메뉴 건너뛰기




Volumn 50, Issue 31, 2009, Pages 4526-4528

Air-tolerant C-C bond formation via organometallic ruthenium catalysis: diverse catalytic pathways involving (C5Me5)Ru or (C5H5)Ru are robust to molecular oxygen

Author keywords

[No Author keywords available]

Indexed keywords

ALKYNE; CARBON; ORGANOMETALLIC COMPOUND; OXYGEN; RUTHENIUM;

EID: 66949126158     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2009.05.079     Document Type: Article
Times cited : (15)

References (68)
  • 2
    • 1442360753 scopus 로고    scopus 로고
    • Grubbs R.H. (Ed), Wiley-VCH, Weinheim
    • In: Grubbs R.H. (Ed). Handbook of Metathesis (2003), Wiley-VCH, Weinheim
    • (2003) Handbook of Metathesis
  • 3
    • 0003464697 scopus 로고    scopus 로고
    • Fürstner A. (Ed), Springer, Berlin, Heidelberg
    • In: Fürstner A. (Ed). Topics in Organometallic Chemistry Vol. 1 (1998), Springer, Berlin, Heidelberg
    • (1998) Topics in Organometallic Chemistry , vol.1
  • 6
    • 15744379429 scopus 로고    scopus 로고
    • Bruneau C., and Dixneuf P.H. (Eds), Springer, Berlin
    • In: Bruneau C., and Dixneuf P.H. (Eds). Ruthenium Catalysts and Fine Chemistry (2004), Springer, Berlin
    • (2004) Ruthenium Catalysts and Fine Chemistry
  • 7
    • 17844369291 scopus 로고    scopus 로고
    • Murahashi S.-I. (Ed), Wiley-VCH, Weinheim
    • In: Murahashi S.-I. (Ed). Ruthenium in Organic Synthesis (2004), Wiley-VCH, Weinheim
    • (2004) Ruthenium in Organic Synthesis
  • 8
    • 0035984037 scopus 로고    scopus 로고
    • Although there is no detailed review focused on air-tolerant organometallic transformations, examples can be found in:
    • Although there is no detailed review focused on air-tolerant organometallic transformations, examples can be found in:. Li C.-J. Acc. Chem. Res. 35 (2002) 533
    • (2002) Acc. Chem. Res. , vol.35 , pp. 533
    • Li, C.-J.1
  • 10
    • 36348984494 scopus 로고    scopus 로고
    • Lindström U.M. (Ed), Blackwell Publishing
    • Li C.-J. In: Lindström U.M. (Ed). Organic Reactions in Water (2007), Blackwell Publishing
    • (2007) Organic Reactions in Water
    • Li, C.-J.1
  • 21
    • 41749125072 scopus 로고    scopus 로고
    • Bruneau C., and Dixneuf P.H. (Eds), Springer, Berlin
    • Li C.-J. In: Bruneau C., and Dixneuf P.H. (Eds). Ruthenium Catalysts and Fine Chemistry. Topics in Organometallic Chemistry Vol. 11 (2004), Springer, Berlin 321
    • (2004) Topics in Organometallic Chemistry , vol.11 , pp. 321
    • Li, C.-J.1
  • 22
    • 66949116087 scopus 로고    scopus 로고
    • see also 1g
    • see also 1g.
  • 23
    • 0035915369 scopus 로고    scopus 로고
    • For a note on oxygen-tolerance of ruthenium-catalyzed alkene-alkyne coupling, see:
    • For a note on oxygen-tolerance of ruthenium-catalyzed alkene-alkyne coupling, see:. Trost B.M., Pinkerton A.B., Toste F.D., and Sperrle M. J. Am. Chem. Soc. 123 (2001) 12504
    • (2001) J. Am. Chem. Soc. , vol.123 , pp. 12504
    • Trost, B.M.1    Pinkerton, A.B.2    Toste, F.D.3    Sperrle, M.4
  • 27
    • 84989535702 scopus 로고
    • For ruthenium-catalyzed oxidative coupling of alkenes with arenes, see:
    • Foltynowicz Z., Pietraszuk C., and Marciniec B. Appl. Organomet. Chem. 7 (1993) 539 For ruthenium-catalyzed oxidative coupling of alkenes with arenes, see:
    • (1993) Appl. Organomet. Chem. , vol.7 , pp. 539
