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Volumn 62, Issue 49, 2006, Pages 11371-11380

Brønsted acid-promoted cyclizations of siloxy alkynes with unactivated arenes, alkenes, and alkynes

Author keywords

[No Author keywords available]

Indexed keywords

ACID; ALKENE; ALKYNE DERIVATIVE; ANION; BRONSTED ACID; CARBON; ORGANIC SOLVENT; POLYCYCLIC AROMATIC HYDROCARBON DERIVATIVE; SULFUR DERIVATIVE; TRIFLUOROMETHANE SULFONIMIDE; UNCLASSIFIED DRUG;

EID: 33750472343     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2006.06.037     Document Type: Article
Times cited : (19)

References (57)
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    • Fleming, I.1    Barbero, A.2    Walter, D.3
  • 8
    • 0242656295 scopus 로고    scopus 로고
    • For a review of ynolate anions and siloxy alkynes, see:
    • For a review of ynolate anions and siloxy alkynes, see:. Shindo M. Synthesis (2003) 2275
    • (2003) Synthesis , pp. 2275
    • Shindo, M.1
  • 9
    • 0005941701 scopus 로고
    • For a review of preparation and reactivity of alkoxy alkynes, see:. Raphael R.A., and Taylor E.C. (Eds), Interscience, New York, NY
    • For a review of preparation and reactivity of alkoxy alkynes, see:. Arens J.F. In: Raphael R.A., and Taylor E.C. (Eds). Advances in Organic Chemistry Methods and Results Vol. 2 (1960), Interscience, New York, NY 117-212
    • (1960) Advances in Organic Chemistry Methods and Results , vol.-2 , pp. 117-212
    • Arens, J.F.1
  • 17
    • 0003828015 scopus 로고
    • Wiley, New York, NY
    • Tidwell T.T. Ketenes (1995), Wiley, New York, NY
    • (1995) Ketenes
    • Tidwell, T.T.1
  • 34
    • 0000471716 scopus 로고
    • For preparation of anhydrous tert-butyl hydroperoxide, see:
    • For preparation of anhydrous tert-butyl hydroperoxide, see:. Hill J.G., Rossiter B.E., and Sharpless K.B. J. Org. Chem. 48 (1983) 3607
    • (1983) J. Org. Chem. , vol.48 , pp. 3607
    • Hill, J.G.1    Rossiter, B.E.2    Sharpless, K.B.3
  • 43
    • 33750491018 scopus 로고    scopus 로고
    • 2-promoted reactions, see:
  • 52
    • 0000960525 scopus 로고
    • For other examples of halide abstraction from hydrocarbons by carbocations, see:
    • Balog A., Geib S.J., and Curran D.P. J. Org. Chem. 60 (1995) 345 For other examples of halide abstraction from hydrocarbons by carbocations, see:
    • (1995) J. Org. Chem. , vol.60 , pp. 345
    • Balog, A.1    Geib, S.J.2    Curran, D.P.3
  • 54
    • 33750465760 scopus 로고    scopus 로고
    • 2O or AcOH is reversed (Ref. 14b). The acidity of the two acids in ionic liquid is comparable (Ref. 14c).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.