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Volumn 51, Issue 48, 2012, Pages 12115-12119

Functionalization of Csp3-H and Csp 2-H bonds: Synthesis of spiroindenes by enolate-directed ruthenium-catalyzed oxidative annulation of alkynes with 2-aryl-1,3-dicarbonyl compounds

Author keywords

annulation; C H functionalization; oxidation; ruthenium; synthetic methods

Indexed keywords

1 ,3-DICARBONYL; ANNULATION; C-H FUNCTIONALIZATION; CARBOCYCLES; DIVERSE RANGE; FUNCTIONALIZATIONS; H-BONDS; OXIDATIVE ANNULATION; QUATERNARY CENTERS; SYNTHETIC METHODS;

EID: 84870021516     PISSN: 14337851     EISSN: 15213773     Source Type: Journal    
DOI: 10.1002/anie.201207170     Document Type: Article
Times cited : (119)

References (79)
  • 1
  • 2
    • 77957204974 scopus 로고    scopus 로고
    • For a Review of rhodium-catalyzed oxidative annulations of alkynes, see.
    • For a Review of rhodium-catalyzed oxidative annulations of alkynes, see:, T. Satoh, M. Miura, Chem. Eur. J. 2010, 16, 11212-11222.
    • (2010) Chem. Eur. J. , vol.16 , pp. 11212-11222
    • Satoh, T.1    Miura, M.2
  • 10
    • 79551654576 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2011, 50, 1338-1341
    • (2011) Angew. Chem. Int. Ed. , vol.50 , pp. 1338-1341
  • 13
    • 84865841810 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2012, 51, 9372-9376
    • (2012) Angew. Chem. Int. Ed. , vol.51 , pp. 9372-9376
  • 16
    • 79959862124 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2011, 50, 6379-6382
    • (2011) Angew. Chem. Int. Ed. , vol.50 , pp. 6379-6382
  • 31
    • 70349976206 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2009, 48, 8078-8081
    • (2009) Angew. Chem. Int. Ed. , vol.48 , pp. 8078-8081
  • 44
    • 72449170089 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2009, 48, 9792-9826.
    • (2009) Angew. Chem. Int. Ed. , vol.48 , pp. 9792-9826
  • 47
    • 70349653362 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2009, 48, 7895-7898
    • (2009) Angew. Chem. Int. Ed. , vol.48 , pp. 7895-7898
  • 51
    • 47049108951 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2008, 47, 4019-4022
    • (2008) Angew. Chem. Int. Ed. , vol.47 , pp. 4019-4022
  • 60
    • 79955379597 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2011, 50, 4169-4172
    • (2011) Angew. Chem. Int. Ed. , vol.50 , pp. 4169-4172
  • 62
    • 81255209300 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2011, 50, 11098-11102
    • (2011) Angew. Chem. Int. Ed. , vol.50 , pp. 11098-11102
  • 64
    • 84859746984 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2012, 51, 3948-3952.
    • (2012) Angew. Chem. Int. Ed. , vol.51 , pp. 3948-3952
  • 65
    • 77954637248 scopus 로고    scopus 로고
    • For the synthesis of pyrroles by oxidative annulation of enamines with alkynes, involving C sp 3 -H functionalization, see.
    • For the synthesis of pyrroles by oxidative annulation of enamines with alkynes, involving C sp 3 -H functionalization, see:, S. Rakshit, F. W. Patureau, F. Glorius, J. Am. Chem. Soc. 2010, 132, 9585-9587.
    • (2010) J. Am. Chem. Soc. , vol.132 , pp. 9585-9587
    • Rakshit, S.1    Patureau, F.W.2    Glorius, F.3
  • 78
    • 84871043994 scopus 로고    scopus 로고
    • The structures of the spiroindenes 3 i and 3 j were confirmed by X-ray crystallography. See the Supporting Information for details. CCDC 894550 (3 i) and CCDC 897478 (3 j) contain the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via
    • The structures of the spiroindenes 3 i and 3 j were confirmed by X-ray crystallography. See the Supporting Information for details. CCDC 894550 (3 i) and CCDC 897478 (3 j) 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.
  • 79
    • 77953892735 scopus 로고    scopus 로고
    • An intermediate similar to ruthenacycle 8 has been proposed previously in the palladium-catalyzed synthesis of phenanthrone derivatives by dual C-H activation.
    • An intermediate similar to ruthenacycle 8 has been proposed previously in the palladium-catalyzed synthesis of phenanthrone derivatives by dual C-H activation:, P. Gandeepan, K. Parthasarathy, C.-H. Cheng, J. Am. Chem. Soc. 2010, 132, 8569-8571.
    • (2010) J. Am. Chem. Soc. , vol.132 , pp. 8569-8571
    • Gandeepan, P.1    Parthasarathy, K.2    Cheng, C.-H.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.