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Volumn 73, Issue 1, 2008, Pages 298-300

Rhodium-catalyzed oxidative coupling of triarylmethanols with internal alkynes via successive C-H and C-C bond cleavages

Author keywords

[No Author keywords available]

Indexed keywords

BOND CLEAVAGES; OXIDATIVE COUPLINGS;

EID: 37549027556     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo7022087     Document Type: Article
Times cited : (121)

References (61)
  • 39
    • 37549071228 scopus 로고    scopus 로고
    • Catalytic reactions involving β-carbon elimination in Rh(I) alcoholates: (a) Reference 5c.
    • Catalytic reactions involving β-carbon elimination in Rh(I) alcoholates: (a) Reference 5c.
  • 40
    • 37549050315 scopus 로고    scopus 로고
    • Reference 5f
    • (b) Reference 5f.
  • 43
    • 34247896944 scopus 로고    scopus 로고
    • For examples of retro-allylation of homoallyl alcohols, see: (e) Jang, M, Hayashi, S, Hirano, K, Yorimitsu, H, Oshima, K. Tetrahedron Lett. 2007, 48, 4003
    • For examples of retro-allylation of homoallyl alcohols, see: (e) Jang, M.; Hayashi, S.; Hirano, K.; Yorimitsu, H.; Oshima, K. Tetrahedron Lett. 2007, 48, 4003.
  • 45
    • 33947293932 scopus 로고    scopus 로고
    • 2: (a) Whitesides, G. M.; Ehmann, W. J. J. Am. Chem. Soc. 1970, 92, 5625.
    • 2: (a) Whitesides, G. M.; Ehmann, W. J. J. Am. Chem. Soc. 1970, 92, 5625.
  • 47
    • 37549070854 scopus 로고    scopus 로고
    • Reference 5h
    • (c) Reference 5h.
  • 50
    • 37549054844 scopus 로고    scopus 로고
    • 2H.
    • 2H.
  • 51
    • 37549059727 scopus 로고    scopus 로고
    • Reference 5a. o-Dihalobenzenes.
    • (g) Reference 5a. o-Dihalobenzenes.
  • 53
    • 37549065295 scopus 로고    scopus 로고
    • Reactions of (4-methylphenyl)- and (4-fluorophenyl)diphenylmethanols with 2a under similar conditions gave mixtures of 6-substituted and unsubstituted 1,2,3,4-tetraphenylnaphthalenes (6-Me/6-H = ca. 1:1, 6-F/6-H = ca. 1:4).
    • Reactions of (4-methylphenyl)- and (4-fluorophenyl)diphenylmethanols with 2a under similar conditions gave mixtures of 6-substituted and unsubstituted 1,2,3,4-tetraphenylnaphthalenes (6-Me/6-H = ca. 1:1, 6-F/6-H = ca. 1:4).
  • 54
    • 37549030302 scopus 로고    scopus 로고
    • Ir-Catalyzed reactions of benzoic acid with 5a and 5b gave the corresponding tetraalkylnaphthalenes in low yields (10-20%). See reference 5a.
    • Ir-Catalyzed reactions of benzoic acid with 5a and 5b gave the corresponding tetraalkylnaphthalenes in low yields (10-20%). See reference 5a.
  • 56
    • 0037051266 scopus 로고    scopus 로고
    • Rh-catalyzed oxidative coupling of unactivated aromatic compounds with alkenes has been reported: (a) Matsumoto, T.; Periana, R. A.; Taube, D. J.; Yoshida, H. J. Catal. 2002, 206, 272.
    • Rh-catalyzed oxidative coupling of unactivated aromatic compounds with alkenes has been reported: (a) Matsumoto, T.; Periana, R. A.; Taube, D. J.; Yoshida, H. J. Catal. 2002, 206, 272.
  • 58
    • 37049076533 scopus 로고    scopus 로고
    • For examples of rhodium-catalyzed aerobic oxidation, see: (a) Fazlur-Rahman, A. K, Tsai, J.-C, Nicholas, K. M. J. Chem. Soc, Chem. Commun. 1992, 1334
    • For examples of rhodium-catalyzed aerobic oxidation, see: (a) Fazlur-Rahman, A. K.; Tsai, J.-C.; Nicholas, K. M. J. Chem. Soc., Chem. Commun. 1992, 1334.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.