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Volumn 45, Issue 32, 2006, Pages 5364-5368

Synthesis of highly substituted N-hydroxyindoles through 1,5-Addition of carbon nucleophiles to in situ generated unsaturated nitrones

Author keywords

N hydroxyindoles; Nitrogen heterocycles; Silanes; Stannanes; Synthetic methods

Indexed keywords

N-HYDROXYINDOLES; NITROGEN HETEROCYCLES; STANNANES; SYNTHETIC METHODS;

EID: 33747893097     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200601808     Document Type: Article
Times cited : (42)

References (23)
  • 2
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    • Angew. Chem. Int. Ed. 2005, 44, 3736-3740.
    • (2005) Angew. Chem. Int. Ed. , vol.44 , pp. 3736-3740
  • 7
    • 2242456130 scopus 로고    scopus 로고
    • [Chem. Abstr. 2000, 132, 121531];
    • (2000) Chem. Abstr. , vol.132 , pp. 121531
  • 9
    • 0036096658 scopus 로고    scopus 로고
    • For selected reviews on N-hydroxyindoles and their derivatives, see: a) M. Somei, Adv. Heterocycl. Chem. 2002, 82, 101-155;
    • (2002) Adv. Heterocycl. Chem. , vol.82 , pp. 101-155
    • Somei, M.1
  • 10
    • 0033117650 scopus 로고    scopus 로고
    • b) M. Somei, Heterocycles 1999, 50, 1157-1211;
    • (1999) Heterocycles , vol.50 , pp. 1157-1211
    • Somei, M.1
  • 19
    • 33747893979 scopus 로고    scopus 로고
    • note
    • This type of reaction is sometimes referred to as a 1,4-addition.
  • 20
    • 18744403152 scopus 로고    scopus 로고
    • Ed.: A. Padwa, Thieme, New York
    • For a comprehensive review on nitrones, see: P. Merino, Science of Synthesis, Vol. 27 (Ed.: A. Padwa), Thieme, New York, 2004, pp. 511-580.
    • (2004) Science of Synthesis , vol.27 , pp. 511-580
    • Merino, P.1
  • 21
    • 33747875644 scopus 로고    scopus 로고
    • CCDC 603155 (19) and 603156 (23) contain the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/ data_request/cif.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.