메뉴 건너뛰기




Volumn 33, Issue 12, 2004, Pages 1588-1589

One-pot synthesis of furo[3,2-c]oxepin-4-one derivatives by the CAN-mediated reaction of tert-butyl 2-(2-hydroxytetrahydrofuran-2-yl)acetates with alkenes

Author keywords

[No Author keywords available]

Indexed keywords

ACETIC ACID DERIVATIVE; ALKENE DERIVATIVE; AMMONIUM NITRATE; CERIUM; FURAN DERIVATIVE; LACTONE DERIVATIVE; OXEPINE DERIVATIVE;

EID: 14844333190     PISSN: 03667022     EISSN: None     Source Type: Journal    
DOI: 10.1246/cl.2004.1588     Document Type: Article
Times cited : (11)

References (30)
  • 1
    • 0030500338 scopus 로고    scopus 로고
    • K. Kobayashi, M. Mori, T. Uneda, O. Morikawa, and H. Konishi, Chem. Lett., 1996, 451; K. Kobayashi, T. Uneda, K. Tanaka, M. Mori, H. Tanaka, O. Morikawa, and H. Konishi, Bull. Chem. Soc. Jpn., 71, 1691 (1998); K. Kobayashi, K. Sakashita, H. Akamatsu, K. Tanaka, M. Uchida, T. Uneda, T. Kitamura, O. Morikawa, and H. Konishi, Heterocycles, 51, 2881 (1999); K. Kobayashi, H. Tanaka, K. Tanaka, K. Yoneda, O. Morikawa, and H. Konishi, Synth. Commun., 30, 4277 (2000); K. Kobayashi, K. Nagase, O. Morikawa, and H. Konishi, Heterocycles, 60, 939 (2003).
    • (1996) Chem. Lett. , pp. 451
    • Kobayashi, K.1    Mori, M.2    Uneda, T.3    Morikawa, O.4    Konishi, H.5
  • 2
    • 0001748898 scopus 로고    scopus 로고
    • K. Kobayashi, M. Mori, T. Uneda, O. Morikawa, and H. Konishi, Chem. Lett., 1996, 451; K. Kobayashi, T. Uneda, K. Tanaka, M. Mori, H. Tanaka, O. Morikawa, and H. Konishi, Bull. Chem. Soc. Jpn., 71, 1691 (1998); K. Kobayashi, K. Sakashita, H. Akamatsu, K. Tanaka, M. Uchida, T. Uneda, T. Kitamura, O. Morikawa, and H. Konishi, Heterocycles, 51, 2881 (1999); K. Kobayashi, H. Tanaka, K. Tanaka, K. Yoneda, O. Morikawa, and H. Konishi, Synth. Commun., 30, 4277 (2000); K. Kobayashi, K. Nagase, O. Morikawa, and H. Konishi, Heterocycles, 60, 939 (2003).
    • (1998) Bull. Chem. Soc. Jpn. , vol.71 , pp. 1691
    • Kobayashi, K.1    Uneda, T.2    Tanaka, K.3    Mori, M.4    Tanaka, H.5    Morikawa, O.6    Konishi, H.7
  • 3
    • 0033378053 scopus 로고    scopus 로고
    • K. Kobayashi, M. Mori, T. Uneda, O. Morikawa, and H. Konishi, Chem. Lett., 1996, 451; K. Kobayashi, T. Uneda, K. Tanaka, M. Mori, H. Tanaka, O. Morikawa, and H. Konishi, Bull. Chem. Soc. Jpn., 71, 1691 (1998); K. Kobayashi, K. Sakashita, H. Akamatsu, K. Tanaka, M. Uchida, T. Uneda, T. Kitamura, O. Morikawa, and H. Konishi, Heterocycles, 51, 2881 (1999); K. Kobayashi, H. Tanaka, K. Tanaka, K. Yoneda, O. Morikawa, and H. Konishi, Synth. Commun., 30, 4277 (2000); K. Kobayashi, K. Nagase, O. Morikawa, and H. Konishi, Heterocycles, 60, 939 (2003).
    • (1999) Heterocycles , vol.51 , pp. 2881
    • Kobayashi, K.1    Sakashita, K.2    Akamatsu, H.3    Tanaka, K.4    Uchida, M.5    Uneda, T.6    Kitamura, T.7    Morikawa, O.8    Konishi, H.9
  • 4
    • 0033786009 scopus 로고    scopus 로고
    • K. Kobayashi, M. Mori, T. Uneda, O. Morikawa, and H. Konishi, Chem. Lett., 1996, 451; K. Kobayashi, T. Uneda, K. Tanaka, M. Mori, H. Tanaka, O. Morikawa, and H. Konishi, Bull. Chem. Soc. Jpn., 71, 1691 (1998); K. Kobayashi, K. Sakashita, H. Akamatsu, K. Tanaka, M. Uchida, T. Uneda, T. Kitamura, O. Morikawa, and H. Konishi, Heterocycles, 51, 2881 (1999); K. Kobayashi, H. Tanaka, K. Tanaka, K. Yoneda, O. Morikawa, and H. Konishi, Synth. Commun., 30, 4277 (2000); K. Kobayashi, K. Nagase, O. Morikawa, and H. Konishi, Heterocycles, 60, 939 (2003).
    • (2000) Synth. Commun. , vol.30 , pp. 4277
    • Kobayashi, K.1    Tanaka, H.2    Tanaka, K.3    Yoneda, K.4    Morikawa, O.5    Konishi, H.6
  • 5
    • 0037388174 scopus 로고    scopus 로고
    • K. Kobayashi, M. Mori, T. Uneda, O. Morikawa, and H. Konishi, Chem. Lett., 1996, 451; K. Kobayashi, T. Uneda, K. Tanaka, M. Mori, H. Tanaka, O. Morikawa, and H. Konishi, Bull. Chem. Soc. Jpn., 71, 1691 (1998); K. Kobayashi, K. Sakashita, H. Akamatsu, K. Tanaka, M. Uchida, T. Uneda, T. Kitamura, O. Morikawa, and H. Konishi, Heterocycles, 51, 2881 (1999); K. Kobayashi, H. Tanaka, K. Tanaka, K. Yoneda, O. Morikawa, and H. Konishi, Synth. Commun., 30, 4277 (2000); K. Kobayashi, K. Nagase, O. Morikawa, and H. Konishi, Heterocycles, 60, 939 (2003).
    • (2003) Heterocycles , vol.60 , pp. 939
    • Kobayashi, K.1    Nagase, K.2    Morikawa, O.3    Konishi, H.4
  • 6
    • 14844321114 scopus 로고
    • ed. by W. J. Mijs and C. R. H. I. de Jonge, Plenum Press, New York Chapter 4
    • 3, have been used as a mediator for the cycloaddition reaction of 1,3-dicarbonyl and related compounds with alkenes forming 1,2-dihydrofuran derivatives. For earlier works: W. J. De Klein, "Organic Syntheses by Oxidation with Metal Compounds," ed. by W. J. Mijs and C. R. H. I. de Jonge, Plenum Press, New York (1986), Chapter 4; For recent reviews: V. Nair, J. Matthew, and J. Prabhakaran, Chem. Soc. Rev., 26, 127 (1997); J. Iqval and M. Mukhopadhyay, Synlett, 1997, 876; For more recent reports: Y. R. Lee, J. Y. Suk, and B. S. Kim, Org. Lett., 2, 1387 (2000); Y. R. Lee, B. S. Kim, and H. I. Kweon, Tetrahedron, 56, 3867 (2000); G. Bar, A. F. Parsons, and C. B. Thomas, Tetrahedron Lett., 41, 7751 (2000); Y. R. Lee, B. S. Kim, and D. H. Kim, Tetrahedron, 56, 8845 (2000); S. Kajiwara, H. Nishino, and K. Kurosawa, Heterocycles, 54, 171 (2001); Y. R. Lee and B. S. Kim, Synth. Commun., 31, 381 (2001); G. Bar, A. F. Parsons, and C. B. Thomas, Chem. Commun., 2001, 1350; M. Yilmaz and A. T. Pekel, Synth. Commun., 31, 2189 (2001); G. Bar, A. F. Parsons, and C. B. Thomas, Tetrahedron, 57, 4719 (2001); V. Nair, P. M. Treesa, D. Maliakal, and N. P. Rath, Tetrahedron, 57, 7705 (2001); S. Muthusamy, C. Gunanathan, and S. A. Babu, Synlett, 2002, 787; Y. R. Lee, B. S. Kim, Y. U. Yung, W. S. Koh, J. S. Cha, and N. W. Kim, Synth. Commun., 32, 3099 (2002); M. C. S. de-Mattos, S. P. L. de-Souza, and S. M. Elias, Heterocycl. Commun., 9, 247 (2003); Y. R. Lee, K. Y. Kang, G. J. Lee, and W. K. Lee, Synthesis, 2003, 1977; N. N. Karade, S. G. Shirodkar, M. N. Patil, R. A. Potrekar, and H. N. Karade, Tetrahedron Lett., 44, 6729 (2003); R. Kumabe and H. Nishino, Heterocycl. Commun., 10, 135 (2004); V. Jadhav, M. Y. Park, and Y. H. Kim, Synthesis, 2004, 329 and references cited therein.
