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Volumn 8, Issue 7, 2010, Pages 1712-1717

Nucleophilic attack of 2-sulfinyl acrylates: A mild and general approach to sulfenic acid anions

Author keywords

[No Author keywords available]

Indexed keywords

GENERAL APPROACH; NUCLEOPHILIC ATTACK; STEREOSPECIFICITY; SULFENIC ACIDS; THIOLATES;

EID: 77949812795     PISSN: 14770520     EISSN: None     Source Type: Journal    
DOI: 10.1039/b917217c     Document Type: Article
Times cited : (25)

References (32)
  • 20
    • 12344308233 scopus 로고    scopus 로고
    • The lowest yields were incurred with methyl compound 2b, partially due to volatility concerns. For full details, see the ESI
    • R. J. Faragher D. Alberico A. L. Schwan Tetrahedron 2005 61 1115 1125
    • (2005) Tetrahedron , vol.61 , pp. 1115-1125
    • Faragher, R.J.1    Alberico, D.2    Schwan, A.L.3
  • 23
    • 24144449924 scopus 로고    scopus 로고
    • Experiments with benzyl sulfenate and phenyl sulfenate show that decomposition of the sulfenate occurs as the temperature of the reaction approaches 0°C if no electrophile is present Prof. Stephane Perrio, private communication, June 10, 2009
    • M. C. Aversa A. Barattucci M. C. Bilardo P. Bonaccorsi P. Giannetto P. Rollin A. Tatibouet J. Org. Chem. 2005 70 7389 7396
    • (2005) J. Org. Chem. , vol.70 , pp. 7389-7396
    • Aversa, M.C.1    Barattucci, A.2    Bilardo, M.C.3    Bonaccorsi, P.4    Giannetto, P.5    Rollin, P.6    Tatibouet, A.7
  • 32
    • 0033607626 scopus 로고    scopus 로고
    • The elimination reaction represents an accelerated analog of the common thermally induced syn cycloelimination of sulfenic acid from sulfoxides bearing one or more β-hydrogens
    • F. A. Davis H. Liu C.-H. Liang G. V. Reddy Y. Zhang T. Fang D. D. Titus J. Org. Chem. 1999 64 8929 8935
    • (1999) J. Org. Chem. , vol.64 , pp. 8929-8935
    • Davis, F.A.1    Liu, H.2    Liang, C.-H.3    Reddy, G.V.4    Zhang, Y.5    Fang, T.6    Titus, D.D.7


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.