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Volumn , Issue 3, 2011, Pages 455-457

Acid-catalyzed [3,3] sigmatropic rearrangement of N-Cbz-diaryl hydrazide for the synthesis of mono-N-Cbz-1,1′-biaryl-2,2′-diamine

Author keywords

Amines; Biaryls; Cross coupling; Hydrazides; Sigmatropic rearrangement

Indexed keywords


EID: 78651269096     PISSN: 1434193X     EISSN: 10990690     Source Type: Journal    
DOI: 10.1002/ejoc.201001461     Document Type: Article
Times cited : (18)

References (47)
  • 1
    • 78651312114 scopus 로고    scopus 로고
    • For recent reviews on biaryls, see
    • For recent reviews on biaryls, see
  • 11
    • 0000718373 scopus 로고    scopus 로고
    • L. Pu, Chem. Rev. 1998, 98, 2405.
    • (1998) Chem. Rev. , vol.98 , pp. 2405
    • Pu, L.1
  • 30
    • 78651333193 scopus 로고    scopus 로고
    • The first Pd-catalyzed coupling reaction of hydrazine (en route to aryl hydrazine) has been recently reported.
    • The first Pd-catalyzed coupling reaction of hydrazine (en route to aryl hydrazine) has been recently reported., R. J. Lundgren, M. Stradiotto, Angew. Chem. Int. Ed. 2010, 49, 2.
    • (2010) Angew. Chem. Int. Ed. , vol.49 , pp. 2
    • Lundgren, R.J.1    Stradiotto, M.2
  • 44
    • 78651269842 scopus 로고    scopus 로고
    • The Fischer indolization reactions of electron-deficient aryl hydrazines are often less efficient than those of electron-rich aryl hydrazines
    • The Fischer indolization reactions of electron-deficient aryl hydrazines are often less efficient than those of electron-rich aryl hydrazines


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.