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Volumn 45, Issue 46, 2006, Pages 7838-7842

General preparation of primary, secondary, and tertiary aryl amines by the oxidative coupling of polyfunctional aryl and heteroaryl amidocuprates

Author keywords

Amination; Amines; C N bond formation; Cuprates; Grignard reagents

Indexed keywords

AMINATION; CHEMICAL BONDS; COPPER COMPOUNDS; MAGNESIUM COMPOUNDS; OXIDATION; STEREOCHEMISTRY;

EID: 33845303550     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200603089     Document Type: Article
Times cited : (71)

References (62)
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    • and references therein
    • b) J. G. de Vries, Can. J. Chem. 2001, 79, 1086, and references therein;
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    • c) applications in the preparation of biologically active compounds: M. Prashad, Top. Organomet. Chem. 2004, 6, 181;
    • (2004) Top. Organomet. Chem. , vol.6 , pp. 181
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    • For selected reviews, see
    • For selected reviews, see: a) J. F. Hartwig, Angew. Chem. 1998, 110, 2154;
    • (1998) Angew. Chem. , vol.110 , pp. 2154
    • Hartwig, J.F.1
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    • 0042704188 scopus 로고    scopus 로고
    • The reaction between ortho-substituted aryl halides and LiHMDS generally fails to form C-N bonds because of the steric hindrance of the two bulky silyl groups; for a discussion, see: a) S. Lee, M. Jørgensen, J. F. Hartwig, Org. Lett. 2001, 3, 2729;
    • (2001) Org. Lett. , vol.3 , pp. 2729
    • Lee, S.1    Jørgensen, M.2    Hartwig, J.F.3
  • 48
  • 57
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    • note
    • See the Supporting Information.
  • 62
    • 33845285502 scopus 로고    scopus 로고
    • note
    • The corresponding secondary amine was obtained in 96% yield upon deprotection.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.