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Volumn 349, Issue 10, 2007, Pages 1725-1737

Metal triflate-catalyzed regio- And stereoselective friedelCrafts alkenylation of arenes with alkynes in an ionic liquid: Scope and mechanism

Author keywords

Enhanced Lewis acidity; Friedel crafts alkenylation; Hydroarylation; Ionic liquids containing non coordinating anions; Vinyl cation intermediates

Indexed keywords


EID: 34547216324     PISSN: 16154150     EISSN: 15213897     Source Type: Journal    
DOI: 10.1002/adsc.200700039     Document Type: Article
Times cited : (111)

References (60)
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    • However, it has recently been suggested by Tunge et al. that the Fujiwara hydroarylation occurs rather via typical Friedel-Crafts alkenylation pathway; see
    • However, it has recently been suggested by Tunge et al. that the Fujiwara hydroarylation occurs rather via typical Friedel-Crafts alkenylation pathway; see: J. A. Tunge, L. N. Foresee, Organometallics 2005, 24, 6440.
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    • 6]and water (1:1, v/v), without any metal triflate catalyst. However, no reaction occurred at all.
    • 6]and water (1:1, v/v), without any metal triflate catalyst. However, no reaction occurred at all.
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    • Manuscript in review.
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    • 6] (5 equivs.).
    • 6] (5 equivs.).
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    • 5n+1] as catalysts; manuscript in preparation.
    • 5n+1] as catalysts; manuscript in preparation.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.