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Volumn 77, Issue 9, 2012, Pages 4414-4419

Lewis acid-catalyzed, copper(II)-mediated synthesis of heteroaryl thioethers under base-free conditions

Author keywords

[No Author keywords available]

Indexed keywords

HETEROARENES; LEWIS ACID; THIOETHERS; THIOLATION;

EID: 84860605905     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo202624s     Document Type: Article
Times cited : (179)

References (46)
  • 16
    • 79951816256 scopus 로고    scopus 로고
    • For an example of Cu-mediated azole C-H dehydrogenative cross-coupling, in which C-H bond cleavage was not involved in the rate-determining step, see
    • For an example of Cu-mediated azole C-H dehydrogenative cross-coupling, in which C-H bond cleavage was not involved in the rate-determining step, see: Kitahara, M.; Umeda, N.; Hirano, K.; Satoh, T.; Miura, M. J. Am. Chem. Soc. 2010, 133, 2160
    • (2010) J. Am. Chem. Soc. , vol.133 , pp. 2160
    • Kitahara, M.1    Umeda, N.2    Hirano, K.3    Satoh, T.4    Miura, M.5
  • 21
    • 0010597557 scopus 로고    scopus 로고
    • I-promoted carboxylated-assisted concerted metalation-deprotonation of azole
    • I-promoted carboxylated-assisted concerted metalation-deprotonation of azole: Kondo, Y.; Komine, T.; Sakamoto, T. Org. Lett. 2000, 2, 3111
    • (2000) Org. Lett. , vol.2 , pp. 3111
    • Kondo, Y.1    Komine, T.2    Sakamoto, T.3
  • 23
    • 81755163019 scopus 로고    scopus 로고
    • For Lewis acid catalyzed C-H/N-H amination of azoles and thiazoles via an electrophilic addition/oxidative rearomatization sequence, see
    • For Lewis acid catalyzed C-H/N-H amination of azoles and thiazoles via an electrophilic addition/oxidative rearomatization sequence, see: Wertz, S.; Kodama, S.; Studer, A. Angew. Chem., Int. Ed. 2011, 50, 11511
    • (2011) Angew. Chem., Int. Ed. , vol.50 , pp. 11511
    • Wertz, S.1    Kodama, S.2    Studer, A.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.