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Volumn 352, Issue 14-15, 2010, Pages 2459-2462

A two-step synthesis of unsymmetrical 1,4-disubstituted carbazoles from sulfonylindoles under heterogeneous catalysis

Author keywords

carbazoles; electrophilic substitution; heterogeneous catalysis; nitro compounds

Indexed keywords


EID: 78349295979     PISSN: 16154150     EISSN: 16154169     Source Type: Journal    
DOI: 10.1002/adsc.201000394     Document Type: Article
Times cited : (28)

References (53)
  • 35
    • 68149142643 scopus 로고    scopus 로고
    • 2-catalyzed cyclization of 1-(indol-2-yl)-2,3-allenols provides an efficient entry to various unsymmetrical 1,4-dialkylcarbazoles, see:
    • 2-catalyzed cyclization of 1-(indol-2-yl)-2,3-allenols provides an efficient entry to various unsymmetrical 1,4-dialkylcarbazoles, see:, W. Kong, C. Fu, S. Ma, Chem. Commun. 2009, 4572 - 4574.
    • (2009) Chem. Commun. , pp. 4572-4574
    • Kong, W.1    Fu, C.2    Ma, S.3
  • 40
    • 78349271835 scopus 로고    scopus 로고
    • Perspective
    • Perspective
  • 50
    • 0007173238 scopus 로고
    • Elimination of nitrous acid from β-nitro ketones provides the corresponding α,β-unsaturated ketones which are actually identified in the reaction mixture, see.
    • Elimination of nitrous acid from β-nitro ketones provides the corresponding α,β-unsaturated ketones which are actually identified in the reaction mixture, see:, R. Fusco, S. Rossi, Chem. Ind. (London, U.K.) 1957, 1650.
    • (1957) Chem. Ind. (London, U.K.) , pp. 1650
    • Fusco, R.1    Rossi, S.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.