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Volumn 59, Issue 2, 2003, Pages 187-196

Regioselective free radical phenylsulfenation of a non-activated δ-carbon atom by the photolysis of alkyl benzenesulfenate

Author keywords

1,5 hydrogen migration; Intramolecular fuctionalization; Radicals and radical reactions; Sulfenic acids and derivatives; Sulfides; phenylthio alcohols

Indexed keywords

ALCOHOL DERIVATIVE; BENZENESULFENATE; CARBON; FREE RADICAL; UNCLASSIFIED DRUG;

EID: 0037421130     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4020(02)01477-1     Document Type: Article
Times cited : (9)

References (56)
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    • 1 H NMR spectrum of the mixture of isomers 15 two signals were obtained for hydrogens next to the phenylthio group, signals at δ=2.84 ppm belong to the trans-isomer 15a and at δ=3.50 ppm are from the cis-isomer 15b and they possess different coupling constants. This is in agreement with described results. Eliel, E.; Wilen, S. H. Stereochemistry of Organic Compounds; Wiley: New York, 1994, pp 712.
    • 1 H NMR spectrum of the mixture of isomers 15 two signals were obtained for hydrogens next to the phenylthio group, signals at δ=2.84 ppm belong to the trans-isomer 15a and at δ=3.50 ppm are from the cis-isomer 15b and they possess different coupling constants. This is in agreement with described results. Eliel, E.; Wilen, S. H. Stereochemistry of Organic Compounds; Wiley: New York, 1994, pp 712.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.