    • (1986) Organic Syntheses by Oxidation with Metal Compounds
    • De Klein, W.J.1
  • 7
    • 33846307752 scopus 로고    scopus 로고
    • 3, have been used as a mediator for the cycloaddition reaction of 1,3-dicarbonyl and related compounds with alkenes forming 1,2-dihydrofuran derivatives. For earlier works: W. J. De Klein, "Organic Syntheses by Oxidation with Metal Compounds," ed. by W. J. Mijs and C. R. H. I. de Jonge, Plenum Press, New York (1986), Chapter 4; For recent reviews: V. Nair, J. Matthew, and J. Prabhakaran, Chem. Soc. Rev., 26, 127 (1997); J. Iqval and M. Mukhopadhyay, Synlett, 1997, 876; For more recent reports: Y. R. Lee, J. Y. Suk, and B. S. Kim, Org. Lett., 2, 1387 (2000); Y. R. Lee, B. S. Kim, and H. I. Kweon, Tetrahedron, 56, 3867 (2000); G. Bar, A. F. Parsons, and C. B. Thomas, Tetrahedron Lett., 41, 7751 (2000); Y. R. Lee, B. S. Kim, and D. H. Kim, Tetrahedron, 56, 8845 (2000); S. Kajiwara, H. Nishino, and K. Kurosawa, Heterocycles, 54, 171 (2001); Y. R. Lee and B. S. Kim, Synth. Commun., 31, 381 (2001); G. Bar, A. F. Parsons, and C. B. Thomas, Chem. Commun., 2001, 1350; M. Yilmaz and A. T. Pekel, Synth. Commun., 31, 2189 (2001); G. Bar, A. F. Parsons, and C. B. Thomas, Tetrahedron, 57, 4719 (2001); V. Nair, P. M. Treesa, D. Maliakal, and N. P. Rath, Tetrahedron, 57, 7705 (2001); S. Muthusamy, C. Gunanathan, and S. A. Babu, Synlett, 2002, 787; Y. R. Lee, B. S. Kim, Y. U. Yung, W. S. Koh, J. S. Cha, and N. W. Kim, Synth. Commun., 32, 3099 (2002); M. C. S. de-Mattos, S. P. L. de-Souza, and S. M. Elias, Heterocycl. Commun., 9, 247 (2003); Y. R. Lee, K. Y. Kang, G. J. Lee, and W. K. Lee, Synthesis, 2003, 1977; N. N. Karade, S. G. Shirodkar, M. N. Patil, R. A. Potrekar, and H. N. Karade, Tetrahedron Lett., 44, 6729 (2003); R. Kumabe and H. Nishino, Heterocycl. Commun., 10, 135 (2004); V. Jadhav, M. Y. Park, and Y. H. Kim, Synthesis, 2004, 329 and references cited therein.
    • (1997) Chem. Soc. Rev. , vol.26 , pp. 127
    • Nair, V.1    Matthew, J.2    Prabhakaran, J.3
  • 8
    • 0343819393 scopus 로고    scopus 로고
    • 3, have been used as a mediator for the cycloaddition reaction of 1,3-dicarbonyl and related compounds with alkenes forming 1,2-dihydrofuran derivatives. For earlier works: W. J. De Klein, "Organic Syntheses by Oxidation with Metal Compounds," ed. by W. J. Mijs and C. R. H. I. de Jonge, Plenum Press, New York (1986), Chapter 4; For recent reviews: V. Nair, J. Matthew, and J. Prabhakaran, Chem. Soc. Rev., 26, 127 (1997); J. Iqval and M. Mukhopadhyay, Synlett, 1997, 876; For more recent reports: Y. R. Lee, J. Y. Suk, and B. S. Kim, Org. Lett., 2, 1387 (2000); Y. R. Lee, B. S. Kim, and H. I. Kweon, Tetrahedron, 56, 3867 (2000); G. Bar, A. F. Parsons, and C. B. Thomas, Tetrahedron Lett., 41, 7751 (2000); Y. R. Lee, B. S. Kim, and D. H. Kim, Tetrahedron, 56, 8845 (2000); S. Kajiwara, H. Nishino, and K. Kurosawa, Heterocycles, 54, 171 (2001); Y. R. Lee and B. S. Kim, Synth. Commun., 31, 381 (2001); G. Bar, A. F. Parsons, and C. B. Thomas, Chem. Commun., 2001, 1350; M. Yilmaz and A. T. Pekel, Synth. Commun., 31, 2189 (2001); G. Bar, A. F. Parsons, and C. B. Thomas, Tetrahedron, 57, 4719 (2001); V. Nair, P. M. Treesa, D. Maliakal, and N. P. Rath, Tetrahedron, 57, 7705 (2001); S. Muthusamy, C. Gunanathan, and S. A. Babu, Synlett, 2002, 787; Y. R. Lee, B. S. Kim, Y. U. Yung, W. S. Koh, J. S. Cha, and N. W. Kim, Synth. Commun., 32, 3099 (2002); M. C. S. de-Mattos, S. P. L. de-Souza, and S. M. Elias, Heterocycl. Commun., 9, 247 (2003); Y. R. Lee, K. Y. Kang, G. J. Lee, and W. K. Lee, Synthesis, 2003, 1977; N. N. Karade, S. G. Shirodkar, M. N. Patil, R. A. Potrekar, and H. N. Karade, Tetrahedron Lett., 44, 6729 (2003); R. Kumabe and H. Nishino, Heterocycl. Commun., 10, 135 (2004); V. Jadhav, M. Y. Park, and Y. H. Kim, Synthesis, 2004, 329 and references cited therein.
    • (1997) Synlett , pp. 876
    • Iqval, J.1    Mukhopadhyay, M.2
  • 9
    • 0034682164 scopus 로고    scopus 로고
    • 3, have been used as a mediator for the cycloaddition reaction of 1,3-dicarbonyl and related compounds with alkenes forming 1,2-dihydrofuran derivatives. For earlier works: W. J. De Klein, "Organic Syntheses by Oxidation with Metal Compounds," ed. by W. J. Mijs and C. R. H. I. de Jonge, Plenum Press, New York (1986), Chapter 4; For recent reviews: V. Nair, J. Matthew, and J. Prabhakaran, Chem. Soc. Rev., 26, 127 (1997); J. Iqval and M. Mukhopadhyay, Synlett, 1997, 876; For more recent reports: Y. R. Lee, J. Y. Suk, and B. S. Kim, Org. Lett., 2, 1387 (2000); Y. R. Lee, B. S. Kim, and H. I. Kweon, Tetrahedron, 56, 3867 (2000); G. Bar, A. F. Parsons, and C. B. Thomas, Tetrahedron Lett., 41, 7751 (2000); Y. R. Lee, B. S. Kim, and D. H. Kim, Tetrahedron, 56, 8845 (2000); S. Kajiwara, H. Nishino, and K. Kurosawa, Heterocycles, 54, 171 (2001); Y. R. Lee and B. S. Kim, Synth. Commun., 31, 381 (2001); G. Bar, A. F. Parsons, and C. B. Thomas, Chem. Commun., 2001, 1350; M. Yilmaz and A. T. Pekel, Synth. Commun., 31, 2189 (2001); G. Bar, A. F. Parsons, and C. B. Thomas, Tetrahedron, 57, 4719 (2001); V. Nair, P. M. Treesa, D. Maliakal, and N. P. Rath, Tetrahedron, 57, 7705 (2001); S. Muthusamy, C. Gunanathan, and S. A. Babu, Synlett, 2002, 787; Y. R. Lee, B. S. Kim, Y. U. Yung, W. S. Koh, J. S. Cha, and N. W. Kim, Synth. Commun., 32, 3099 (2002); M. C. S. de-Mattos, S. P. L. de-Souza, and S. M. Elias, Heterocycl. Commun., 9, 247 (2003); Y. R. Lee, K. Y. Kang, G. J. Lee, and W. K. Lee, Synthesis, 2003, 1977; N. N. Karade, S. G. Shirodkar, M. N. Patil, R. A. Potrekar, and H. N. Karade, Tetrahedron Lett., 44, 6729 (2003); R. Kumabe and H. Nishino, Heterocycl. Commun., 10, 135 (2004); V. Jadhav, M. Y. Park, and Y. H. Kim, Synthesis, 2004, 329 and references cited therein.
