메뉴 건너뛰기




Volumn 68, Issue 4, 2003, Pages 1633-1635

A novel titanium-catalyzed cyclization of olefinic iodoethers to tetrahydrofurans

Author keywords

[No Author keywords available]

Indexed keywords

CATALYST ACTIVITY; ETHERS; TITANIUM;

EID: 0242600606     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo026290e     Document Type: Article
Times cited : (18)

References (38)
  • 1
    • 0003587524 scopus 로고
    • Pergmon Press: Oxford, UK
    • For a general review and book, see: (a) Giese, B. Radical in Organic Synthesis: Formation of C- C Bonds; Pergmon Press: Oxford, UK, 1986. (b) Curran, D. P. Synthesis 1988, 417 and 489. (c) Curran, D. P. In Comprehensive Organic Synthesis; Trost, B. M., Flamin, I., Semmelhack, M. F., Eds.; Pergmon Press: Oxford, UK, 1991; Vol. 4, pp 715 and 779. (d) Motherwell, W. B.; Crich, D. Free Radical Chain Reactions in Organic Synthesis; Academic Press: London, UK, 1992. (e) Fossey, J.; Lefort, D.; Sorba, J. Free Radical in Organic Chemistry; Wiley: New York, 1995.
    • (1986) Radical in Organic Synthesis: Formation of C-C Bonds
    • Giese, B.1
  • 2
    • 85082777144 scopus 로고
    • For a general review and book, see: (a) Giese, B. Radical in Organic Synthesis: Formation of C- C Bonds; Pergmon Press: Oxford, UK, 1986. (b) Curran, D. P. Synthesis 1988, 417 and 489. (c) Curran, D. P. In Comprehensive Organic Synthesis; Trost, B. M., Flamin, I., Semmelhack, M. F., Eds.; Pergmon Press: Oxford, UK, 1991; Vol. 4, pp 715 and 779. (d) Motherwell, W. B.; Crich, D. Free Radical Chain Reactions in Organic Synthesis; Academic Press: London, UK, 1992. (e) Fossey, J.; Lefort, D.; Sorba, J. Free Radical in Organic Chemistry; Wiley: New York, 1995.
    • (1988) Synthesis , pp. 417
    • Curran, D.P.1
  • 3
    • 0001216647 scopus 로고
    • Trost, B. M., Flamin, I., Semmelhack, M. F., Eds.; Pergmon Press: Oxford, UK
    • For a general review and book, see: (a) Giese, B. Radical in Organic Synthesis: Formation of C- C Bonds; Pergmon Press: Oxford, UK, 1986. (b) Curran, D. P. Synthesis 1988, 417 and 489. (c) Curran, D. P. In Comprehensive Organic Synthesis; Trost, B. M., Flamin, I., Semmelhack, M. F., Eds.; Pergmon Press: Oxford, UK, 1991; Vol. 4, pp 715 and 779. (d) Motherwell, W. B.; Crich, D. Free Radical Chain Reactions in Organic Synthesis; Academic Press: London, UK, 1992. (e) Fossey, J.; Lefort, D.; Sorba, J. Free Radical in Organic Chemistry; Wiley: New York, 1995.
    • (1991) Comprehensive Organic Synthesis , vol.4 , pp. 715
    • Curran, D.P.1
  • 4
    • 0003573892 scopus 로고
    • Academic Press: London, UK
    • For a general review and book, see: (a) Giese, B. Radical in Organic Synthesis: Formation of C- C Bonds; Pergmon Press: Oxford, UK, 1986. (b) Curran, D. P. Synthesis 1988, 417 and 489. (c) Curran, D. P. In Comprehensive Organic Synthesis; Trost, B. M., Flamin, I., Semmelhack, M. F., Eds.; Pergmon Press: Oxford, UK, 1991; Vol. 4, pp 715 and 779. (d) Motherwell, W. B.; Crich, D. Free Radical Chain Reactions in Organic Synthesis; Academic Press: London, UK, 1992. (e) Fossey, J.; Lefort, D.; Sorba, J. Free Radical in Organic Chemistry; Wiley: New York, 1995.
    • (1992) Free Radical Chain Reactions in Organic Synthesis
    • Motherwell, W.B.1    Crich, D.2
  • 5
    • 0004125345 scopus 로고
    • Wiley: New York
