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Volumn 132, Issue 28, 2010, Pages 9602-9603

Iridium-catalyzed annulation of N -arylcarbamoyl chlorides with internal alkynes

Author keywords

[No Author keywords available]

Indexed keywords

CATALYTIC REACTIONS; INTERNAL ALKYNES; IRIDIUM COMPLEX; QUINOLONES;

EID: 77954653617     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja104153k     Document Type: Article
Times cited : (83)

References (35)
  • 10
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    • For recent reviews of carbonylative annulations using CO as a carbonyl source, see
    • For recent reviews of carbonylative annulations using CO as a carbonyl source, see: Chatani, N. Chem. Rec. 2008, 8, 201
    • (2008) Chem. Rec. , vol.8 , pp. 201
    • Chatani, N.1
  • 16
    • 60849102199 scopus 로고    scopus 로고
    • references cited therein
    • Yasui, Y. and Takemoto, Y. Chem. Rec. 2008, 8, 386 and references cited therein
    • (2008) Chem. Rec. , vol.8 , pp. 386
    • Yasui, Y.1    Takemoto, Y.2
  • 17
    • 77953321223 scopus 로고    scopus 로고
    • The 2-quinolone core is a ubiquitous subunit in many alkaloids with various biological activities, and 2-quinolones serve as valuable intermediates in organic synthesis. For examples, see
    • The 2-quinolone core is a ubiquitous subunit in many alkaloids with various biological activities, and 2-quinolones serve as valuable intermediates in organic synthesis. For examples, see: Jayashree, B. S., Thomas, S., and Nayak, Y. Med. Chem. Res. 2010, 19, 193
    • (2010) Med. Chem. Res. , vol.19 , pp. 193
    • Jayashree, B.S.1    Thomas, S.2    Nayak, Y.3
  • 19
    • 74049129435 scopus 로고    scopus 로고
    • Recently, the synthesis of 2-quinolones by intramolecular cyclization of carbamoyl chlorides bearing an alkene has been reported. See
    • Recently, the synthesis of 2-quinolones by intramolecular cyclization of carbamoyl chlorides bearing an alkene has been reported. See: Yasui, Y., Kakinokihara, I., Takeda, H., and Takemoto, Y. Synthesis 2009, 3989
    • (2009) Synthesis , pp. 3989
    • Yasui, Y.1    Kakinokihara, I.2    Takeda, H.3    Takemoto, Y.4
  • 20
    • 69549117002 scopus 로고    scopus 로고
    • For selected syntheses and functionalizations of 2-quinolones, see
    • For selected syntheses and functionalizations of 2-quinolones, see: Tang, D.-J., Tang, B.-X., and Li, J.-H. J. Org. Chem. 2009, 74, 6749
    • (2009) J. Org. Chem. , vol.74 , pp. 6749
    • Tang, D.-J.1    Tang, B.-X.2    Li, J.-H.3
  • 29
    • 0000386089 scopus 로고    scopus 로고
    • Rh-catalyzed annulation of acid chlorides with internal alkynes to give indenones via migration/reinsertion of CO has been reported. See
    • Rh-catalyzed annulation of acid chlorides with internal alkynes to give indenones via migration/reinsertion of CO has been reported. See: Kokubo, K., Matsumasa, K., Miura, M., and Nomura, M. J. Org. Chem. 1996, 61, 6941
    • (1996) J. Org. Chem. , vol.61 , pp. 6941
    • Kokubo, K.1    Matsumasa, K.2    Miura, M.3    Nomura, M.4
  • 32
    • 77954632529 scopus 로고    scopus 로고
    • See the Supporting Information for details.
    • See the Supporting Information for details.
  • 34
    • 11144334580 scopus 로고    scopus 로고
    • For oxidative addition of carbamoyl chlorides to palladium, see:, and references cited therein
    • For oxidative addition of carbamoyl chlorides to palladium, see: Hiwatari, K., Kayaki, Y., Okita, K., Ukai, T., Shimizu, I., and Yamamoto, A. Bull. Chem. Soc. Jpn. 2004, 77, 2237 and references cited therein
    • (2004) Bull. Chem. Soc. Jpn. , vol.77 , pp. 2237
    • Hiwatari, K.1    Kayaki, Y.2    Okita, K.3    Ukai, T.4    Shimizu, I.5    Yamamoto, A.6
  • 35
    • 0001080640 scopus 로고
    • For the synthesis and characterization of arylamide-iridacycle complexes from amines and CO, see
    • For the synthesis and characterization of arylamide-iridacycle complexes from amines and CO, see: Rahim, M., Bushweller, H., and Ahmed, K. J. Organometallics 1994, 13, 4952
    • (1994) Organometallics , vol.13 , pp. 4952
    • Rahim, M.1    Bushweller, H.2    Ahmed, K.J.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.