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Volumn 10, Issue 13, 2008, Pages 2721-2724

Synthesis of indolines via a domino Cu-catalyzed amidation/cyclization reaction

Author keywords

[No Author keywords available]

Indexed keywords

COPPER; INDOLE DERIVATIVE; INDOLINE;

EID: 51649124289     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol8008792     Document Type: Article
Times cited : (105)

References (45)
  • 1
    • 0034728665 scopus 로고    scopus 로고
    • For recent examples of indoline syntheses based on non-metal-catalyzed or radical processes, see: a
    • For recent examples of indoline syntheses based on non-metal-catalyzed or radical processes, see: (a) Nicolaou, K. C.; Roecker, A. J.; Pfefferkorn, J. A.; Cao, G.-Q. J. Am. Chem. Soc. 2000, 122, 2966.
    • (2000) J. Am. Chem. Soc , vol.122 , pp. 2966
    • Nicolaou, K.C.1    Roecker, A.J.2    Pfefferkorn, J.A.3    Cao, G.-Q.4
  • 22
    • 48849113342 scopus 로고    scopus 로고
    • For a Pd-catalyzed C-H activation approach, see: d
    • For a Pd-catalyzed C-H activation approach, see: (d) Watanabe, T.; Oishi, S.; Fujii, N.; Ohno, H. Org. Lett. 2008, 10, 1759.
    • (2008) Org. Lett , vol.10 , pp. 1759
    • Watanabe, T.1    Oishi, S.2    Fujii, N.3    Ohno, H.4
  • 33
    • 37249017443 scopus 로고    scopus 로고
    • In this case, the Pd-catalyzed amination proceeds intramolecularly: (f) Thansandote, P.; Raemy, M.; Rudolph, A.; Lautens, M. Org. Lett. 2007, 9, 5255.
    • In this case, the Pd-catalyzed amination proceeds intramolecularly: (f) Thansandote, P.; Raemy, M.; Rudolph, A.; Lautens, M. Org. Lett. 2007, 9, 5255.
  • 34
    • 0346749657 scopus 로고    scopus 로고
    • For recent reviews on Cu-catalyzed C-N bond forming reactions, see: a
    • For recent reviews on Cu-catalyzed C-N bond forming reactions, see: (a) Kunz, K.; Scholz, U.; Ganzer, D. Synlett 2003, 2428.
    • (2003) Synlett , pp. 2428
    • Kunz, K.1    Scholz, U.2    Ganzer, D.3
  • 40
    • 59949090385 scopus 로고    scopus 로고
    • For evidence of intramolecular Cu-catalyzed hydroamidation of an unsaturated moiety, see ref 11b
    • For evidence of intramolecular Cu-catalyzed hydroamidation of an unsaturated moiety, see ref 11b.
  • 41
    • 33750685325 scopus 로고    scopus 로고
    • For recent examples of the synthesis of enantiomerically enriched indolines, see
    • (a) For recent examples of the synthesis of enantiomerically enriched indolines, see: Arp, F. O.; Fu, G. C. J. Am. Chem. Soc. 2006, 128, 14265.
    • (2006) J. Am. Chem. Soc , vol.128 , pp. 14265
    • Arp, F.O.1    Fu, G.C.2
  • 44
    • 0001694704 scopus 로고    scopus 로고
    • For examples of trans-1,2,3,4,4a,9a-hexahydrocarbazoles, see: (a) Smolinsky, G. J. Am. Chem. Soc. 1961, 83, 2489
    • For examples of trans-1,2,3,4,4a,9a-hexahydrocarbazoles, see: (a) Smolinsky, G. J. Am. Chem. Soc. 1961, 83, 2489.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.