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Volumn 46, Issue 1, 2005, Pages 69-74

Alkynylation of N-tosylimines with aryl acetylenes promoted by ZnBr 2 and N,N-diisopropylethylamine in acetonitrile

Author keywords

Alkynylation; Aryl acetylenes; DIEA; N Tosylimines; ZnBr 2

Indexed keywords

ACETONITRILE; ACETYLENE DERIVATIVE; AMINE; ETHYLDIISOPROPYLAMINE; IMINE; UNCLASSIFIED DRUG; ZINC BROMIDE;

EID: 9944241364     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2004.11.046     Document Type: Article
Times cited : (60)

References (66)
  • 14
    • 2442517535 scopus 로고    scopus 로고
    • For the alkynylation reaction using acetylide, which was generated by the action of strong base including n-BuLi, EtMgBr, benzyltrimethylammonium hydroxide, or cesium hydroxide, see: T. Murai, Y. Mutoh, Y. Ohta, and M. Murakami J. Am. Chem. Soc. 126 2004 5968
    • (2004) J. Am. Chem. Soc. , vol.126 , pp. 5968
    • Murai, T.1    Mutoh, Y.2    Ohta, Y.3    Murakami, M.4
  • 25
    • 2942596792 scopus 로고    scopus 로고
    • For the related alkynylation reaction using similar approach, see: S. Shahi, and K. Koide Angew. Chem., Int. Ed. 43 2004 2525
    • (2004) Angew. Chem., Int. Ed. , vol.43 , pp. 2525
    • Shahi, S.1    Koide, K.2
  • 37
    • 0037157090 scopus 로고    scopus 로고
    • For the enantioselective alkynylation of aldehydes or aldimines, see: C. Wei, and C.-J. Li J. Am. Chem. Soc. 124 2002 5638
    • (2002) J. Am. Chem. Soc. , vol.124 , pp. 5638
    • Wei, C.1    Li, C.-J.2
  • 63
    • 9944222289 scopus 로고    scopus 로고
    • note
    • 3) δ 21.65, 21.66, 50.03, 85.01, 87.05, 119.10, 127.56, 127.75, 128.63, 128.89, 129.06, 129.76, 131.68, 137.63, 137.77, 138.97, 143.70
  • 64
    • 9944224019 scopus 로고    scopus 로고
    • note
    • +, 26)
  • 65
    • 9944266034 scopus 로고    scopus 로고
    • note
    • +, 2)
  • 66
    • 9944249372 scopus 로고    scopus 로고
    • note
    • +, 7)


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.