메뉴 건너뛰기




Volumn 26, Issue 23, 2007, Pages 5680-5686

Coupling Pd-catalyzed alcohol oxidation to olefin functionalization: Hydrohalogenation/hydroalkoxylation of styrenes

Author keywords

[No Author keywords available]

Indexed keywords

ALCOHOL OXIDATION; HYDROALKOXYLATION; HYDROHALOGENATION; MECHANISTIC EXPERIMENTS; OLEFIN FUNCTIONALIZATION;

EID: 36248959890     PISSN: 02767333     EISSN: None     Source Type: Journal    
DOI: 10.1021/om700675z     Document Type: Article
Times cited : (35)

References (53)
  • 16
    • 3543083464 scopus 로고    scopus 로고
    • For examples of hydroalkoxylation reactions not requiring a triflate counterion, see: (a) Qian, H, Han, X, Widenhoefer, R. A. J. Am. Chem. Soc. 2004, 126, 9536
    • For examples of hydroalkoxylation reactions not requiring a triflate counterion, see: (a) Qian, H.; Han, X.; Widenhoefer, R. A. J. Am. Chem. Soc. 2004, 126, 9536.
  • 28
    • 17744365015 scopus 로고    scopus 로고
    • For aerobic Pd-catalyzed oxidations of longer chain alcohols, see
    • (b) For aerobic Pd-catalyzed oxidations of longer chain alcohols, see: Schultz, M. J.; Hamilton, S. S.; Jensen, D. R.; Sigman, M. S. J. Org. Chem. 2005, 70, 3343.
    • (2005) J. Org. Chem , vol.70 , pp. 3343
    • Schultz, M.J.1    Hamilton, S.S.2    Jensen, D.R.3    Sigman, M.S.4
  • 32
    • 84858475284 scopus 로고    scopus 로고
    • 2 (see Supporting Information).
    • 2 (see Supporting Information).
  • 35
    • 36249028959 scopus 로고    scopus 로고
    • See Supporting Information
    • See Supporting Information.
  • 39
    • 84858465942 scopus 로고    scopus 로고
    • It is also possible that the ratio of K and L is affected by the electronics of the aryl ring via different stabilization of the π-benzyl complex see ref 21
    • It is also possible that the ratio of K and L is affected by the electronics of the aryl ring via different stabilization of the π-benzyl complex (see ref 21).
  • 45
    • 0000916635 scopus 로고    scopus 로고
    • For a proposed mechanism of a Pd-catalyzed H/D exchange via the enol form of acetone, see: Portnoy, M.; Milstein, D. Organometallics 1994, 13, 600.
    • For a proposed mechanism of a Pd-catalyzed H/D exchange via the enol form of acetone, see: Portnoy, M.; Milstein, D. Organometallics 1994, 13, 600.
  • 46
    • 36249015677 scopus 로고    scopus 로고
    • D incorporation into styrene could not be quantified due to the loss of H (D) in the mass spectrometer. Additionally, different product ratios were observed for reactions involving deuterated alcohol and/or styrene, and deuterium incorporation was observed in the Wacker product, which should originate from deuterated styrene
    • D incorporation into styrene could not be quantified due to the loss of H (D) in the mass spectrometer. Additionally, different product ratios were observed for reactions involving deuterated alcohol and/or styrene, and deuterium incorporation was observed in the Wacker product, which should originate from deuterated styrene.
  • 49
    • 84858477792 scopus 로고    scopus 로고
    • 29
    • 29


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.