메뉴 건너뛰기




Volumn 63, Issue 19, 1998, Pages 6535-6545

An Intramolecular Allenic [2 + 2 + 1] Cycloaddition

Author keywords

[No Author keywords available]

Indexed keywords


EID: 0001161843     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo980548c     Document Type: Article
Times cited : (89)

References (28)
  • 2
    • 0001334715 scopus 로고
    • Trost, B. M., Ed.; Pergamon: Oxford
    • Schore, N. E. In Comprehensive Organic Synthesis; Trost, B. M., Ed.; Pergamon: Oxford, 1991; Vol. 5, p 1037.
    • (1991) Comprehensive Organic Synthesis , vol.5 , pp. 1037
    • Schore, N.E.1
  • 3
    • 0028936564 scopus 로고
    • Kent, J. L.; Wan, H.; Brummond, K. M. Tetrahedron Lett. 1995, 36, 2407. Brummond, K. M.; Wan, H. Tetrahedron Lett. 1998, 39, 931. Since the initial report by ourselves other groups have reported [2 + 2 + 1] cycloadditions with alkynyl allenes. (a) Ahmar, M.; Antras, F.; Cazes, B. Tetrahedron Lett. 1995, 36, 4417-4420. (b) Ahmar, M.; Locatelli, C.; Colombier, D.; Cazes, B. Tetrahedron Lett. 1997, 38, 5281-5284. (c) Hicks, F. A.; Kablaoui, N. M.; Buchwald, S. L. J. Am. Chem. Soc. 1996, 118, 9450-9451.
    • (1995) Tetrahedron Lett. , vol.36 , pp. 2407
    • Kent, J.L.1    Wan, H.2    Brummond, K.M.3
  • 4
    • 0032568050 scopus 로고    scopus 로고
    • Kent, J. L.; Wan, H.; Brummond, K. M. Tetrahedron Lett. 1995, 36, 2407. Brummond, K. M.; Wan, H. Tetrahedron Lett. 1998, 39, 931. Since the initial report by ourselves other groups have reported [2 + 2 + 1] cycloadditions with alkynyl allenes. (a) Ahmar, M.; Antras, F.; Cazes, B. Tetrahedron Lett. 1995, 36, 4417-4420. (b) Ahmar, M.; Locatelli, C.; Colombier, D.; Cazes, B. Tetrahedron Lett. 1997, 38, 5281-5284. (c) Hicks, F. A.; Kablaoui, N. M.; Buchwald, S. L. J. Am. Chem. Soc. 1996, 118, 9450-9451.
    • (1998) Tetrahedron Lett. , vol.39 , pp. 931
    • Brummond, K.M.1    Wan, H.2
  • 5
    • 0029003734 scopus 로고
    • Kent, J. L.; Wan, H.; Brummond, K. M. Tetrahedron Lett. 1995, 36, 2407. Brummond, K. M.; Wan, H. Tetrahedron Lett. 1998, 39, 931. Since the initial report by ourselves other groups have reported [2 + 2 + 1] cycloadditions with alkynyl allenes. (a) Ahmar, M.; Antras, F.; Cazes, B. Tetrahedron Lett. 1995, 36, 4417-4420. (b) Ahmar, M.; Locatelli, C.; Colombier, D.; Cazes, B. Tetrahedron Lett. 1997, 38, 5281-5284. (c) Hicks, F. A.; Kablaoui, N. M.; Buchwald, S. L. J. Am. Chem. Soc. 1996, 118, 9450-9451.
    • (1995) Tetrahedron Lett. , vol.36 , pp. 4417-4420
    • Ahmar, M.1    Antras, F.2    Cazes, B.3
  • 6
    • 0030805614 scopus 로고    scopus 로고