    • For a general review and book, see: (a) Giese, B. Radical in Organic Synthesis: Formation of C- C Bonds; Pergmon Press: Oxford, UK, 1986. (b) Curran, D. P. Synthesis 1988, 417 and 489. (c) Curran, D. P. In Comprehensive Organic Synthesis; Trost, B. M., Flamin, I., Semmelhack, M. F., Eds.; Pergmon Press: Oxford, UK, 1991; Vol. 4, pp 715 and 779. (d) Motherwell, W. B.; Crich, D. Free Radical Chain Reactions in Organic Synthesis; Academic Press: London, UK, 1992. (e) Fossey, J.; Lefort, D.; Sorba, J. Free Radical in Organic Chemistry; Wiley: New York, 1995.
    • (1995) Free Radical in Organic Chemistry
    • Fossey, J.1    Lefort, D.2    Sorba, J.3
  • 24
    • 33845280764 scopus 로고
    • For the intramolecular radical carbon-carbon formation induced by a stoichiometric amount of reducing reagent, see: (a) Nugent, W. A.; RajanBabu, T. V. J. Am. Chem. Soc. 1988, 110, 8561. (b) Curran, D. P.; Totleben, M. J. J. Am. Chem. Soc. 1992, 114, 6050. (c) Hackmann, C.; Schäfer, H. J. Tetrahedron, 1993, 49, 4559. (d) Nakao, J.; Inoue, R.; Shinokubo, H.; Oshima, K. J. Org. Chem. 1997, 62, 1910. (e) Fujita, K.; Nakamura, T.; Yorimitsu, H.; Oshima, K. J. Am. Chem. Soc. 2001, 123, 3137. (f) Kita, Y.; Nambu, H.; Ramesh, N. G.; Anilkumar, G.; Matsugi, M. Org. Lett. 2001, 3, 1157. (g) Friestad, G. K. Tetrahedron 2001, 57, 5461.
    • (1988) J. Am. Chem. Soc. , vol.110 , pp. 8561
    • Nugent, W.A.1    RajanBabu, T.V.2
  • 25
    • 0009851507 scopus 로고
    • For the intramolecular radical carbon-carbon formation induced by a stoichiometric amount of reducing reagent, see: (a) Nugent, W. A.; RajanBabu, T. V. J. Am. Chem. Soc. 1988, 110, 8561. (b) Curran, D. P.; Totleben, M. J. J. Am. Chem. Soc. 1992, 114, 6050. (c) Hackmann, C.; Schäfer, H. J. Tetrahedron, 1993, 49, 4559. (d) Nakao, J.; Inoue, R.; Shinokubo, H.; Oshima, K. J. Org. Chem. 1997, 62, 1910. (e) Fujita, K.; Nakamura, T.; Yorimitsu, H.; Oshima, K. J. Am. Chem. Soc. 2001, 123, 3137. (f) Kita, Y.; Nambu, H.; Ramesh, N. G.; Anilkumar, G.; Matsugi, M. Org. Lett. 2001, 3, 1157. (g) Friestad, G. K. Tetrahedron 2001, 57, 5461.
    • (1992) J. Am. Chem. Soc. , vol.114 , pp. 6050
    • Curran, D.P.1    Totleben, M.J.2
  • 26
    • 0027276964 scopus 로고
    • For the intramolecular radical carbon-carbon formation induced by a stoichiometric amount of reducing reagent, see: (a) Nugent, W. A.; RajanBabu, T. V. J. Am. Chem. Soc. 1988, 110, 8561. (b) Curran, D. P.; Totleben, M. J. J. Am. Chem. Soc. 1992, 114, 6050. (c) Hackmann, C.; Schäfer, H. J. Tetrahedron, 1993, 49, 4559. (d) Nakao, J.; Inoue, R.; Shinokubo, H.; Oshima, K. J. Org. Chem. 1997, 62, 1910. (e) Fujita, K.; Nakamura, T.; Yorimitsu, H.; Oshima, K. J. Am. Chem. Soc. 2001, 123, 3137. (f) Kita, Y.; Nambu, H.; Ramesh, N. G.; Anilkumar, G.; Matsugi, M. Org. Lett. 2001, 3, 1157. (g) Friestad, G. K. Tetrahedron 2001, 57, 5461.
    • (1993) Tetrahedron , vol.49 , pp. 4559
    • Hackmann, C.1    Schäfer, H.J.2
  • 27
    • 0001535146 scopus 로고    scopus 로고
    • For the intramolecular radical carbon-carbon formation induced by a stoichiometric amount of reducing reagent, see: (a) Nugent, W. A.; RajanBabu, T. V. J. Am. Chem. Soc. 1988, 110, 8561. (b) Curran, D. P.; Totleben, M. J. J. Am. Chem. Soc. 1992, 114, 6050. (c) Hackmann, C.; Schäfer, H. J. Tetrahedron, 1993, 49, 4559. (d) Nakao, J.; Inoue, R.; Shinokubo, H.; Oshima, K. J. Org. Chem. 1997, 62, 1910. (e) Fujita, K.; Nakamura, T.; Yorimitsu, H.; Oshima, K. J. Am. Chem. Soc. 2001, 123, 3137. (f) Kita, Y.; Nambu, H.; Ramesh, N. G.; Anilkumar, G.; Matsugi, M. Org. Lett. 2001, 3, 1157. (g) Friestad, G. K. Tetrahedron 2001, 57, 5461.
