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Volumn 17, Issue 18, 2015, Pages 4612-4615

Design of an Indolylphosphine Ligand for Reductive Elimination-Demanding Monoarylation of Acetone Using Aryl Chlorides

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EID: 84941896212     PISSN: 15237060     EISSN: 15237052     Source Type: Journal    
DOI: 10.1021/acs.orglett.5b02344     Document Type: Article
Times cited : (61)

References (51)
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    • Apart from aryl halides, aryl imidazolylsuflonates were found to be applicable substrates; see: Ackermann, L.; Mehta, V. P. Chem.-Eur. J. 2012, 18, 10230 10.1002/chem.201201394
    • (2012) Chem. - Eur. J. , vol.18 , pp. 10230
    • Ackermann, L.1    Mehta, V.P.2
  • 26
    • 84941884445 scopus 로고    scopus 로고
    • CyPF-tBu = (R)-1-[(SP)-2-(dicyclohexylphosphino)ferrocenyl]ethyldi-tert-butylphosphine. During the completion of our experimental works, a related paper appeared; see: MacQueen, P. M.; Chisholm, A. J.; Hargreaves, B. K. V.; Stradiotto, M. Chem.-Eur. J. 2015, 21, 11006 10.1002/chem.201500834
    • (2015) Chem. - Eur. J. , vol.21 , pp. 11006
    • MacQueen, P.M.1    Chisholm, A.J.2    Hargreaves, B.K.V.3    Stradiotto, M.4
  • 46
    • 51149214207 scopus 로고
    • The indicated C-3 position of indole is estimated to be 1013 times more reactive than benzene for electrophilic attack; see: Laws, A. P.; Taylor, R. J. Chem. Soc., Perkin Trans. 2 1987, 591 10.1039/p29870000591
    • (1987) J. Chem. Soc., Perkin Trans. 2 , pp. 591
    • Laws, A.P.1    Taylor, R.2
  • 49
    • 84924414753 scopus 로고    scopus 로고
    • For a recent reference describing the specially designed biaryl-type phosphine ligand for a difficult RE process, see: Li, C.; Chen, T.; Li, B.; Xiao, G.; Tang, W. Angew. Chem., Int. Ed. 2015, 54, 3792 10.1002/anie.201411518
    • (2015) Angew. Chem., Int. Ed. , vol.54 , pp. 3792
    • Li, C.1    Chen, T.2    Li, B.3    Xiao, G.4    Tang, W.5
  • 51
    • 12344337315 scopus 로고    scopus 로고
    • Ligand cost and catalyst loading become two of the most important factors in production-scale catalysis; see: Schlummer, B.; Scholz, U. Adv. Synth. Catal. 2004, 346, 1599 10.1002/adsc.200404216
    • (2004) Adv. Synth. Catal. , vol.346 , pp. 1599
    • Schlummer, B.1    Scholz, U.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.