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Volumn 45, Issue 7, 2004, Pages 1469-1471

Ruthenium-catalyzed addition of sulfenamides to alkynes leading to selective synthesis of polyfunctional alkenes

Author keywords

Addition; Alkyne; Polyfunctional alkene; Ruthenium catalyst; Sulfenamide

Indexed keywords

ALKENE DERIVATIVE; ALKYNE DERIVATIVE; POLYFUNCTIONAL GROUP; RUTHENIUM; SULFENAMIDE DERIVATIVE;

EID: 1642578963     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2003.12.025     Document Type: Article
Times cited : (27)

References (17)
  • 3
    • 0000569496 scopus 로고
    • G. Wilkinson, R.D. Gillard, McCleverty J.A. Oxford, UK: Pergamon
    • Hutton A.T. Wilkinson G., Gillard R.D., McCleverty J.A. Comprehensive Coordination Chemistry. Vol. 5:1987;1131-1155 Pergamon, Oxford, UK.
    • (1987) Comprehensive Coordination Chemistry , vol.5 , pp. 1131-1155
    • Hutton, A.T.1
  • 7
    • 0001518970 scopus 로고
    • In a pioneering study by Ogawa and Sonoda et al., the first transition-metal complex-catalyzed addition and carbonylative addition reactions of organic disulfides to terminal alkynes have already been reported.
    • In a pioneering study by Ogawa and Sonoda et al., the first transition-metal complex-catalyzed addition and carbonylative addition reactions of organic disulfides to terminal alkynes have already been reported. Kuniyasu H., Ogawa A., Miyazaki S., Ryu I., Kambe N., Sonoda N. J. Am. Chem. Soc. 113:1991;9796-9803.
    • (1991) J. Am. Chem. Soc. , vol.113 , pp. 9796-9803
    • Kuniyasu, H.1    Ogawa, A.2    Miyazaki, S.3    Ryu, I.4    Kambe, N.5    Sonoda, N.6
  • 11
    • 85030906760 scopus 로고    scopus 로고
    • note
    • 13C NMR data with those of 3a and 3f . The details will be reported in a full paper.
  • 16
    • 0000194075 scopus 로고
    • Selenenamides instead of sulfenamides smoothly reacted with good Michael acceptors such as enones in chloroform without metal catalysts to form α-seleno-β-amino carbonyl compounds. For example, see:
    • Selenenamides instead of sulfenamides smoothly reacted with good Michael acceptors such as enones in chloroform without metal catalysts to form α-seleno-β-amino carbonyl compounds. For example, see: Reich H.J., Renga J.M. J. Org. Chem. 40:1975;3313-3314.
    • (1975) J. Org. Chem. , vol.40 , pp. 3313-3314
    • Reich, H.J.1    Renga, J.M.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.