    • (2000) Org. Lett. , vol.2 , pp. 1387
    • Lee, Y.R.1    Suk, J.Y.2    Kim, B.S.3
  • 10
    • 0343962195 scopus 로고    scopus 로고
    • 3, have been used as a mediator for the cycloaddition reaction of 1,3-dicarbonyl and related compounds with alkenes forming 1,2-dihydrofuran derivatives. For earlier works: W. J. De Klein, "Organic Syntheses by Oxidation with Metal Compounds," ed. by W. J. Mijs and C. R. H. I. de Jonge, Plenum Press, New York (1986), Chapter 4; For recent reviews: V. Nair, J. Matthew, and J. Prabhakaran, Chem. Soc. Rev., 26, 127 (1997); J. Iqval and M. Mukhopadhyay, Synlett, 1997, 876; For more recent reports: Y. R. Lee, J. Y. Suk, and B. S. Kim, Org. Lett., 2, 1387 (2000); Y. R. Lee, B. S. Kim, and H. I. Kweon, Tetrahedron, 56, 3867 (2000); G. Bar, A. F. Parsons, and C. B. Thomas, Tetrahedron Lett., 41, 7751 (2000); Y. R. Lee, B. S. Kim, and D. H. Kim, Tetrahedron, 56, 8845 (2000); S. Kajiwara, H. Nishino, and K. Kurosawa, Heterocycles, 54, 171 (2001); Y. R. Lee and B. S. Kim, Synth. Commun., 31, 381 (2001); G. Bar, A. F. Parsons, and C. B. Thomas, Chem. Commun., 2001, 1350; M. Yilmaz and A. T. Pekel, Synth. Commun., 31, 2189 (2001); G. Bar, A. F. Parsons, and C. B. Thomas, Tetrahedron, 57, 4719 (2001); V. Nair, P. M. Treesa, D. Maliakal, and N. P. Rath, Tetrahedron, 57, 7705 (2001); S. Muthusamy, C. Gunanathan, and S. A. Babu, Synlett, 2002, 787; Y. R. Lee, B. S. Kim, Y. U. Yung, W. S. Koh, J. S. Cha, and N. W. Kim, Synth. Commun., 32, 3099 (2002); M. C. S. de-Mattos, S. P. L. de-Souza, and S. M. Elias, Heterocycl. Commun., 9, 247 (2003); Y. R. Lee, K. Y. Kang, G. J. Lee, and W. K. Lee, Synthesis, 2003, 1977; N. N. Karade, S. G. Shirodkar, M. N. Patil, R. A. Potrekar, and H. N. Karade, Tetrahedron Lett., 44, 6729 (2003); R. Kumabe and H. Nishino, Heterocycl. Commun., 10, 135 (2004); V. Jadhav, M. Y. Park, and Y. H. Kim, Synthesis, 2004, 329 and references cited therein.
    • (2000) Tetrahedron , vol.56 , pp. 3867
    • Lee, Y.R.1    Kim, B.S.2    Kweon, H.I.3
  • 11
    • 0034734699 scopus 로고    scopus 로고
    • 3, have been used as a mediator for the cycloaddition reaction of 1,3-dicarbonyl and related compounds with alkenes forming 1,2-dihydrofuran derivatives. For earlier works: W. J. De Klein, "Organic Syntheses by Oxidation with Metal Compounds," ed. by W. J. Mijs and C. R. H. I. de Jonge, Plenum Press, New York (1986), Chapter 4; For recent reviews: V. Nair, J. Matthew, and J. Prabhakaran, Chem. Soc. Rev., 26, 127 (1997); J. Iqval and M. Mukhopadhyay, Synlett, 1997, 876; For more recent reports: Y. R. Lee, J. Y. Suk, and B. S. Kim, Org. Lett., 2, 1387 (2000); Y. R. Lee, B. S. Kim, and H. I. Kweon, Tetrahedron, 56, 3867 (2000); G. Bar, A. F. Parsons, and C. B. Thomas, Tetrahedron Lett., 41, 7751 (2000); Y. R. Lee, B. S. Kim, and D. H. Kim, Tetrahedron, 56, 8845 (2000); S. Kajiwara, H. Nishino, and K. Kurosawa, Heterocycles, 54, 171 (2001); Y. R. Lee and B. S. Kim, Synth. Commun., 31, 381 (2001); G. Bar, A. F. Parsons, and C. B. Thomas, Chem. Commun., 2001, 1350; M. Yilmaz and A. T. Pekel, Synth. Commun., 31, 2189 (2001); G. Bar, A. F. Parsons, and C. B. Thomas, Tetrahedron, 57, 4719 (2001); V. Nair, P. M. Treesa, D. Maliakal, and N. P. Rath, Tetrahedron, 57, 7705 (2001); S. Muthusamy, C. Gunanathan, and S. A. Babu, Synlett, 2002, 787; Y. R. Lee, B. S. Kim, Y. U. Yung, W. S. Koh, J. S. Cha, and N. W. Kim, Synth. Commun., 32, 3099 (2002); M. C. S. de-Mattos, S. P. L. de-Souza, and S. M. Elias, Heterocycl. Commun., 9, 247 (2003); Y. R. Lee, K. Y. Kang, G. J. Lee, and W. K. Lee, Synthesis, 2003, 1977; N. N. Karade, S. G. Shirodkar, M. N. Patil, R. A. Potrekar, and H. N. Karade, Tetrahedron Lett., 44, 6729 (2003); R. Kumabe and H. Nishino, Heterocycl. Commun., 10, 135 (2004); V. Jadhav, M. Y. Park, and Y. H. Kim, Synthesis, 2004, 329 and references cited therein.
