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Volumn 22, Issue 24, 2003, Pages 4836-4838

Synthesis and Catalytic Characteristics of Novel Constrained-Geometry Organoactinide Catalysts. The First Example of Actiniae-Mediated Intramolecular Hydroamination

Author keywords

[No Author keywords available]

Indexed keywords

CYCLIZATION; INTRAMOLECULAR HYDROAMINATION;

EID: 0345016345     PISSN: 02767333     EISSN: None     Source Type: Journal    
DOI: 10.1021/om034093f     Document Type: Article
Times cited : (113)

References (48)
  • 1
    • 0041711028 scopus 로고    scopus 로고
    • For recent hydroamination reviews see: (a) Pohlki, F.; Doye, S. Chem. Soc. Rev. 2003, 32 (2), 104-114.
    • (2003) Chem. Soc. Rev. , vol.32 , Issue.2 , pp. 104-114
    • Pohlki, F.1    Doye, S.2
  • 18
    • 0141577873 scopus 로고    scopus 로고
    • For CGC reviews, see: (a) Okuda, J. Dalton Trans. 2003, 2367-2378.
    • (2003) Dalton Trans. , pp. 2367-2378
    • Okuda, J.1
  • 19
    • 0036625218 scopus 로고    scopus 로고
    • (b) Arndt, S.; Okuda, J. Chem. Rev. 2002, 102 (6), 1953-1976.
    • (2002) Chem. Rev. , vol.102 , Issue.6 , pp. 1953-1976
    • Arndt, S.1    Okuda, J.2
  • 27
    • 0000969532 scopus 로고
    • Abel, E. W., Stone, F. G. A., Wilkinson, G., Eds.; Pergamon: New York
    • (a) Edelmann, F. T. In Comprehensive Organometallic Chemistry II; Abel, E. W., Stone, F. G. A., Wilkinson, G., Eds.; Pergamon: New York, 1995; Vol. 4, pp 11-213.
    • (1995) Comprehensive Organometallic Chemistry II , vol.4 , pp. 11-213
    • Edelmann, F.T.1
  • 29
    • 84942812532 scopus 로고
    • Abel, E. W., Stone, F. G. A., Wilkinson, G., Eds.; Pergamon: New York
    • (c) Marks, T. J.; Ernst, R. D. In Comprehensive Organometallic Chemistry; Abel, E. W., Stone, F. G. A., Wilkinson, G., Eds.; Pergamon: New York, 1982; Vol. 3, pp 173-270.
    • (1982) Comprehensive Organometallic Chemistry , vol.3 , pp. 173-270
    • Marks, T.J.1    Ernst, R.D.2
  • 30
    • 0345273521 scopus 로고    scopus 로고
    • Communicated in part at ISHHC-XI, July 21-25, 2003, Evanston, IL, Poster Abstract No. 034
    • Communicated in part at ISHHC-XI, July 21-25, 2003, Evanston, IL, Poster Abstract No. 034.
  • 38
    • 0344842108 scopus 로고    scopus 로고
    • See Supporting Information for complete details
    • See Supporting Information for complete details.
  • 41
    • 0345273520 scopus 로고    scopus 로고
    • note
    • Single crystals suitable for X-ray diffraction studies have not been obtained to date, although NMR spectroscopy, electron-impact mass spectrometry, and elemental analysis indicate clean formation of 3 and 4 by this method.
  • 47
    • 0035956453 scopus 로고    scopus 로고
    • and references therein
    • For previously reported studies of organoactinide-mediated intermolecular terminal alkyne hydroamination, see: Straub, T.; Haskel, A.; Neyroud, T. G.; Kapon, M.; Botoshansky, M.; Eisen, M. S. Organometallics 2001, 20 (24), 5017-5035, and references therein.
    • (2001) Organometallics , vol.20 , Issue.24 , pp. 5017-5035
    • Straub, T.1    Haskel, A.2    Neyroud, T.G.3    Kapon, M.4    Botoshansky, M.5    Eisen, M.S.6
  • 48
    • 0344842107 scopus 로고    scopus 로고
    • note
    • An alternative cycle proceeding through an An=NR species (see ref 18) as a catalytically inactive species or as the active catalyst species cannot be rigorously ruled out at this time. Imide formation as a reversible, turnover-limiting step seems unlikely given the observed independence of overall rate on [substrate].


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.