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Volumn 72, Issue 7, 2007, Pages 2543-2546

Nitrile-promoted Rh-catalyzed intermolecular hydroacylation of olefins with salicylaldehyde

Author keywords

[No Author keywords available]

Indexed keywords

ACYLATION; ALDEHYDES; CATALYSIS; CYANIDES; REGIOSELECTIVITY; RHODIUM;

EID: 34047192363     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo062501u     Document Type: Article
Times cited : (41)

References (26)
  • 3
    • 0037013636 scopus 로고    scopus 로고
    • and references cited therein
    • (c) Jun, C.-H.; Moon, C. W.; Lee, D.-Y. Chem.-Eur. J. 2002, 8, 2422-2428 and references cited therein.
    • (2002) Chem.-Eur. J , vol.8 , pp. 2422-2428
    • Jun, C.-H.1    Moon, C.W.2    Lee, D.-Y.3
  • 12
    • 33845204295 scopus 로고    scopus 로고
    • Recently, Willis and coworkers reported Rh-catalyzed intermolecular hydroacylation of monoolefins with β-sulfido aldehyde by using cationic Rh-complex having a P-O-P diphosphine ligand. See
    • Recently, Willis and coworkers reported Rh-catalyzed intermolecular hydroacylation of monoolefins with β-sulfido aldehyde by using cationic Rh-complex having a P-O-P diphosphine ligand. See: Moxham, G. L.; Randell-Sly, H. E.; Brayshaw, S. K.; Woodward, R. L.; Weller, A. S.; Willis, M. C. Angew. Chem., Int. Ed. 2006, 45, 7618-7622.
    • (2006) Angew. Chem., Int. Ed , vol.45 , pp. 7618-7622
    • Moxham, G.L.1    Randell-Sly, H.E.2    Brayshaw, S.K.3    Woodward, R.L.4    Weller, A.S.5    Willis, M.C.6
  • 13
    • 0242438878 scopus 로고    scopus 로고
    • Rh-catalyzed hydroformylation of alkenylnitriles. See
    • Rh-catalyzed hydroformylation of alkenylnitriles. See: Lambers-Verstappen, M. M. H.; de Vries, J. G. Adv. Synth. Catal. 2003, 345, 478-482.
    • (2003) Adv. Synth. Catal , vol.345 , pp. 478-482
    • Lambers-Verstappen, M.M.H.1    de Vries, J.G.2
  • 14
    • 34047228441 scopus 로고    scopus 로고
    • Ru- and Co-catalyzed intermolecular hydroacylations. (a) Lenges, C. P.; White, P. S.; Brookhart, M. J. Am. Chem. Soc. 1998, 120, 6955-6979.
    • Ru- and Co-catalyzed intermolecular hydroacylations. (a) Lenges, C. P.; White, P. S.; Brookhart, M. J. Am. Chem. Soc. 1998, 120, 6955-6979.
  • 20
    • 34047217157 scopus 로고    scopus 로고
    • Addition of NaOAc may deprotonate the phenolic hydroxyl group and accelerate the reaction
    • Addition of NaOAc may deprotonate the phenolic hydroxyl group and accelerate the reaction.
  • 25
    • 34047230003 scopus 로고    scopus 로고
    • Willis and coworkers reported that the Rh-catalyzed hydroacylation of 4-cyanostyrene with β-sulfido aldehyde was superior to that of styrene (ref 4). There may be two possibilities: one reason is the reactivity of 4-cyanostyrene by an electron-withdrawing group as reported, and the other reason may be coordination of the CN group to the Rh-metal to change the activity of the Rh-complex.
    • Willis and coworkers reported that the Rh-catalyzed hydroacylation of 4-cyanostyrene with β-sulfido aldehyde was superior to that of styrene (ref 4). There may be two possibilities: one reason is the reactivity of 4-cyanostyrene by an electron-withdrawing group as reported, and the other reason may be coordination of the CN group to the Rh-metal to change the activity of the Rh-complex.
  • 26
    • 33750488411 scopus 로고    scopus 로고
    • Rh-catalyzed branch-selective hydroacylation of styrene. See:, Int. Ed, and references therein
    • Rh-catalyzed branch-selective hydroacylation of styrene. See: Hong, Y.-T.; Barchuk, A.; Krische, M. J. Angew. Chem., Int. Ed. 2006, 45, 6885-6888 and references therein.
    • (2006) Angew. Chem , vol.45 , pp. 6885-6888
    • Hong, Y.-T.1    Barchuk, A.2    Krische, M.J.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.