    • (2000) Tetrahedron Lett. , vol.41 , pp. 7751
    • Bar, G.1    Parsons, A.F.2    Thomas, C.B.3
  • 12
    • 0034602142 scopus 로고    scopus 로고
    • 3, have been used as a mediator for the cycloaddition reaction of 1,3-dicarbonyl and related compounds with alkenes forming 1,2-dihydrofuran derivatives. For earlier works: W. J. De Klein, "Organic Syntheses by Oxidation with Metal Compounds," ed. by W. J. Mijs and C. R. H. I. de Jonge, Plenum Press, New York (1986), Chapter 4; For recent reviews: V. Nair, J. Matthew, and J. Prabhakaran, Chem. Soc. Rev., 26, 127 (1997); J. Iqval and M. Mukhopadhyay, Synlett, 1997, 876; For more recent reports: Y. R. Lee, J. Y. Suk, and B. S. Kim, Org. Lett., 2, 1387 (2000); Y. R. Lee, B. S. Kim, and H. I. Kweon, Tetrahedron, 56, 3867 (2000); G. Bar, A. F. Parsons, and C. B. Thomas, Tetrahedron Lett., 41, 7751 (2000); Y. R. Lee, B. S. Kim, and D. H. Kim, Tetrahedron, 56, 8845 (2000); S. Kajiwara, H. Nishino, and K. Kurosawa, Heterocycles, 54, 171 (2001); Y. R. Lee and B. S. Kim, Synth. Commun., 31, 381 (2001); G. Bar, A. F. Parsons, and C. B. Thomas, Chem. Commun., 2001, 1350; M. Yilmaz and A. T. Pekel, Synth. Commun., 31, 2189 (2001); G. Bar, A. F. Parsons, and C. B. Thomas, Tetrahedron, 57, 4719 (2001); V. Nair, P. M. Treesa, D. Maliakal, and N. P. Rath, Tetrahedron, 57, 7705 (2001); S. Muthusamy, C. Gunanathan, and S. A. Babu, Synlett, 2002, 787; Y. R. Lee, B. S. Kim, Y. U. Yung, W. S. Koh, J. S. Cha, and N. W. Kim, Synth. Commun., 32, 3099 (2002); M. C. S. de-Mattos, S. P. L. de-Souza, and S. M. Elias, Heterocycl. Commun., 9, 247 (2003); Y. R. Lee, K. Y. Kang, G. J. Lee, and W. K. Lee, Synthesis, 2003, 1977; N. N. Karade, S. G. Shirodkar, M. N. Patil, R. A. Potrekar, and H. N. Karade, Tetrahedron Lett., 44, 6729 (2003); R. Kumabe and H. Nishino, Heterocycl. Commun., 10, 135 (2004); V. Jadhav, M. Y. Park, and Y. H. Kim, Synthesis, 2004, 329 and references cited therein.
    • (2000) Tetrahedron , vol.56 , pp. 8845
    • Lee, Y.R.1    Kim, B.S.2    Kim, D.H.3
  • 13
    • 0035105372 scopus 로고    scopus 로고
    • 3, have been used as a mediator for the cycloaddition reaction of 1,3-dicarbonyl and related compounds with alkenes forming 1,2-dihydrofuran derivatives. For earlier works: W. J. De Klein, "Organic Syntheses by Oxidation with Metal Compounds," ed. by W. J. Mijs and C. R. H. I. de Jonge, Plenum Press, New York (1986), Chapter 4; For recent reviews: V. Nair, J. Matthew, and J. Prabhakaran, Chem. Soc. Rev., 26, 127 (1997); J. Iqval and M. Mukhopadhyay, Synlett, 1997, 876; For more recent reports: Y. R. Lee, J. Y. Suk, and B. S. Kim, Org. Lett., 2, 1387 (2000); Y. R. Lee, B. S. Kim, and H. I. Kweon, Tetrahedron, 56, 3867 (2000); G. Bar, A. F. Parsons, and C. B. Thomas, Tetrahedron Lett., 41, 7751 (2000); Y. R. Lee, B. S. Kim, and D. H. Kim, Tetrahedron, 56, 8845 (2000); S. Kajiwara, H. Nishino, and K. Kurosawa, Heterocycles, 54, 171 (2001); Y. R. Lee and B. S. Kim, Synth. Commun., 31, 381 (2001); G. Bar, A. F. Parsons, and C. B. Thomas, Chem. Commun., 2001, 1350; M. Yilmaz and A. T. Pekel, Synth. Commun., 31, 2189 (2001); G. Bar, A. F. Parsons, and C. B. Thomas, Tetrahedron, 57, 4719 (2001); V. Nair, P. M. Treesa, D. Maliakal, and N. P. Rath, Tetrahedron, 57, 7705 (2001); S. Muthusamy, C. Gunanathan, and S. A. Babu, Synlett, 2002, 787; Y. R. Lee, B. S. Kim, Y. U. Yung, W. S. Koh, J. S. Cha, and N. W. Kim, Synth. Commun., 32, 3099 (2002); M. C. S. de-Mattos, S. P. L. de-Souza, and S. M. Elias, Heterocycl. Commun., 9, 247 (2003); Y. R. Lee, K. Y. Kang, G. J. Lee, and W. K. Lee, Synthesis, 2003, 1977; N. N. Karade, S. G. Shirodkar, M. N. Patil, R. A. Potrekar, and H. N. Karade, Tetrahedron Lett., 44, 6729 (2003); R. Kumabe and H. Nishino, Heterocycl. Commun., 10, 135 (2004); V. Jadhav, M. Y. Park, and Y. H. Kim, Synthesis, 2004, 329 and references cited therein.
    • (2001) Heterocycles , vol.54 , pp. 171
    • Kajiwara, S.1    Nishino, H.2    Kurosawa, K.3
  • 14
    • 0035085221 scopus 로고    scopus 로고
    • 3, have been used as a mediator for the cycloaddition reaction of 1,3-dicarbonyl and related compounds with alkenes forming 1,2-dihydrofuran derivatives. For earlier works: W. J. De Klein, "Organic Syntheses by Oxidation with Metal Compounds," ed. by W. J. Mijs and C. R. H. I. de Jonge, Plenum Press, New York (1986), Chapter 4; For recent reviews: V. Nair, J. Matthew, and J. Prabhakaran, Chem. Soc. Rev., 26, 127 (1997); J. Iqval and M. Mukhopadhyay, Synlett, 1997, 876; For more recent reports: Y. R. Lee, J. Y. Suk, and B. S. Kim, Org. Lett., 2, 1387 (2000); Y. R. Lee, B. S. Kim, and H. I. Kweon, Tetrahedron, 56, 3867 (2000); G. Bar, A. F. Parsons, and C. B. Thomas, Tetrahedron Lett., 41, 7751 (2000); Y. R. Lee, B. S. Kim, and D. H. Kim, Tetrahedron, 56, 8845 (2000); S. Kajiwara, H. Nishino, and K. Kurosawa, Heterocycles, 54, 171 (2001); Y. R. Lee and B. S. Kim, Synth. Commun., 31, 381 (2001); G. Bar, A. F. Parsons, and C. B. Thomas, Chem. Commun., 2001, 1350; M. Yilmaz and A. T. Pekel, Synth. Commun., 31, 2189 (2001); G. Bar, A. F. Parsons, and C. B. Thomas, Tetrahedron, 57, 4719 (2001); V. Nair, P. M. Treesa, D. Maliakal, and N. P. Rath, Tetrahedron, 57, 7705 (2001); S. Muthusamy, C. Gunanathan, and S. A. Babu, Synlett, 2002, 787; Y. R. Lee, B. S. Kim, Y. U. Yung, W. S. Koh, J. S. Cha, and N. W. Kim, Synth. Commun., 32, 3099 (2002); M. C. S. de-Mattos, S. P. L. de-Souza, and S. M. Elias, Heterocycl. Commun., 9, 247 (2003); Y. R. Lee, K. Y. Kang, G. J. Lee, and W. K. Lee, Synthesis, 2003, 1977; N. N. Karade, S. G. Shirodkar, M. N. Patil, R. A. Potrekar, and H. N. Karade, Tetrahedron Lett., 44, 6729 (2003); R. Kumabe and H. Nishino, Heterocycl. Commun., 10, 135 (2004); V. Jadhav, M. Y. Park, and Y. H. Kim, Synthesis, 2004, 329 and references cited therein.
