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Volumn 14, Issue 20, 2012, Pages 5370-5373

Trichlorophenyl formate: Highly reactive and easily accessible crystalline CO surrogate for palladium-catalyzed carbonylation of aryl/alkenyl halides and triflates

Author keywords

[No Author keywords available]

Indexed keywords

CARBON MONOXIDE; CHLOROCARBONIC ACID; FORMIC ACID DERIVATIVE; PALLADIUM;

EID: 84867726565     PISSN: 15237060     EISSN: 15237052     Source Type: Journal    
DOI: 10.1021/ol302593z     Document Type: Article
Times cited : (119)

References (21)
  • 16
    • 84864075375 scopus 로고    scopus 로고
    • Tsuji et al. also reported the Pd-catalyzed esterification of aryl halides using aryl formates
    • Tsuji et al. also reported the Pd-catalyzed esterification of aryl halides using aryl formates. See: Fujihara, T.; Hosoki, T.; Katafuchi, Y.; Iwai, T.; Terao, J.; Tsuji, Y. Chem. Commun. 2012, 48, 8012
    • (2012) Chem. Commun. , vol.48 , pp. 8012
    • Fujihara, T.1    Hosoki, T.2    Katafuchi, Y.3    Iwai, T.4    Terao, J.5    Tsuji, Y.6
  • 17
    • 79951846789 scopus 로고    scopus 로고
    • Tsuji et al. reported that electron-withdrawing substituents accelerated the Pd-catalyzed decarbonylation of phenyl formates
    • Tsuji et al. reported that electron-withdrawing substituents accelerated the Pd-catalyzed decarbonylation of phenyl formates; see: Katafuchi, Y.; Fujihara, T.; Iwai, T.; Terao, J.; Tsuji, Y. Adv. Synth. Catal. 2011, 353, 475
    • (2011) Adv. Synth. Catal. , vol.353 , pp. 475
    • Katafuchi, Y.1    Fujihara, T.2    Iwai, T.3    Terao, J.4    Tsuji, Y.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.