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Volumn , Issue 13, 1999, Pages 1217-1218

Synthesis and domino reactions of 1,1-bis(hydroxymethyl)allenes

Author keywords

[No Author keywords available]

Indexed keywords

ALKYL ARYL KETONE; ALLENE DERIVATIVE; HYDROXIDE; POLYCYCLIC AROMATIC HYDROCARBON;

EID: 0033532845     PISSN: 13597345     EISSN: None     Source Type: Journal    
DOI: 10.1039/a901208g     Document Type: Article
Times cited : (22)

References (18)
  • 1
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    • For reviews of domino reactions, see: L. F. Tietze and U. Beifuss, Angew. Chem., Int. Ed. Engl., 1993, 32, 131; A. de Meijere and F. E. Meyer, Angew. Chem., Int. Ed. Engl., 1994, 33, 2379.
    • (1993) Angew. Chem., Int. Ed. Engl. , vol.32 , pp. 131
    • Tietze, L.F.1    Beifuss, U.2
  • 2
    • 33748647785 scopus 로고
    • For reviews of domino reactions, see: L. F. Tietze and U. Beifuss, Angew. Chem., Int. Ed. Engl., 1993, 32, 131; A. de Meijere and F. E. Meyer, Angew. Chem., Int. Ed. Engl., 1994, 33, 2379.
    • (1994) Angew. Chem., Int. Ed. Engl. , vol.33 , pp. 2379
    • De Meijere, A.1    Meyer, F.E.2
  • 3
    • 33746372903 scopus 로고
    • H. Hopf and G. Maas, Angew. Chem., Int. Ed. Engl., 1992, 31, 931; F. Toda, K. Tanaka, I. Sano and T. Isozaki, Angew. Chem., Int. Ed. Engl., 1994, 33, 1757; H. Hopf, P. G. Jones, P. Bubenitschek and C. Werner, Angew. Chem., Int. Ed. Engl., 1995, 34, 2367.
    • (1992) Angew. Chem., Int. Ed. Engl. , vol.31 , pp. 931
    • Hopf, H.1    Maas, G.2
  • 4
    • 33748222588 scopus 로고
    • H. Hopf and G. Maas, Angew. Chem., Int. Ed. Engl., 1992, 31, 931; F. Toda, K. Tanaka, I. Sano and T. Isozaki, Angew. Chem., Int. Ed. Engl., 1994, 33, 1757; H. Hopf, P. G. Jones, P. Bubenitschek and C. Werner, Angew. Chem., Int. Ed. Engl., 1995, 34, 2367.
    • (1994) Angew. Chem., Int. Ed. Engl. , vol.33 , pp. 1757
    • Toda, F.1    Tanaka, K.2    Sano, I.3    Isozaki, T.4
  • 5
    • 33750436741 scopus 로고
    • H. Hopf and G. Maas, Angew. Chem., Int. Ed. Engl., 1992, 31, 931; F. Toda, K. Tanaka, I. Sano and T. Isozaki, Angew. Chem., Int. Ed. Engl., 1994, 33, 1757; H. Hopf, P. G. Jones, P. Bubenitschek and C. Werner, Angew. Chem., Int. Ed. Engl., 1995, 34, 2367.
    • (1995) Angew. Chem., Int. Ed. Engl. , vol.34 , pp. 2367
    • Hopf, H.1    Jones, P.G.2    Bubenitschek, P.3    Werner, C.4
  • 6
    • 0029026345 scopus 로고
    • S. Blechert, R. Knier, H. Schroers andT. Wirth, Synthesis 1995, 592; R. Grigg, V. Loganathan, V. Sridharan, P. Stevenson, S. Sukirthalingam and T. Worakun, Tetrahedron, 1996, 52, 11 479; M. Schmittel, M. Strittmatter and S. Kiau, Angew. Chem., Int. Ed. Engl., 1996, 35, 1843; T. Doi, A. Yanagisawa, S. Nakanishi, K. Yamamoto and T. Takahashi, J. Org. Chem., 1996, 61, 2602; H. Nemoto, M. Yoshida and K. Fukumoto, J. Org. Chem., 1997, 62, 6450.
    • (1995) Synthesis , pp. 592