    • (2001) Synth. Commun. , vol.31 , pp. 381
    • Lee, Y.R.1    Kim, B.S.2
  • 15
    • 0035822758 scopus 로고    scopus 로고
    • 3, have been used as a mediator for the cycloaddition reaction of 1,3-dicarbonyl and related compounds with alkenes forming 1,2-dihydrofuran derivatives. For earlier works: W. J. De Klein, "Organic Syntheses by Oxidation with Metal Compounds," ed. by W. J. Mijs and C. R. H. I. de Jonge, Plenum Press, New York (1986), Chapter 4; For recent reviews: V. Nair, J. Matthew, and J. Prabhakaran, Chem. Soc. Rev., 26, 127 (1997); J. Iqval and M. Mukhopadhyay, Synlett, 1997, 876; For more recent reports: Y. R. Lee, J. Y. Suk, and B. S. Kim, Org. Lett., 2, 1387 (2000); Y. R. Lee, B. S. Kim, and H. I. Kweon, Tetrahedron, 56, 3867 (2000); G. Bar, A. F. Parsons, and C. B. Thomas, Tetrahedron Lett., 41, 7751 (2000); Y. R. Lee, B. S. Kim, and D. H. Kim, Tetrahedron, 56, 8845 (2000); S. Kajiwara, H. Nishino, and K. Kurosawa, Heterocycles, 54, 171 (2001); Y. R. Lee and B. S. Kim, Synth. Commun., 31, 381 (2001); G. Bar, A. F. Parsons, and C. B. Thomas, Chem. Commun., 2001, 1350; M. Yilmaz and A. T. Pekel, Synth. Commun., 31, 2189 (2001); G. Bar, A. F. Parsons, and C. B. Thomas, Tetrahedron, 57, 4719 (2001); V. Nair, P. M. Treesa, D. Maliakal, and N. P. Rath, Tetrahedron, 57, 7705 (2001); S. Muthusamy, C. Gunanathan, and S. A. Babu, Synlett, 2002, 787; Y. R. Lee, B. S. Kim, Y. U. Yung, W. S. Koh, J. S. Cha, and N. W. Kim, Synth. Commun., 32, 3099 (2002); M. C. S. de-Mattos, S. P. L. de-Souza, and S. M. Elias, Heterocycl. Commun., 9, 247 (2003); Y. R. Lee, K. Y. Kang, G. J. Lee, and W. K. Lee, Synthesis, 2003, 1977; N. N. Karade, S. G. Shirodkar, M. N. Patil, R. A. Potrekar, and H. N. Karade, Tetrahedron Lett., 44, 6729 (2003); R. Kumabe and H. Nishino, Heterocycl. Commun., 10, 135 (2004); V. Jadhav, M. Y. Park, and Y. H. Kim, Synthesis, 2004, 329 and references cited therein.
    • (2001) Chem. Commun. , pp. 1350
    • Bar, G.1    Parsons, A.F.2    Thomas, C.B.3
  • 16
    • 0034895562 scopus 로고    scopus 로고
    • 3, have been used as a mediator for the cycloaddition reaction of 1,3-dicarbonyl and related compounds with alkenes forming 1,2-dihydrofuran derivatives. For earlier works: W. J. De Klein, "Organic Syntheses by Oxidation with Metal Compounds," ed. by W. J. Mijs and C. R. H. I. de Jonge, Plenum Press, New York (1986), Chapter 4; For recent reviews: V. Nair, J. Matthew, and J. Prabhakaran, Chem. Soc. Rev., 26, 127 (1997); J. Iqval and M. Mukhopadhyay, Synlett, 1997, 876; For more recent reports: Y. R. Lee, J. Y. Suk, and B. S. Kim, Org. Lett., 2, 1387 (2000); Y. R. Lee, B. S. Kim, and H. I. Kweon, Tetrahedron, 56, 3867 (2000); G. Bar, A. F. Parsons, and C. B. Thomas, Tetrahedron Lett., 41, 7751 (2000); Y. R. Lee, B. S. Kim, and D. H. Kim, Tetrahedron, 56, 8845 (2000); S. Kajiwara, H. Nishino, and K. Kurosawa, Heterocycles, 54, 171 (2001); Y. R. Lee and B. S. Kim, Synth. Commun., 31, 381 (2001); G. Bar, A. F. Parsons, and C. B. Thomas, Chem. Commun., 2001, 1350; M. Yilmaz and A. T. Pekel, Synth. Commun., 31, 2189 (2001); G. Bar, A. F. Parsons, and C. B. Thomas, Tetrahedron, 57, 4719 (2001); V. Nair, P. M. Treesa, D. Maliakal, and N. P. Rath, Tetrahedron, 57, 7705 (2001); S. Muthusamy, C. Gunanathan, and S. A. Babu, Synlett, 2002, 787; Y. R. Lee, B. S. Kim, Y. U. Yung, W. S. Koh, J. S. Cha, and N. W. Kim, Synth. Commun., 32, 3099 (2002); M. C. S. de-Mattos, S. P. L. de-Souza, and S. M. Elias, Heterocycl. Commun., 9, 247 (2003); Y. R. Lee, K. Y. Kang, G. J. Lee, and W. K. Lee, Synthesis, 2003, 1977; N. N. Karade, S. G. Shirodkar, M. N. Patil, R. A. Potrekar, and H. N. Karade, Tetrahedron Lett., 44, 6729 (2003); R. Kumabe and H. Nishino, Heterocycl. Commun., 10, 135 (2004); V. Jadhav, M. Y. Park, and Y. H. Kim, Synthesis, 2004, 329 and references cited therein.
    • (2001) Synth. Commun. , vol.31 , pp. 2189
    • Yilmaz, M.1    Pekel, A.T.2
  • 17
    • 0035962679 scopus 로고    scopus 로고
    • 3, have been used as a mediator for the cycloaddition reaction of 1,3-dicarbonyl and related compounds with alkenes forming 1,2-dihydrofuran derivatives. For earlier works: W. J. De Klein, "Organic Syntheses by Oxidation with Metal Compounds," ed. by W. J. Mijs and C. R. H. I. de Jonge, Plenum Press, New York (1986), Chapter 4; For recent reviews: V. Nair, J. Matthew, and J. Prabhakaran, Chem. Soc. Rev., 26, 127 (1997); J. Iqval and M. Mukhopadhyay, Synlett, 1997, 876; For more recent reports: Y. R. Lee, J. Y. Suk, and B. S. Kim, Org. Lett., 2, 1387 (2000); Y. R. Lee, B. S. Kim, and H. I. Kweon, Tetrahedron, 56, 3867 (2000); G. Bar, A. F. Parsons, and C. B. Thomas, Tetrahedron Lett., 41, 7751 (2000); Y. R. Lee, B. S. Kim, and D. H. Kim, Tetrahedron, 56, 8845 (2000); S. Kajiwara, H. Nishino, and K. Kurosawa, Heterocycles, 54, 171 (2001); Y. R. Lee and B. S. Kim, Synth. Commun., 31, 381 (2001); G. Bar, A. F. Parsons, and C. B. Thomas, Chem. Commun., 2001, 1350; M. Yilmaz and A. T. Pekel, Synth. Commun., 31, 2189 (2001); G. Bar, A. F. Parsons, and C. B. Thomas, Tetrahedron, 57, 4719 (2001); V. Nair, P. M. Treesa, D. Maliakal, and N. P. Rath, Tetrahedron, 57, 7705 (2001); S. Muthusamy, C. Gunanathan, and S. A. Babu, Synlett, 2002, 787; Y. R. Lee, B. S. Kim, Y. U. Yung, W. S. Koh, J. S. Cha, and N. W. Kim, Synth. Commun., 32, 3099 (2002); M. C. S. de-Mattos, S. P. L. de-Souza, and S. M. Elias, Heterocycl. Commun., 9, 247 (2003); Y. R. Lee, K. Y. Kang, G. J. Lee, and W. K. Lee, Synthesis, 2003, 1977; N. N. Karade, S. G. Shirodkar, M. N. Patil, R. A. Potrekar, and H. N. Karade, Tetrahedron Lett., 44, 6729 (2003); R. Kumabe and H. Nishino, Heterocycl. Commun., 10, 135 (2004); V. Jadhav, M. Y. Park, and Y. H. Kim, Synthesis, 2004, 329 and references cited therein.
