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Volumn 84, Issue 11, 2011, Pages 1248-1250

Diphenyl diselenide-assisted α-phenylthiolation of carbonyl compounds with diphenyl disulfide

Author keywords

[No Author keywords available]

Indexed keywords

CATALYTIC AMOUNTS; DIPHENYL DISELENIDE; DIPHENYL DISULFIDE; PHENYLTHIO;

EID: 81255166005     PISSN: 00092673     EISSN: 13480634     Source Type: Journal    
DOI: 10.1246/bcsj.20110127     Document Type: Article
Times cited : (5)

References (28)
  • 1
    • 33947092148 scopus 로고
    • For reviews on a-phenylthio carbonyl compounds, see: B. M. Trost, Chem. Rev. 1978, 78, 363.
    • (1978) Chem. Rev. , vol.78 , pp. 363
    • Trost, B.M.1
  • 3
    • 84982475844 scopus 로고
    • D. Scholz, Chem. Ber. 1981, 114, 909, and references cited therein.
    • (1981) Chem. Ber. , vol.114 , pp. 909
    • Scholz, D.1
  • 19
    • 0032546285 scopus 로고    scopus 로고
    • Ogawa, Sonoda, et al. have reported the results on the PhSeSePh-assisited dithiolation of 1,3-dienes with PhSSPh upon irradiation with near-UV light, see: A. Ogawa, R. Obayashi, N. Sonoda, T. Hirao, Tetrahedron Lett. 1998, 39, 1577.
    • (1998) Tetrahedron Lett. , vol.39 , pp. 1577
    • Ogawa, A.1    Obayashi, R.2    Sonoda, N.3    Hirao, T.4
  • 20
    • 81255184736 scopus 로고    scopus 로고
    • Under an atmosphere of N2, the yield of 3a (12%) was dramatically decreased
    • Under an atmosphere of N2, the yield of 3a (12%) was dramatically decreased.
  • 21
    • 81255136580 scopus 로고    scopus 로고
    • the absence of CS2CO3, the reaction did not proceed and 4-phenylseleno-5-nonanone was recoverd in almost quantitatively yield
    • In the absence of CS2CO3, the reaction did not proceed and 4-phenylseleno-5-nonanone was recoverd in almost quantitatively yield.
  • 22
    • 81255158424 scopus 로고    scopus 로고
    • R. M. Coates et al. have measured the position of equilibrium established between lithium enolate of cyclohexanone and 2-phenylthiocyclohexanone. See Ref. 3a
    • R. M. Coates et al. have measured the position of equilibrium established between lithium enolate of cyclohexanone and 2-phenylthiocyclohexanone. See Ref. 3a.
  • 23
    • 81255158423 scopus 로고    scopus 로고
    • It is reported that the introducing of phenylthio group at a-position increases the acidity of cyclohexanone by at least 3 pKR units, see Ref. 3a
    • It is reported that the introducing of phenylthio group at a-position increases the acidity of cyclohexanone by at least 3 pKR units, see Ref. 3a.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.