    • Foltynowicz, Z.1    Pietraszuk, C.2    Marciniec, B.3
  • 29
    • 0033814733 scopus 로고    scopus 로고
    • For ruthenium-catalyzed oxidative coupling of phenols leading to biaryls in the presence of molecular oxygen, see:
    • For ruthenium-catalyzed oxidative coupling of phenols leading to biaryls in the presence of molecular oxygen, see:. Irie R., Masutani K., and Katsuki T. Synlett (2000) 1433
    • (2000) Synlett , pp. 1433
    • Irie, R.1    Masutani, K.2    Katsuki, T.3
  • 37
    • 66949180876 scopus 로고    scopus 로고
    • note
    • See Supplementary data for experimental details.
  • 38
    • 23044452751 scopus 로고    scopus 로고
    • For reviews, see:. Murahashi S.-I. (Ed), Wiley-VCH, Weinheim
    • For reviews, see:. Yamamoto Y., and Itoh K. In: Murahashi S.-I. (Ed). Ruthenium in Organic Synthesis (2004), Wiley-VCH, Weinheim 95
    • (2004) Ruthenium in Organic Synthesis , pp. 95
    • Yamamoto, Y.1    Itoh, K.2
  • 39
    • 15044358496 scopus 로고    scopus 로고
    • Ruthenium Catalysts and Fine Chemistry
    • Bruneau C., and Dixneuf P.H. (Eds), Springer, Berlin
    • Dérien S., Monnier F., and Dixneuf P.H. Ruthenium Catalysts and Fine Chemistry. In: Bruneau C., and Dixneuf P.H. (Eds). Topics in Organometallic Chemistry Vol. 11 (2004), Springer, Berlin 1
    • (2004) Topics in Organometallic Chemistry , vol.11 , pp. 1
    • Dérien, S.1    Monnier, F.2    Dixneuf, P.H.3
  • 49
    • 0001800335 scopus 로고
    • For leading references on metal-catalyzed [2+2+2] cycloadditions, see:
    • For leading references on metal-catalyzed [2+2+2] cycloadditions, see:. Vollhardt K.P.C. Acc. Chem. Res. 10 (1977) 1
    • (1977) Acc. Chem. Res. , vol.10 , pp. 1
    • Vollhardt, K.P.C.1
  • 50
    • 0000814758 scopus 로고
    • Trost B.M., and Fleming I. (Eds), Pergamon Press, Oxford
    • Schore N.E. In: Trost B.M., and Fleming I. (Eds). Comprehensive Organic Synthesis Vol. 5 (1992), Pergamon Press, Oxford 1129
    • (1992) Comprehensive Organic Synthesis , vol.5 , pp. 1129
    • Schore, N.E.1
  • 54
    • 66949148414 scopus 로고    scopus 로고
    • note
    • We note that processes 16+14→17 and 16+21→23 in DCE are not stopped in the presence of strongly acidic or basic environments (i.e., 34 mM TFA, and 17 mM DBU, respectively).
  • 55
    • 17844369291 scopus 로고    scopus 로고
    • For C-C bond formation via π-allylruthenium intermediates, see:. Murahashi S.-I. (Ed), Wiley-VCH, Weinheim
    • For C-C bond formation via π-allylruthenium intermediates, see:. Kondo T., and Mitsudo T. In: Murahashi S.-I. (Ed). Ruthenium in Organic Synthesis (2004), Wiley-VCH, Weinheim 129
    • (2004) Ruthenium in Organic Synthesis , pp. 129
    • Kondo, T.1    Mitsudo, T.2
  • 57
    • 0000213281 scopus 로고
    • For seminal work on ruthenium-catalyzed allylations, see:
    • For seminal work on ruthenium-catalyzed allylations, see:. Minami I., Shimizu I., and Tsuji J. J. Organomet. Chem. 296 (1985) 269
    • (1985) J. Organomet. Chem. , vol.296 , pp. 269
    • Minami, I.1    Shimizu, I.2    Tsuji, J.3
  • 67
    • 66949127635 scopus 로고    scopus 로고
    • of note is the discussion of air stability relating to isolated ruthenium complexes in 16a.
    • of note is the discussion of air stability relating to isolated ruthenium complexes in 16a.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.