    • (2001) Tetrahedron , vol.57 , pp. 4719
    • Bar, G.1    Parsons, A.F.2    Thomas, C.B.3
  • 18
    • 0035801896 scopus 로고    scopus 로고
    • 3, have been used as a mediator for the cycloaddition reaction of 1,3-dicarbonyl and related compounds with alkenes forming 1,2-dihydrofuran derivatives. For earlier works: W. J. De Klein, "Organic Syntheses by Oxidation with Metal Compounds," ed. by W. J. Mijs and C. R. H. I. de Jonge, Plenum Press, New York (1986), Chapter 4; For recent reviews: V. Nair, J. Matthew, and J. Prabhakaran, Chem. Soc. Rev., 26, 127 (1997); J. Iqval and M. Mukhopadhyay, Synlett, 1997, 876; For more recent reports: Y. R. Lee, J. Y. Suk, and B. S. Kim, Org. Lett., 2, 1387 (2000); Y. R. Lee, B. S. Kim, and H. I. Kweon, Tetrahedron, 56, 3867 (2000); G. Bar, A. F. Parsons, and C. B. Thomas, Tetrahedron Lett., 41, 7751 (2000); Y. R. Lee, B. S. Kim, and D. H. Kim, Tetrahedron, 56, 8845 (2000); S. Kajiwara, H. Nishino, and K. Kurosawa, Heterocycles, 54, 171 (2001); Y. R. Lee and B. S. Kim, Synth. Commun., 31, 381 (2001); G. Bar, A. F. Parsons, and C. B. Thomas, Chem. Commun., 2001, 1350; M. Yilmaz and A. T. Pekel, Synth. Commun., 31, 2189 (2001); G. Bar, A. F. Parsons, and C. B. Thomas, Tetrahedron, 57, 4719 (2001); V. Nair, P. M. Treesa, D. Maliakal, and N. P. Rath, Tetrahedron, 57, 7705 (2001); S. Muthusamy, C. Gunanathan, and S. A. Babu, Synlett, 2002, 787; Y. R. Lee, B. S. Kim, Y. U. Yung, W. S. Koh, J. S. Cha, and N. W. Kim, Synth. Commun., 32, 3099 (2002); M. C. S. de-Mattos, S. P. L. de-Souza, and S. M. Elias, Heterocycl. Commun., 9, 247 (2003); Y. R. Lee, K. Y. Kang, G. J. Lee, and W. K. Lee, Synthesis, 2003, 1977; N. N. Karade, S. G. Shirodkar, M. N. Patil, R. A. Potrekar, and H. N. Karade, Tetrahedron Lett., 44, 6729 (2003); R. Kumabe and H. Nishino, Heterocycl. Commun., 10, 135 (2004); V. Jadhav, M. Y. Park, and Y. H. Kim, Synthesis, 2004, 329 and references cited therein.
    • (2001) Tetrahedron , vol.57 , pp. 7705
    • Nair, V.1    Treesa, P.M.2    Maliakal, D.3    Rath, N.P.4
  • 19
    • 0036250593 scopus 로고    scopus 로고
    • 3, have been used as a mediator for the cycloaddition reaction of 1,3-dicarbonyl and related compounds with alkenes forming 1,2-dihydrofuran derivatives. For earlier works: W. J. De Klein, "Organic Syntheses by Oxidation with Metal Compounds," ed. by W. J. Mijs and C. R. H. I. de Jonge, Plenum Press, New York (1986), Chapter 4; For recent reviews: V. Nair, J. Matthew, and J. Prabhakaran, Chem. Soc. Rev., 26, 127 (1997); J. Iqval and M. Mukhopadhyay, Synlett, 1997, 876; For more recent reports: Y. R. Lee, J. Y. Suk, and B. S. Kim, Org. Lett., 2, 1387 (2000); Y. R. Lee, B. S. Kim, and H. I. Kweon, Tetrahedron, 56, 3867 (2000); G. Bar, A. F. Parsons, and C. B. Thomas, Tetrahedron Lett., 41, 7751 (2000); Y. R. Lee, B. S. Kim, and D. H. Kim, Tetrahedron, 56, 8845 (2000); S. Kajiwara, H. Nishino, and K. Kurosawa, Heterocycles, 54, 171 (2001); Y. R. Lee and B. S. Kim, Synth. Commun., 31, 381 (2001); G. Bar, A. F. Parsons, and C. B. Thomas, Chem. Commun., 2001, 1350; M. Yilmaz and A. T. Pekel, Synth. Commun., 31, 2189 (2001); G. Bar, A. F. Parsons, and C. B. Thomas, Tetrahedron, 57, 4719 (2001); V. Nair, P. M. Treesa, D. Maliakal, and N. P. Rath, Tetrahedron, 57, 7705 (2001); S. Muthusamy, C. Gunanathan, and S. A. Babu, Synlett, 2002, 787; Y. R. Lee, B. S. Kim, Y. U. Yung, W. S. Koh, J. S. Cha, and N. W. Kim, Synth. Commun., 32, 3099 (2002); M. C. S. de-Mattos, S. P. L. de-Souza, and S. M. Elias, Heterocycl. Commun., 9, 247 (2003); Y. R. Lee, K. Y. Kang, G. J. Lee, and W. K. Lee, Synthesis, 2003, 1977; N. N. Karade, S. G. Shirodkar, M. N. Patil, R. A. Potrekar, and H. N. Karade, Tetrahedron Lett., 44, 6729 (2003); R. Kumabe and H. Nishino, Heterocycl. Commun., 10, 135 (2004); V. Jadhav, M. Y. Park, and Y. H. Kim, Synthesis, 2004, 329 and references cited therein.
    • (2002) Synlett , pp. 787
    • Muthusamy, S.1    Gunanathan, C.2    Babu, S.A.3
  • 20
    • 0036380512 scopus 로고    scopus 로고
    • 3, have been used as a mediator for the cycloaddition reaction of 1,3-dicarbonyl and related compounds with alkenes forming 1,2-dihydrofuran derivatives. For earlier works: W. J. De Klein, "Organic Syntheses by Oxidation with Metal Compounds," ed. by W. J. Mijs and C. R. H. I. de Jonge, Plenum Press, New York (1986), Chapter 4; For recent reviews: V. Nair, J. Matthew, and J. Prabhakaran, Chem. Soc. Rev., 26, 127 (1997); J. Iqval and M. Mukhopadhyay, Synlett, 1997, 876; For more recent reports: Y. R. Lee, J. Y. Suk, and B. S. Kim, Org. Lett., 2, 1387 (2000); Y. R. Lee, B. S. Kim, and H. I. Kweon, Tetrahedron, 56, 3867 (2000); G. Bar, A. F. Parsons, and C. B. Thomas, Tetrahedron Lett., 41, 7751 (2000); Y. R. Lee, B. S. Kim, and D. H. Kim, Tetrahedron, 56, 8845 (2000); S. Kajiwara, H. Nishino, and K. Kurosawa, Heterocycles, 54, 171 (2001); Y. R. Lee and B. S. Kim, Synth. Commun., 31, 381 (2001); G. Bar, A. F. Parsons, and C. B. Thomas, Chem. Commun., 2001, 1350; M. Yilmaz and A. T. Pekel, Synth. Commun., 31, 2189 (2001); G. Bar, A. F. Parsons, and C. B. Thomas, Tetrahedron, 57, 4719 (2001); V. Nair, P. M. Treesa, D. Maliakal, and N. P. Rath, Tetrahedron, 57, 7705 (2001); S. Muthusamy, C. Gunanathan, and S. A. Babu, Synlett, 2002, 787; Y. R. Lee, B. S. Kim, Y. U. Yung, W. S. Koh, J. S. Cha, and N. W. Kim, Synth. Commun., 32, 3099 (2002); M. C. S. de-Mattos, S. P. L. de-Souza, and S. M. Elias, Heterocycl. Commun., 9, 247 (2003); Y. R. Lee, K. Y. Kang, G. J. Lee, and W. K. Lee, Synthesis, 2003, 1977; N. N. Karade, S. G. Shirodkar, M. N. Patil, R. A. Potrekar, and H. N. Karade, Tetrahedron Lett., 44, 6729 (2003); R. Kumabe and H. Nishino, Heterocycl. Commun., 10, 135 (2004); V. Jadhav, M. Y. Park, and Y. H. Kim, Synthesis, 2004, 329 and references cited therein.
