메뉴 건너뛰기




Volumn 53, Issue 36, 1997, Pages 12147-12158

Chemoselective reduction of organoselenocyanates to diselenides and selenolates

Author keywords

[No Author keywords available]

Indexed keywords

ORGANOSELENIUM DERIVATIVE; SELENIDE;

EID: 0030759875     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4020(97)00548-6     Document Type: Article
Times cited : (56)

References (63)
  • 1
    • 0342476559 scopus 로고
    • Schwefel-, selen-, tellur-verbindungen
    • Müller, E. ed., Georg Thieme Verlag, Stuttgart
    • (a) Rheinboldt, H. in 'Schwefel-, Selen-, Tellur-Verbindungen', Methoden der Organische Chemie (Houben Weyl) Müller, E. ed., Georg Thieme Verlag, Stuttgart, 1967, vol. 9.
    • (1967) Methoden der Organische Chemie (Houben Weyl) , vol.9
    • Rheinboldt, H.1
  • 4
    • 0002197080 scopus 로고
    • Patai, S. ; Rappoport, Z. eds., John Wiley and Sons, Chichester, Chap 3
    • (d) Back, T. J. in 'The Chemistry of Organic Selenium and Tellurium Compounds', Patai, S. ; Rappoport, Z. eds., John Wiley and Sons, Chichester, 1987, vol. 2, Chap 3, pp 91
    • (1987) The Chemistry of Organic Selenium and Tellurium Compounds , vol.2 , pp. 91
    • Back, T.J.1
  • 15
    • 0342476529 scopus 로고    scopus 로고
    • Chemoselective reactions of prim- and sec-Alcohols with phenylselenocyanate : Efficient syntheses of alkanes and alkenes and stereoselective synthesis of alkylbromides with retention of configuration
    • March
    • (a) Krief, A. in 'Chemoselective Reactions of prim- and sec-Alcohols with Phenylselenocyanate : Efficient Syntheses of Alkanes and Alkenes and Stereoselective Synthesis of Alkylbromides with Retention of Configuration' Acros Info Sheet No 16, 1996, March
    • (1996) Acros Info Sheet No 16 , vol.16
    • Krief, A.1
  • 16
    • 0342476530 scopus 로고    scopus 로고
    • 2-Nitrophenylselenocyanate : The grieco-sharpless olefination reaction
    • May
    • (b) Krief, A. in '2-Nitrophenylselenocyanate : The Grieco-Sharpless Olefination Reaction' Acros Info Sheet No 17, 1996, May.
    • (1996) Acros Info Sheet No 17 , vol.17
    • Krief, A.1
  • 53
    • 0342428674 scopus 로고    scopus 로고
    • note
    • (b) This product is commercialized by Acros : Janssen Pharmaceuticalaan 3, 2440 Geel, Belgium.
  • 61
    • 33947435055 scopus 로고
    • reaction performed in ethanol, butyl selenocyanate : 44% yield; decyl selenocyanate : 67 % yield
    • Waever, W. E.; Whaley, W. M. J. Am. Chem. Soc. 1946, 68, 2115 (reaction performed in ethanol, butyl selenocyanate : 44% yield; decyl selenocyanate : 67 % yield).
    • (1946) J. Am. Chem. Soc. , vol.68 , pp. 2115
    • Waever, W.E.1    Whaley, W.M.2
  • 63
    • 33845278370 scopus 로고
    • For a leading reference for the synthesis of alkyl selenocyanates see also: Melnke, P. T.; Kraft, G. A. J. Am. Chem. Soc. 1988, 110, 8671.
    • (1988) J. Am. Chem. Soc. , vol.110 , pp. 8671
    • Meinke, P.T.1    Kraft, G.A.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.