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Volumn 72, Issue 10, 2007, Pages 3875-3879

Enantio- and regioselective heck-type reaction of arylboronic acids with 2,3-dihydrofuran

Author keywords

[No Author keywords available]

Indexed keywords

CATALYST ACTIVITY; ENANTIOSELECTIVITY; FURAN RESINS; PALLADIUM; REACTION KINETICS; REGIOSELECTIVITY;

EID: 34248525511     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo070170v     Document Type: Article
Times cited : (41)

References (61)
  • 2
    • 27544497732 scopus 로고    scopus 로고
    • Tsuji, J. Ed, Springer: Heidelberg, Germany
    • (b) Palladium in Organic Synthesis; Tsuji, J. Ed., Springer: Heidelberg, Germany, 2005; Vol. 14.
    • (2005) Palladium in Organic Synthesis , vol.14
  • 29
    • 0037116510 scopus 로고    scopus 로고
    • Only several asymmetric Heck-type transformations that are catalyzed by transition metal complexes bearing monodentate ligands are known. See for example Imbos, R, Minnaard, A. J, Feringa B. L. J. Am. Chem. Soc. 2002, 124, 184
    • (c) Only several asymmetric Heck-type transformations that are catalyzed by transition metal complexes bearing monodentate ligands are known. See for example Imbos, R.; Minnaard, A. J.; Feringa B. L. J. Am. Chem. Soc. 2002, 124, 184.
  • 46
    • 0035820028 scopus 로고    scopus 로고
    • Although kinetics might change depending on the catalyst/reactants combination See for example Rosner, T, Le Bars, J, Pfaltz, A, Blackmond, D. G. J. Am. Chem. Soc. 2001, 123, 1848, oxidative addition is very often a rate-limiting step for catalysts bearing bidentate ligands
    • Although kinetics might change depending on the catalyst/reactants combination (See for example Rosner, T.; Le Bars, J.; Pfaltz, A.; Blackmond, D. G. J. Am. Chem. Soc. 2001, 123, 1848.), oxidative addition is very often a rate-limiting step for catalysts bearing bidentate ligands.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.