    • (1997) J. Org. Chem. , vol.62 , pp. 1910
    • Nakao, J.1    Inoue, R.2    Shinokubo, H.3    Oshima, K.4
  • 28
    • 0034829548 scopus 로고    scopus 로고
    • For the intramolecular radical carbon-carbon formation induced by a stoichiometric amount of reducing reagent, see: (a) Nugent, W. A.; RajanBabu, T. V. J. Am. Chem. Soc. 1988, 110, 8561. (b) Curran, D. P.; Totleben, M. J. J. Am. Chem. Soc. 1992, 114, 6050. (c) Hackmann, C.; Schäfer, H. J. Tetrahedron, 1993, 49, 4559. (d) Nakao, J.; Inoue, R.; Shinokubo, H.; Oshima, K. J. Org. Chem. 1997, 62, 1910. (e) Fujita, K.; Nakamura, T.; Yorimitsu, H.; Oshima, K. J. Am. Chem. Soc. 2001, 123, 3137. (f) Kita, Y.; Nambu, H.; Ramesh, N. G.; Anilkumar, G.; Matsugi, M. Org. Lett. 2001, 3, 1157. (g) Friestad, G. K. Tetrahedron 2001, 57, 5461.
    • (2001) J. Am. Chem. Soc. , vol.123 , pp. 3137
    • Fujita, K.1    Nakamura, T.2    Yorimitsu, H.3    Oshima, K.4
  • 29
    • 0035912323 scopus 로고    scopus 로고
    • For the intramolecular radical carbon-carbon formation induced by a stoichiometric amount of reducing reagent, see: (a) Nugent, W. A.; RajanBabu, T. V. J. Am. Chem. Soc. 1988, 110, 8561. (b) Curran, D. P.; Totleben, M. J. J. Am. Chem. Soc. 1992, 114, 6050. (c) Hackmann, C.; Schäfer, H. J. Tetrahedron, 1993, 49, 4559. (d) Nakao, J.; Inoue, R.; Shinokubo, H.; Oshima, K. J. Org. Chem. 1997, 62, 1910. (e) Fujita, K.; Nakamura, T.; Yorimitsu, H.; Oshima, K. J. Am. Chem. Soc. 2001, 123, 3137. (f) Kita, Y.; Nambu, H.; Ramesh, N. G.; Anilkumar, G.; Matsugi, M. Org. Lett. 2001, 3, 1157. (g) Friestad, G. K. Tetrahedron 2001, 57, 5461.
    • (2001) Org. Lett. , vol.3 , pp. 1157
    • Kita, Y.1    Nambu, H.2    Ramesh, N.G.3    Anilkumar, G.4    Matsugi, M.5
  • 30
    • 0035948184 scopus 로고    scopus 로고
    • For the intramolecular radical carbon-carbon formation induced by a stoichiometric amount of reducing reagent, see: (a) Nugent, W. A.; RajanBabu, T. V. J. Am. Chem. Soc. 1988, 110, 8561. (b) Curran, D. P.; Totleben, M. J. J. Am. Chem. Soc. 1992, 114, 6050. (c) Hackmann, C.; Schäfer, H. J. Tetrahedron, 1993, 49, 4559. (d) Nakao, J.; Inoue, R.; Shinokubo, H.; Oshima, K. J. Org. Chem. 1997, 62, 1910. (e) Fujita, K.; Nakamura, T.; Yorimitsu, H.; Oshima, K. J. Am. Chem. Soc. 2001, 123, 3137. (f) Kita, Y.; Nambu, H.; Ramesh, N. G.; Anilkumar, G.; Matsugi, M. Org. Lett. 2001, 3, 1157. (g) Friestad, G. K. Tetrahedron 2001, 57, 5461.
    • (2001) Tetrahedron , vol.57 , pp. 5461
    • Friestad, G.K.1
  • 31
    • 0031973382 scopus 로고    scopus 로고
    • For the intramolecular radical carbon-carbon formation induced by a catalytic amount of reducing reagent, see: (a) Hayashi, Y.; Shinokubo, H.; Oshima, K. Tetrahedron Lett. 1998, 39, 63. (b) Wakabayashi, K.; Yorimitsu, H.; Oshima, K. J. Am. Chem. Soc. 2001, 123, 5374.
    • (1998) Tetrahedron Lett. , vol.39 , pp. 63
    • Hayashi, Y.1    Shinokubo, H.2    Oshima, K.3
  • 32
    • 0034801334 scopus 로고    scopus 로고
    • For the intramolecular radical carbon-carbon formation induced by a catalytic amount of reducing reagent, see: (a) Hayashi, Y.; Shinokubo, H.; Oshima, K. Tetrahedron Lett. 1998, 39, 63. (b) Wakabayashi, K.; Yorimitsu, H.; Oshima, K. J. Am. Chem. Soc. 2001, 123, 5374.
    • (2001) J. Am. Chem. Soc. , vol.123 , pp. 5374
    • Wakabayashi, K.1    Yorimitsu, H.2    Oshima, K.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.