    • Kent, J. L.; Wan, H.; Brummond, K. M. Tetrahedron Lett. 1995, 36, 2407. Brummond, K. M.; Wan, H. Tetrahedron Lett. 1998, 39, 931. Since the initial report by ourselves other groups have reported [2 + 2 + 1] cycloadditions with alkynyl allenes. (a) Ahmar, M.; Antras, F.; Cazes, B. Tetrahedron Lett. 1995, 36, 4417-4420. (b) Ahmar, M.; Locatelli, C.; Colombier, D.; Cazes, B. Tetrahedron Lett. 1997, 38, 5281-5284. (c) Hicks, F. A.; Kablaoui, N. M.; Buchwald, S. L. J. Am. Chem. Soc. 1996, 118, 9450-9451.
    • (1997) Tetrahedron Lett. , vol.38 , pp. 5281-5284
    • Ahmar, M.1    Locatelli, C.2    Colombier, D.3    Cazes, B.4
  • 7
    • 0029952824 scopus 로고    scopus 로고
    • Kent, J. L.; Wan, H.; Brummond, K. M. Tetrahedron Lett. 1995, 36, 2407. Brummond, K. M.; Wan, H. Tetrahedron Lett. 1998, 39, 931. Since the initial report by ourselves other groups have reported [2 + 2 + 1] cycloadditions with alkynyl allenes. (a) Ahmar, M.; Antras, F.; Cazes, B. Tetrahedron Lett. 1995, 36, 4417-4420. (b) Ahmar, M.; Locatelli, C.; Colombier, D.; Cazes, B. Tetrahedron Lett. 1997, 38, 5281-5284. (c) Hicks, F. A.; Kablaoui, N. M.; Buchwald, S. L. J. Am. Chem. Soc. 1996, 118, 9450-9451.
    • (1996) J. Am. Chem. Soc. , vol.118 , pp. 9450-9451
    • Hicks, F.A.1    Kablaoui, N.M.2    Buchwald, S.L.3
  • 10
    • 0029294531 scopus 로고
    • Forman, B. M.; Tontonoz, P.; Chen, J.; Brun, R. P.; Spiegelman, B. M.; Evans, R. M. Cell, 1995, 83, 803-812. Wahli, W.; Braissant, O.; Desvergne, B. Chem. Biol. 1995, 2, 261. Turner, N. C. Drug Discovery Today 1996, 1, 109.
    • (1995) Chem. Biol. , vol.2 , pp. 261
    • Wahli, W.1    Braissant, O.2    Desvergne, B.3
  • 11
    • 0000673973 scopus 로고    scopus 로고
    • Forman, B. M.; Tontonoz, P.; Chen, J.; Brun, R. P.; Spiegelman, B. M.; Evans, R. M. Cell, 1995, 83, 803-812. Wahli, W.; Braissant, O.; Desvergne, B. Chem. Biol. 1995, 2, 261. Turner, N. C. Drug Discovery Today 1996, 1, 109.
    • (1996) Drug Discovery Today , vol.1 , pp. 109
    • Turner, N.C.1
  • 12
    • 85034479547 scopus 로고    scopus 로고
    • For the monosubstituted allenes complexation of the alkynes with dicobalt octacarbonyl could be effected, but attempts to promote cyclization resulted in decompostion or recovery of starting material
    • For the monosubstituted allenes complexation of the alkynes with dicobalt octacarbonyl could be effected, but attempts to promote cyclization resulted in decompostion or recovery of starting material.
  • 14
    • 85034474524 scopus 로고    scopus 로고
    • note
    • 6 (1.5 equiv) and DMSO (10 equiv) in toluene at 110°C.
  • 28
    • 0001116565 scopus 로고
    • Mikami, K.; Yoshida, A.; Matsumoto, S.; Feng, F.; Matsumoto, Y.; Sugino, A.; Hanamoto, T.; Inanaga, J. Tetrahedron Lett. 1995, 36, 907. Tabuchi, T.; Inanaga, J.; Yamaguchi, M. Tetrahedron Lett. 1986, 27, 5237.
    • (1986) Tetrahedron Lett. , vol.27 , pp. 5237
    • Tabuchi, T.1    Inanaga, J.2    Yamaguchi, M.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.