    • (2002) Synth. Commun. , vol.32 , pp. 3099
    • Lee, Y.R.1    Kim, B.S.2    Yung, Y.U.3    Koh, W.S.4    Cha, J.S.5    Kim, N.W.6
  • 21
    • 0141992057 scopus 로고    scopus 로고
    • 3, have been used as a mediator for the cycloaddition reaction of 1,3-dicarbonyl and related compounds with alkenes forming 1,2-dihydrofuran derivatives. For earlier works: W. J. De Klein, "Organic Syntheses by Oxidation with Metal Compounds," ed. by W. J. Mijs and C. R. H. I. de Jonge, Plenum Press, New York (1986), Chapter 4; For recent reviews: V. Nair, J. Matthew, and J. Prabhakaran, Chem. Soc. Rev., 26, 127 (1997); J. Iqval and M. Mukhopadhyay, Synlett, 1997, 876; For more recent reports: Y. R. Lee, J. Y. Suk, and B. S. Kim, Org. Lett., 2, 1387 (2000); Y. R. Lee, B. S. Kim, and H. I. Kweon, Tetrahedron, 56, 3867 (2000); G. Bar, A. F. Parsons, and C. B. Thomas, Tetrahedron Lett., 41, 7751 (2000); Y. R. Lee, B. S. Kim, and D. H. Kim, Tetrahedron, 56, 8845 (2000); S. Kajiwara, H. Nishino, and K. Kurosawa, Heterocycles, 54, 171 (2001); Y. R. Lee and B. S. Kim, Synth. Commun., 31, 381 (2001); G. Bar, A. F. Parsons, and C. B. Thomas, Chem. Commun., 2001, 1350; M. Yilmaz and A. T. Pekel, Synth. Commun., 31, 2189 (2001); G. Bar, A. F. Parsons, and C. B. Thomas, Tetrahedron, 57, 4719 (2001); V. Nair, P. M. Treesa, D. Maliakal, and N. P. Rath, Tetrahedron, 57, 7705 (2001); S. Muthusamy, C. Gunanathan, and S. A. Babu, Synlett, 2002, 787; Y. R. Lee, B. S. Kim, Y. U. Yung, W. S. Koh, J. S. Cha, and N. W. Kim, Synth. Commun., 32, 3099 (2002); M. C. S. de-Mattos, S. P. L. de-Souza, and S. M. Elias, Heterocycl. Commun., 9, 247 (2003); Y. R. Lee, K. Y. Kang, G. J. Lee, and W. K. Lee, Synthesis, 2003, 1977; N. N. Karade, S. G. Shirodkar, M. N. Patil, R. A. Potrekar, and H. N. Karade, Tetrahedron Lett., 44, 6729 (2003); R. Kumabe and H. Nishino, Heterocycl. Commun., 10, 135 (2004); V. Jadhav, M. Y. Park, and Y. H. Kim, Synthesis, 2004, 329 and references cited therein.
    • (2003) Heterocycl. Commun. , vol.9 , pp. 247
    • De-Mattos, M.C.S.1    De-Souza, S.P.L.2    Elias, S.M.3
  • 22
    • 0141618326 scopus 로고    scopus 로고
    • 3, have been used as a mediator for the cycloaddition reaction of 1,3-dicarbonyl and related compounds with alkenes forming 1,2-dihydrofuran derivatives. For earlier works: W. J. De Klein, "Organic Syntheses by Oxidation with Metal Compounds," ed. by W. J. Mijs and C. R. H. I. de Jonge, Plenum Press, New York (1986), Chapter 4; For recent reviews: V. Nair, J. Matthew, and J. Prabhakaran, Chem. Soc. Rev., 26, 127 (1997); J. Iqval and M. Mukhopadhyay, Synlett, 1997, 876; For more recent reports: Y. R. Lee, J. Y. Suk, and B. S. Kim, Org. Lett., 2, 1387 (2000); Y. R. Lee, B. S. Kim, and H. I. Kweon, Tetrahedron, 56, 3867 (2000); G. Bar, A. F. Parsons, and C. B. Thomas, Tetrahedron Lett., 41, 7751 (2000); Y. R. Lee, B. S. Kim, and D. H. Kim, Tetrahedron, 56, 8845 (2000); S. Kajiwara, H. Nishino, and K. Kurosawa, Heterocycles, 54, 171 (2001); Y. R. Lee and B. S. Kim, Synth. Commun., 31, 381 (2001); G. Bar, A. F. Parsons, and C. B. Thomas, Chem. Commun., 2001, 1350; M. Yilmaz and A. T. Pekel, Synth. Commun., 31, 2189 (2001); G. Bar, A. F. Parsons, and C. B. Thomas, Tetrahedron, 57, 4719 (2001); V. Nair, P. M. Treesa, D. Maliakal, and N. P. Rath, Tetrahedron, 57, 7705 (2001); S. Muthusamy, C. Gunanathan, and S. A. Babu, Synlett, 2002, 787; Y. R. Lee, B. S. Kim, Y. U. Yung, W. S. Koh, J. S. Cha, and N. W. Kim, Synth. Commun., 32, 3099 (2002); M. C. S. de-Mattos, S. P. L. de-Souza, and S. M. Elias, Heterocycl. Commun., 9, 247 (2003); Y. R. Lee, K. Y. Kang, G. J. Lee, and W. K. Lee, Synthesis, 2003, 1977; N. N. Karade, S. G. Shirodkar, M. N. Patil, R. A. Potrekar, and H. N. Karade, Tetrahedron Lett., 44, 6729 (2003); R. Kumabe and H. Nishino, Heterocycl. Commun., 10, 135 (2004); V. Jadhav, M. Y. Park, and Y. H. Kim, Synthesis, 2004, 329 and references cited therein.
    • (2003) Synthesis , pp. 1977
    • Lee, Y.R.1    Kang, K.Y.2    Lee, G.J.3    Lee, W.K.4
  • 23
    • 0041669220 scopus 로고    scopus 로고
    • 3, have been used as a mediator for the cycloaddition reaction of 1,3-dicarbonyl and related compounds with alkenes forming 1,2-dihydrofuran derivatives. For earlier works: W. J. De Klein, "Organic Syntheses by Oxidation with Metal Compounds," ed. by W. J. Mijs and C. R. H. I. de Jonge, Plenum Press, New York (1986), Chapter 4; For recent reviews: V. Nair, J. Matthew, and J. Prabhakaran, Chem. Soc. Rev., 26, 127 (1997); J. Iqval and M. Mukhopadhyay, Synlett, 1997, 876; For more recent reports: Y. R. Lee, J. Y. Suk, and B. S. Kim, Org. Lett., 2, 1387 (2000); Y. R. Lee, B. S. Kim, and H. I. Kweon, Tetrahedron, 56, 3867 (2000); G. Bar, A. F. Parsons, and C. B. Thomas, Tetrahedron Lett., 41, 7751 (2000); Y. R. Lee, B. S. Kim, and D. H. Kim, Tetrahedron, 56, 8845 (2000); S. Kajiwara, H. Nishino, and K. Kurosawa, Heterocycles, 54, 171 (2001); Y. R. Lee and B. S. Kim, Synth. Commun., 31, 381 (2001); G. Bar, A. F. Parsons, and C. B. Thomas, Chem. Commun., 2001, 1350; M. Yilmaz and A. T. Pekel, Synth. Commun., 31, 2189 (2001); G. Bar, A. F. Parsons, and C. B. Thomas, Tetrahedron, 57, 4719 (2001); V. Nair, P. M. Treesa, D. Maliakal, and N. P. Rath, Tetrahedron, 57, 7705 (2001); S. Muthusamy, C. Gunanathan, and S. A. Babu, Synlett, 2002, 787; Y. R. Lee, B. S. Kim, Y. U. Yung, W. S. Koh, J. S. Cha, and N. W. Kim, Synth. Commun., 32, 3099 (2002); M. C. S. de-Mattos, S. P. L. de-Souza, and S. M. Elias, Heterocycl. Commun., 9, 247 (2003); Y. R. Lee, K. Y. Kang, G. J. Lee, and W. K. Lee, Synthesis, 2003, 1977; N. N. Karade, S. G. Shirodkar, M. N. Patil, R. A. Potrekar, and H. N. Karade, Tetrahedron Lett., 44, 6729 (2003); R. Kumabe and H. Nishino, Heterocycl. Commun., 10, 135 (2004); V. Jadhav, M. Y. Park, and Y. H. Kim, Synthesis, 2004, 329 and references cited therein.
