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Volumn 38, Issue 31, 1997, Pages 5559-5562

Facile conversion of sulfilimines into sulfoximines using dioxiranes

Author keywords

Dioxiranes; Oxidation; Sulfilimines; Sulfoximines

Indexed keywords

ETHYLENE OXIDE DERIVATIVE; IMINE; REAGENT; SULFIDE; SULFILIMINE DERIVATIVE; SULFOXIDE; SULFOXIMINE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 0030758515     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(97)01243-4     Document Type: Article
Times cited : (18)

References (28)
  • 1
    • 0003417469 scopus 로고    scopus 로고
    • Trost, B. M.; Fleming, I.; Schreiber, S. L., Eds.; Pergamon: Oxford, U.K.
    • (a) Ogura, K. in Comprehensive Organic Synthesis; Trost, B. M.; Fleming, I.; Schreiber, S. L., Eds.; Pergamon: Oxford, U.K. (1991); vol. 1, pp 531-537, and references therein.
    • Comprehensive Organic Synthesis
    • Ogura, K.1
  • 2
    • 0342664636 scopus 로고    scopus 로고
    • and references therein
    • (a) Ogura, K. in Comprehensive Organic Synthesis; Trost, B. M.; Fleming, I.; Schreiber, S. L., Eds.; Pergamon: Oxford, U.K. (1991); vol. 1, pp 531-537, and references therein.
    • Comprehensive Organic Synthesis , vol.1 , pp. 531-537
  • 13
    • 0001218439 scopus 로고
    • Ando, W., Ed.; Wiley, New York, Chapter 4, See also references therein
    • (b) Adam. W.; Hadjiarapoglou, L. P.; Curci, R.; Mello, R. in Organic Peroxides; Ando, W., Ed.; Wiley, New York, 1992 ; Chapter 4, pp 195-219. See also references therein.
    • (1992) Organic Peroxides , pp. 195-219
    • Adam, W.1    Hadjiarapoglou, L.P.2    Curci, R.3    Mello, R.4
  • 19
    • 0342664633 scopus 로고    scopus 로고
    • note
    • 2S: C, 40.25; H, 7.43; N, 9.39. Found: C, 40.01; H, 7.33; N, 9.46.
  • 21
    • 0342664630 scopus 로고    scopus 로고
    • note
    • 1H NMR identical with that of racemic 2d.
  • 23
    • 0343534855 scopus 로고    scopus 로고
    • note
    • 1H NMR identical with that of racemic 2d (cf., ref. 10b reporting the characteristics of optically pure material); its enantiomeric excess was determined as 80% by HPLC of the reaction mixture, employing a chiral stationary phase (DAICEL Chiralcel OD, 25 cm × 0.46 cm ID.; 30% EtOH /70% n-hexane, 1 mL/min).
  • 26
    • 0000451238 scopus 로고
    • Swern, D. , Ed.; Wiley-Interscience, New York, Chapt. 4, and references therein
    • (a) Curci, R.; Edwards, J.O., in Organic Peroxides; Swern, D. , Ed.; Wiley-Interscience, New York, 1970; Vol, I; Chapt. 4, pp. 199-267, and references therein.
    • (1970) Organic Peroxides , vol.1 , pp. 199-267
    • Curci, R.1    Edwards, J.O.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.