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Volumn , Issue 9, 2004, Pages 1359-1362

Facile one-pot synthesis of di- and tri-substituted furans from acyl isocyanates using trimethylsilyldiazomethane

Author keywords

Acyl isocyanates; Diels Alder reaction; Furans; Oxazoles; Trimethylsilyldiazomethane

Indexed keywords

ACYLATION; ESTERS; IN SITU PROCESSING; REACTION KINETICS; SYNTHESIS (CHEMICAL);

EID: 3042829623     PISSN: 00397881     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2004-822397     Document Type: Article
Times cited : (12)

References (23)
  • 14
    • 0009790123 scopus 로고    scopus 로고
    • Fleming, I., Ed.; Georg Thieme Verlag: Stuttgart
    • Reviews: (a) Shioiri, T.; Aoyama, T. Science of Synthesis, Vol. 4; Fleming, I., Ed.; Georg Thieme Verlag: Stuttgart, 2002, 569. (b) Shioiri, T.; Aoyama, T. J. Synth. Org. Chem., Jpn. 1996, 54, 918. (c) Shioiri, T.; Aoyama, T. Advances in the Use of Synthons in Organic Chemistry, Vol. 1; Dondoni, A., Ed.; JAI Press Ltd.: London, 1993, 51.
    • (2002) Science of Synthesis , vol.4 , pp. 569
    • Shioiri, T.1    Aoyama, T.2
  • 15
    • 0030289032 scopus 로고    scopus 로고
    • Reviews: (a) Shioiri, T.; Aoyama, T. Science of Synthesis, Vol. 4; Fleming, I., Ed.; Georg Thieme Verlag: Stuttgart, 2002, 569. (b) Shioiri, T.; Aoyama, T. J. Synth. Org. Chem., Jpn. 1996, 54, 918. (c) Shioiri, T.; Aoyama, T. Advances in the Use of Synthons in Organic Chemistry, Vol. 1; Dondoni, A., Ed.; JAI Press Ltd.: London, 1993, 51.
    • (1996) J. Synth. Org. Chem., Jpn. , vol.54 , pp. 918
    • Shioiri, T.1    Aoyama, T.2
  • 16
    • 0002623376 scopus 로고
    • Dondoni, A., Ed.; JAI Press Ltd.: London
    • Reviews: (a) Shioiri, T.; Aoyama, T. Science of Synthesis, Vol. 4; Fleming, I., Ed.; Georg Thieme Verlag: Stuttgart, 2002, 569. (b) Shioiri, T.; Aoyama, T. J. Synth. Org. Chem., Jpn. 1996, 54, 918. (c) Shioiri, T.; Aoyama, T. Advances in the Use of Synthons in Organic Chemistry, Vol. 1; Dondoni, A., Ed.; JAI Press Ltd.: London, 1993, 51.
    • (1993) Advances in the Use of Synthons in Organic Chemistry , vol.1 , pp. 51
    • Shioiri, T.1    Aoyama, T.2
  • 17
    • 0842326654 scopus 로고    scopus 로고
    • Recent reports: (a) Shoji, Y.; Hari, Y.; Aoyama, T. Tetrahedron Lett. 2004, 45, 1769. (b) Hari, Y.; Tanaka, S.; Takuma, Y.; Aoyama, T. Synlett 2003, 2151. (c) Miyabe, R.; Shioiri, T.; Aoyama, T. Heterocycles 2002, 57, 1313.
    • (2004) Tetrahedron Lett. , vol.45 , pp. 1769
    • Shoji, Y.1    Hari, Y.2    Aoyama, T.3
  • 18
    • 0242408241 scopus 로고    scopus 로고
    • Recent reports: (a) Shoji, Y.; Hari, Y.; Aoyama, T. Tetrahedron Lett. 2004, 45, 1769. (b) Hari, Y.; Tanaka, S.; Takuma, Y.; Aoyama, T. Synlett 2003, 2151. (c) Miyabe, R.; Shioiri, T.; Aoyama, T. Heterocycles 2002, 57, 1313.
    • (2003) Synlett , pp. 2151
    • Hari, Y.1    Tanaka, S.2    Takuma, Y.3    Aoyama, T.4
  • 19
    • 0036645812 scopus 로고    scopus 로고
    • Recent reports: (a) Shoji, Y.; Hari, Y.; Aoyama, T. Tetrahedron Lett. 2004, 45, 1769. (b) Hari, Y.; Tanaka, S.; Takuma, Y.; Aoyama, T. Synlett 2003, 2151. (c) Miyabe, R.; Shioiri, T.; Aoyama, T. Heterocycles 2002, 57, 1313.
    • (2002) Heterocycles , vol.57 , pp. 1313
    • Miyabe, R.1    Shioiri, T.2    Aoyama, T.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.