    • Blechert, S.1    Knier, R.2    Schroers, H.3    Wirth, T.4
  • 7
    • 0030603132 scopus 로고    scopus 로고
    • S. Blechert, R. Knier, H. Schroers andT. Wirth, Synthesis 1995, 592; R. Grigg, V. Loganathan, V. Sridharan, P. Stevenson, S. Sukirthalingam and T. Worakun, Tetrahedron, 1996, 52, 11 479; M. Schmittel, M. Strittmatter and S. Kiau, Angew. Chem., Int. Ed. Engl., 1996, 35, 1843; T. Doi, A. Yanagisawa, S. Nakanishi, K. Yamamoto and T. Takahashi, J. Org. Chem., 1996, 61, 2602; H. Nemoto, M. Yoshida and K. Fukumoto, J. Org. Chem., 1997, 62, 6450.
    • (1996) Tetrahedron , vol.52 , pp. 11479
    • Grigg, R.1    Loganathan, V.2    Sridharan, V.3    Stevenson, P.4    Sukirthalingam, S.5    Worakun, T.6
  • 8
    • 0030515269 scopus 로고    scopus 로고
    • S. Blechert, R. Knier, H. Schroers andT. Wirth, Synthesis 1995, 592; R. Grigg, V. Loganathan, V. Sridharan, P. Stevenson, S. Sukirthalingam and T. Worakun, Tetrahedron, 1996, 52, 11 479; M. Schmittel, M. Strittmatter and S. Kiau, Angew. Chem., Int. Ed. Engl., 1996, 35, 1843; T. Doi, A. Yanagisawa, S. Nakanishi, K. Yamamoto and T. Takahashi, J. Org. Chem., 1996, 61, 2602; H. Nemoto, M. Yoshida and K. Fukumoto, J. Org. Chem., 1997, 62, 6450.
    • (1996) Angew. Chem., Int. Ed. Engl. , vol.35 , pp. 1843
    • Schmittel, M.1    Strittmatter, M.2    Kiau, S.3
  • 9
    • 0000810091 scopus 로고    scopus 로고
    • S. Blechert, R. Knier, H. Schroers andT. Wirth, Synthesis 1995, 592; R. Grigg, V. Loganathan, V. Sridharan, P. Stevenson, S. Sukirthalingam and T. Worakun, Tetrahedron, 1996, 52, 11 479; M. Schmittel, M. Strittmatter and S. Kiau, Angew. Chem., Int. Ed. Engl., 1996, 35, 1843; T. Doi, A. Yanagisawa, S. Nakanishi, K. Yamamoto and T. Takahashi, J. Org. Chem., 1996, 61, 2602; H. Nemoto, M. Yoshida and K. Fukumoto, J. Org. Chem., 1997, 62, 6450.
    • (1996) J. Org. Chem. , vol.61 , pp. 2602
    • Doi, T.1    Yanagisawa, A.2    Nakanishi, S.3    Yamamoto, K.4    Takahashi, T.5
  • 10
    • 0000018950 scopus 로고    scopus 로고
    • S. Blechert, R. Knier, H. Schroers andT. Wirth, Synthesis 1995, 592; R. Grigg, V. Loganathan, V. Sridharan, P. Stevenson, S. Sukirthalingam and T. Worakun, Tetrahedron, 1996, 52, 11 479; M. Schmittel, M. Strittmatter and S. Kiau, Angew. Chem., Int. Ed. Engl., 1996, 35, 1843; T. Doi, A. Yanagisawa, S. Nakanishi, K. Yamamoto and T. Takahashi, J. Org. Chem., 1996, 61, 2602; H. Nemoto, M. Yoshida and K. Fukumoto, J. Org. Chem., 1997, 62, 6450.
    • (1997) J. Org. Chem. , vol.62 , pp. 6450
    • Nemoto, H.1    Yoshida, M.2    Fukumoto, K.3
  • 11
    • 0002993021 scopus 로고    scopus 로고
    • A 1,1-bis(hydroxymethyl)allene has been previously prepared by a different route in 17% yield: H. Mori, K. Ikoma and S. Katsumura, Chem. Commun., 1997, 2243.
    • (1997) Chem. Commun. , pp. 2243
    • Mori, H.1    Ikoma, K.2    Katsumura, S.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.