메뉴 건너뛰기




Volumn 5, Issue 19, 2003, Pages 3479-3481

Titanocene-Catalyzed Regioselective syn-Hydrosilation of Alkynes

Author keywords

[No Author keywords available]

Indexed keywords

ALKYNE DERIVATIVE; BUTYLLITHIUM; LITHIUM DERIVATIVE; TITANOCENE; UNCLASSIFIED DRUG;

EID: 0344824438     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol035277t     Document Type: Article
Times cited : (54)

References (40)
  • 4
    • 84988124945 scopus 로고
    • For application of alkenylsilanes to palladium-catalyzed cross-coupling reactions, see: (a) Hatanaka, Y.; Hiyama, T. Synlett 1991, 845. (b) Hiyama, T. Organosilicon Compounds in Cross-Coupling Reactions. In Metal-Catalyzed Cross-Coupling Reactions; Diederich, F., Stang, P., Eds.; Wiley-VCH: Weinheim, 1998.
    • (1991) Synlett , pp. 845
    • Hatanaka, Y.1    Hiyama, T.2
  • 5
    • 0000390817 scopus 로고    scopus 로고
    • Organosilicon compounds in cross-coupling reactions
    • Diederich, F., Stang, P., Eds.; Wiley-VCH: Weinheim
    • For application of alkenylsilanes to palladium-catalyzed cross-coupling reactions, see: (a) Hatanaka, Y.; Hiyama, T. Synlett 1991, 845. (b) Hiyama, T. Organosilicon Compounds in Cross-Coupling Reactions. In Metal-Catalyzed Cross-Coupling Reactions; Diederich, F., Stang, P., Eds.; Wiley-VCH: Weinheim, 1998.
    • (1998) Metal-Catalyzed Cross-Coupling Reactions
    • Hiyama, T.1
  • 6
    • 0036172664 scopus 로고    scopus 로고
    • For application of alkenylsilanes to rhodium-catalyzed nucleophilic addition reactions, see: (a) Fujii, T.; Koike, T.; Mori, A.; Osakada, K. Synlett 2002, 295. (b) Fujii, T.; Koike, T.; Mori, A.; Osakada, K. Synlett 2002, 298. (c) Oi, S.; Honma, Y.; Inoue, Y. Org. Lett. 2002, 4, 667. (d) Oi, S.; Taira, A.; Honma, Y.; Inoue, Y. Org. Lett. 2003, 5, 97.
    • (2002) Synlett , pp. 295
    • Fujii, T.1    Koike, T.2    Mori, A.3    Osakada, K.4
  • 7
    • 0036170255 scopus 로고    scopus 로고
    • For application of alkenylsilanes to rhodium-catalyzed nucleophilic addition reactions, see: (a) Fujii, T.; Koike, T.; Mori, A.; Osakada, K. Synlett 2002, 295. (b) Fujii, T.; Koike, T.; Mori, A.; Osakada, K. Synlett 2002, 298. (c) Oi, S.; Honma, Y.; Inoue, Y. Org. Lett. 2002, 4, 667. (d) Oi, S.; Taira, A.; Honma, Y.; Inoue, Y. Org. Lett. 2003, 5, 97.
    • (2002) Synlett , pp. 298
    • Fujii, T.1    Koike, T.2    Mori, A.3    Osakada, K.4
  • 8
    • 0000796405 scopus 로고    scopus 로고
    • For application of alkenylsilanes to rhodium-catalyzed nucleophilic addition reactions, see: (a) Fujii, T.; Koike, T.; Mori, A.; Osakada, K. Synlett 2002, 295. (b) Fujii, T.; Koike, T.; Mori, A.; Osakada, K. Synlett 2002, 298. (c) Oi, S.; Honma, Y.; Inoue, Y. Org. Lett. 2002, 4, 667. (d) Oi, S.; Taira, A.; Honma, Y.; Inoue, Y. Org. Lett. 2003, 5, 97.
    • (2002) Org. Lett. , vol.4 , pp. 667
    • Oi, S.1    Honma, Y.2    Inoue, Y.3
  • 9
    • 0037647172 scopus 로고    scopus 로고
    • For application of alkenylsilanes to rhodium-catalyzed nucleophilic addition reactions, see: (a) Fujii, T.; Koike, T.; Mori, A.; Osakada, K. Synlett 2002, 295. (b) Fujii, T.; Koike, T.; Mori, A.; Osakada, K. Synlett 2002, 298. (c) Oi, S.; Honma, Y.; Inoue, Y. Org. Lett. 2002, 4, 667. (d) Oi, S.; Taira, A.; Honma, Y.; Inoue, Y. Org. Lett. 2003, 5, 97.
    • (2003) Org. Lett. , vol.5 , pp. 97
    • Oi, S.1    Taira, A.2    Honma, Y.3    Inoue, Y.4
  • 10
    • 0000829913 scopus 로고
    • Patai, S., Rappoport, Z., Eds.; John Wiley: Chichester
    • (a) Ojima, I. In The Chemistry of Organic Silicon Compounds; Patai, S., Rappoport, Z., Eds.; John Wiley: Chichester, 1989; p 1479.
    • (1989) The Chemistry of Organic Silicon Compounds , pp. 1479
    • Ojima, I.1
  • 11
    • 0000487195 scopus 로고
    • Trost, B. M., Fleming, I., Eds.; Pergamon Press: Oxford
    • (b) Hiyama, T.; Kusumoto, T. In Comprehensive Organic Synthesis; Trost, B. M., Fleming, I., Eds.; Pergamon Press: Oxford, 1991; Vol. 8, p 763.
    • (1991) Comprehensive Organic Synthesis , vol.8 , pp. 763
    • Hiyama, T.1    Kusumoto, T.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.