scopus 로고
    • However, generation of a carbenium ion intermediate from type A alkyl substrates could not be easily envisioned
    • However, generation of a carbenium ion intermediate from type A alkyl substrates could not be easily envisioned.
  • 68
    • 0642298307 scopus 로고
    • Olah, G. A., Schleyer, P. v. R., Eds.; John Wiley-Interscience: New York, Chapter 1
    • Nenitzescu, C. D. In Carbonium Ions; Olah, G. A., Schleyer, P. v. R., Eds.; John Wiley-Interscience: New York, 1968; Chapter 1, Vol. I, pp 1-75.
    • (1968) Carbonium Ions , vol.1 , pp. 1-75
    • Nenitzescu, C.D.1
  • 70
    • 1542399751 scopus 로고    scopus 로고
    • note
    • In this reaction, benzene was used instead of toluene to avoid further complication of the product distribution due to the formation of ortho, meta, and para isomers of the products.
  • 72
    • 0022188437 scopus 로고
    • Imelik, B., Naccache, C., Coudurier, G., Taarit, Y. B., Vedrine, J. C., Eds.; Elsevier Science Publishers B.V.: Amsterdam, The Netherlands
    • Weitkamp, J.; Ernst, S. In Catalysis by Acids and Bases; Imelik, B., Naccache, C., Coudurier, G., Taarit, Y. B., Vedrine, J. C., Eds.; Elsevier Science Publishers B.V.: Amsterdam, The Netherlands, 1985; pp 419-426.
    • (1985) Catalysis by Acids and Bases , pp. 419-426
    • Weitkamp, J.1    Ernst, S.2
  • 73
    • 0022201219 scopus 로고    scopus 로고
    • In ref 31, 1985, pp 283-297
    • Guisnet, M. In ref 31, 1985, pp 283-297.
    • Guisnet, M.1
  • 74
    • 1542504777 scopus 로고    scopus 로고
    • This proposal is also consistent with the observation that 22-p is the only product from 21
    • This proposal is also consistent with the observation that 22-p is the only product from 21.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.