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Volumn 129, Issue 43, 2007, Pages 13321-13326

Palladium-catalyzed cross-coupling reactions in one-pot multicatalytic processes

Author keywords

[No Author keywords available]

Indexed keywords

AMINO ACIDS; CARBONYLATION; CATALYST ACTIVITY; COPPER; HYDROXYLATION; OLEFINS; PARAFFINS; SYNTHESIS (CHEMICAL);

EID: 35848951618     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja0733235     Document Type: Article
Times cited : (83)

References (123)
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    • Selected examples: (a) Murelli, R. P.; Snapper, M. L. Org. Lett. 2007, 9, 1749-1752.
    • Selected examples: (a) Murelli, R. P.; Snapper, M. L. Org. Lett. 2007, 9, 1749-1752.
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    • These terms have been essentially defined to address mechanistic implications of these various one-pot processeses; for additional discussions, see: Seigal, B. A, Fajardo, C, Snapper, M. L. J. Am. Chem. Soc. 2005, 127, 16329-16332 and references therein
    • These terms have been essentially defined to address mechanistic implications of these various one-pot processeses; for additional discussions, see: Seigal, B. A.; Fajardo, C.; Snapper, M. L. J. Am. Chem. Soc. 2005, 127, 16329-16332 and references therein.
  • 60
    • 33749009772 scopus 로고    scopus 로고
    • See for instance: a
    • See for instance: (a) Zhang, Z. H.; Liebeskind, L. S. Org. Lett. 2006, 8, 4331-4333.
    • (2006) Org. Lett , vol.8 , pp. 4331-4333
    • Zhang, Z.H.1    Liebeskind, L.S.2
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    • Ferre-Filmon, K.; Delaude, L.; Demonceau, A1; Noels, A. F. Eur. J. Org. Chem. 2005, 3319-3325.
    • (a) Ferre-Filmon, K.; Delaude, L.; Demonceau, A1; Noels, A. F. Eur. J. Org. Chem. 2005, 3319-3325.
  • 99
    • 35848970437 scopus 로고    scopus 로고
    • Surprisingly, the use of the more reactive 4-iodotoluene as a coupling agent did not produce the desired product in a better yield. Only 45% was obtained to produce 1 using CuCl and the Heck reaction conditions described in Table 1, entry 4.
    • Surprisingly, the use of the more reactive 4-iodotoluene as a coupling agent did not produce the desired product in a better yield. Only 45% was obtained to produce 1 using CuCl and the Heck reaction conditions described in Table 1, entry 4.
  • 100
    • 35848963496 scopus 로고    scopus 로고
    • The 1,1-disubstituted alkene was also isolated 5-10, in some cases and accounted for some of the lower yields
    • The 1,1-disubstituted alkene was also isolated (5-10%) in some cases and accounted for some of the lower yields.
  • 103
    • 35848964159 scopus 로고    scopus 로고
    • Aldehyde 11 is readily available in five steps from commercially available 3,4-dimethoxybenzaldehyde. See the Supporting Information for details.
    • Aldehyde 11 is readily available in five steps from commercially available 3,4-dimethoxybenzaldehyde. See the Supporting Information for details.
  • 104
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    • Ketone 13 is readily available in four steps from known 4-(hydroxymethyl)-2-methoxyphenyl acetate. See the Supporting Information for details.
    • Ketone 13 is readily available in four steps from known 4-(hydroxymethyl)-2-methoxyphenyl acetate. See the Supporting Information for details.
  • 123
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    • IMesCuCl: Chemical Equation Presented
    • IMesCuCl: (Chemical Equation Presented)


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.