    • (2003) Tetrahedron Lett. , vol.44 , pp. 6729
    • Karade, N.N.1    Shirodkar, S.G.2    Patil, M.N.3    Potrekar, R.A.4    Karade, H.N.5
  • 24
    • 3042752060 scopus 로고    scopus 로고
    • 3, have been used as a mediator for the cycloaddition reaction of 1,3-dicarbonyl and related compounds with alkenes forming 1,2-dihydrofuran derivatives. For earlier works: W. J. De Klein, "Organic Syntheses by Oxidation with Metal Compounds," ed. by W. J. Mijs and C. R. H. I. de Jonge, Plenum Press, New York (1986), Chapter 4; For recent reviews: V. Nair, J. Matthew, and J. Prabhakaran, Chem. Soc. Rev., 26, 127 (1997); J. Iqval and M. Mukhopadhyay, Synlett, 1997, 876; For more recent reports: Y. R. Lee, J. Y. Suk, and B. S. Kim, Org. Lett., 2, 1387 (2000); Y. R. Lee, B. S. Kim, and H. I. Kweon, Tetrahedron, 56, 3867 (2000); G. Bar, A. F. Parsons, and C. B. Thomas, Tetrahedron Lett., 41, 7751 (2000); Y. R. Lee, B. S. Kim, and D. H. Kim, Tetrahedron, 56, 8845 (2000); S. Kajiwara, H. Nishino, and K. Kurosawa, Heterocycles, 54, 171 (2001); Y. R. Lee and B. S. Kim, Synth. Commun., 31, 381 (2001); G. Bar, A. F. Parsons, and C. B. Thomas, Chem. Commun., 2001, 1350; M. Yilmaz and A. T. Pekel, Synth. Commun., 31, 2189 (2001); G. Bar, A. F. Parsons, and C. B. Thomas, Tetrahedron, 57, 4719 (2001); V. Nair, P. M. Treesa, D. Maliakal, and N. P. Rath, Tetrahedron, 57, 7705 (2001); S. Muthusamy, C. Gunanathan, and S. A. Babu, Synlett, 2002, 787; Y. R. Lee, B. S. Kim, Y. U. Yung, W. S. Koh, J. S. Cha, and N. W. Kim, Synth. Commun., 32, 3099 (2002); M. C. S. de-Mattos, S. P. L. de-Souza, and S. M. Elias, Heterocycl. Commun., 9, 247 (2003); Y. R. Lee, K. Y. Kang, G. J. Lee, and W. K. Lee, Synthesis, 2003, 1977; N. N. Karade, S. G. Shirodkar, M. N. Patil, R. A. Potrekar, and H. N. Karade, Tetrahedron Lett., 44, 6729 (2003); R. Kumabe and H. Nishino, Heterocycl. Commun., 10, 135 (2004); V. Jadhav, M. Y. Park, and Y. H. Kim, Synthesis, 2004, 329 and references cited therein.
    • (2004) Heterocycl. Commun. , vol.10 , pp. 135
    • Kumabe, R.1    Nishino, H.2
  • 25
    • 1442359963 scopus 로고    scopus 로고
    • and references cited therein
    • 3, have been used as a mediator for the cycloaddition reaction of 1,3-dicarbonyl and related compounds with alkenes forming 1,2-dihydrofuran derivatives. For earlier works: W. J. De Klein, "Organic Syntheses by Oxidation with Metal Compounds," ed. by W. J. Mijs and C. R. H. I. de Jonge, Plenum Press, New York (1986), Chapter 4; For recent reviews: V. Nair, J. Matthew, and J. Prabhakaran, Chem. Soc. Rev., 26, 127 (1997); J. Iqval and M. Mukhopadhyay, Synlett, 1997, 876; For more recent reports: Y. R. Lee, J. Y. Suk, and B. S. Kim, Org. Lett., 2, 1387 (2000); Y. R. Lee, B. S. Kim, and H. I. Kweon, Tetrahedron, 56, 3867 (2000); G. Bar, A. F. Parsons, and C. B. Thomas, Tetrahedron Lett., 41, 7751 (2000); Y. R. Lee, B. S. Kim, and D. H. Kim, Tetrahedron, 56, 8845 (2000); S. Kajiwara, H. Nishino, and K. Kurosawa, Heterocycles, 54, 171 (2001); Y. R. Lee and B. S. Kim, Synth. Commun., 31, 381 (2001); G. Bar, A. F. Parsons, and C. B. Thomas, Chem. Commun., 2001, 1350; M. Yilmaz and A. T. Pekel, Synth. Commun., 31, 2189 (2001); G. Bar, A. F. Parsons, and C. B. Thomas, Tetrahedron, 57, 4719 (2001); V. Nair, P. M. Treesa, D. Maliakal, and N. P. Rath, Tetrahedron, 57, 7705 (2001); S. Muthusamy, C. Gunanathan, and S. A. Babu, Synlett, 2002, 787; Y. R. Lee, B. S. Kim, Y. U. Yung, W. S. Koh, J. S. Cha, and N. W. Kim, Synth. Commun., 32, 3099 (2002); M. C. S. de-Mattos, S. P. L. de-Souza, and S. M. Elias, Heterocycl. Commun., 9, 247 (2003); Y. R. Lee, K. Y. Kang, G. J. Lee, and W. K. Lee, Synthesis, 2003, 1977; N. N. Karade, S. G. Shirodkar, M. N. Patil, R. A. Potrekar, and H. N. Karade, Tetrahedron Lett., 44, 6729 (2003); R. Kumabe and H. Nishino, Heterocycl. Commun., 10, 135 (2004); V. Jadhav, M. Y. Park, and Y. H. Kim, Synthesis, 2004, 329 and references cited therein.
    • (2004) Synthesis , pp. 329
    • Jadhav, V.1    Park, M.Y.2    Kim, Y.H.3
  • 27
    • 0001556501 scopus 로고
    • Previous syntheses of furo[3,2-c]oxepin-4-one derivatives: D. P. Curran, T. M. Morgan, C. E. Schwartz, B. B. Snider, and M. A. Dombroski, J. Am. Chem. Soc., 113, 6607 (1991); H. A. Stefani, N. Petragnani, C. J. Valduga, and S. A. Brandt, Teterahedron Lett., 38, 4977 (1997); A. Lattanzi, P. Iannece, and A. Scettri, Teterahedron Lett., 40, 3899 (1999).
    • (1991) J. Am. Chem. Soc. , vol.113 , pp. 6607
    • Curran, D.P.1    Morgan, T.M.2    Schwartz, C.E.3    Snider, B.B.4    Dombroski, M.A.5
  • 28
    • 0030861432 scopus 로고    scopus 로고
    • Previous syntheses of furo[3,2-c]oxepin-4-one derivatives: D. P. Curran, T. M. Morgan, C. E. Schwartz, B. B. Snider, and M. A. Dombroski, J. Am. Chem. Soc., 113, 6607 (1991); H. A. Stefani, N. Petragnani, C. J. Valduga, and S. A. Brandt, Teterahedron Lett., 38, 4977 (1997); A. Lattanzi, P. Iannece, and A. Scettri, Teterahedron Lett., 40, 3899 (1999).
    • (1997) Teterahedron Lett. , vol.38 , pp. 4977
    • Stefani, H.A.1    Petragnani, N.2    Valduga, C.J.3    Brandt, S.A.4
  • 29
    • 0033553488 scopus 로고    scopus 로고
    • Previous syntheses of furo[3,2-c]oxepin-4-one derivatives: D. P. Curran, T. M. Morgan, C. E. Schwartz, B. B. Snider, and M. A. Dombroski, J. Am. Chem. Soc., 113, 6607 (1991); H. A. Stefani, N. Petragnani, C. J. Valduga, and S. A. Brandt, Teterahedron Lett., 38, 4977 (1997); A. Lattanzi, P. Iannece, and A. Scettri, Teterahedron Lett., 40, 3899 (1999).
    • (1999) Teterahedron Lett. , vol.40 , pp. 3899
    • Lattanzi, A.1    Iannece, P.2    Scettri, A.3
  • 30
    • 14844284103 scopus 로고    scopus 로고
    • note
    • +, 6.7), 191 (6.9), 152 (99), 124 (100).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.