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Volumn 33, Issue 13, 1977, Pages 1577-1580

Mechanisms of elimination reactions-XXVI. The α'-β mechanism in elimination reactions of sulforium salts

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EID: 21944444391     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/0040-4020(77)80164-6     Document Type: Article
Times cited : (16)

References (27)
  • 1
    • 84918273247 scopus 로고    scopus 로고
    • This work was supported by the National Science Foundation.
  • 16
    • 0343814002 scopus 로고
    • Stereochemical studies. XLIV. The syn-anti elimination dichotomy - A general feature in cycloalkene formation from 'onium salts in protic solvents
    • Rates for the sulfonium salts are not available, but the corresponding ammonium salts show elimination rates up to 20 times faster (with t-BuOK/t-BuOH) for the cyclopentyl than for the cyclohexyl derivatives
    • (1967) Collection of Czechoslovak Chemical Communications , vol.32 , pp. 3701
    • Závada1    Sicher2
  • 18
    • 37049136331 scopus 로고
    • Mechanisms of elimination reactions. The effect of added dimethyl sulphoxide on rates, isotope effects, and substituent effects in the reaction of 2-arylethyldimethylsulphonium bromides with sodium hydroxide in water
    • (1967) Journal of the Chemical Society B: Physical Organic , pp. 964
    • Cockerill1
  • 19
    • 84918273245 scopus 로고    scopus 로고
    • Ref. 3, Chap. III.
  • 20
    • 84918273244 scopus 로고    scopus 로고
    • Reproducibility of this number is poor, probably because of difficulty in integrating the NMR peak of the methinyl proton. The extent of exchange is, if anything, probably greater than the figures indicate.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.