메뉴 건너뛰기




Volumn 25, Issue 7, 2007, Pages 1027-1030

Liquid-phase synthesis of methyl (2Z)-2-arylsulfonylmethyl-2-alkenoates from PEG-supported α-phenylselenopropionate

Author keywords

Liquid phase organic synthesis; Methyl (2Z) 2 arylsulfonylmethyl 2 alkenoates; PEG supported selenopropionate

Indexed keywords


EID: 34548069910     PISSN: 1001604X     EISSN: None     Source Type: Journal    
DOI: 10.1002/cjoc.200790164     Document Type: Article
Times cited : (7)

References (43)
  • 39
    • 0001420970 scopus 로고    scopus 로고
    • 1 H NMR spectrum of a trisubstituted alkene the β-vinylic protons, cis and trans to the ester group are known to resonate at δ=7.5 and δ=6.5, respectively, when the alkene is substituted by an aryl group; while the same protons cis and trans to the ester group appear at δ=6.8 and δ=5.1, respectively, when the alkene is substituted by an alkyl group. See: (a) Larson, G. L.; de Kaifer, C. F.; Seda, R.; Torres, L. E.; Ramirez, J. R. J. Org. Chem. 1984, 49, 3385.
    • 1 H NMR spectrum of a trisubstituted alkene the β-vinylic protons, cis and trans to the ester group are known to resonate at δ=7.5 and δ=6.5, respectively, when the alkene is substituted by an aryl group; while the same protons cis and trans to the ester group appear at δ=6.8 and δ=5.1, respectively, when the alkene is substituted by an alkyl group. See: (a) Larson, G. L.; de Kaifer, C. F.; Seda, R.; Torres, L. E.; Ramirez, J. R. J. Org. Chem. 1984, 49, 3385.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.