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Volumn 21, Issue 4, 2010, Pages 382-384

The first example of racemization of the sulfur stereogenic center of α-sulfinyl carbanions at low temperatures

Author keywords

[No Author keywords available]

Indexed keywords

ALKALI; BASE; SULFOXIDE; TETRAHYDROFURAN; TRIMETHYLSILYL DERIVATIVE;

EID: 77951023512     PISSN: 09574166     EISSN: 1362511X     Source Type: Journal    
DOI: 10.1016/j.tetasy.2010.02.013     Document Type: Article
Times cited : (12)

References (30)
  • 1
    • 0004139460 scopus 로고
    • Some selected recent books and reviews concerning chemistry, synthesis, and synthetic uses of optically active sulfoxides:. Patai S., and Rappoport Z. (Eds), John Wiley and Sons, Chichester
    • Some selected recent books and reviews concerning chemistry, synthesis, and synthetic uses of optically active sulfoxides:. In: Patai S., and Rappoport Z. (Eds). The Chemistry of Sulphones and Sulphoxides (1988), John Wiley and Sons, Chichester
    • (1988) The Chemistry of Sulphones and Sulphoxides
  • 13
    • 13844266440 scopus 로고    scopus 로고
    • Some selected recent papers for asymmetric synthesis using enantiopure 1-chloroalkyl p-tolyl sulfoxides from our laboratories:
    • Some selected recent papers for asymmetric synthesis using enantiopure 1-chloroalkyl p-tolyl sulfoxides from our laboratories:. Sugiyama S., and Satoh T. Tetrahedron: Asymmetry 16 (2005) 665
    • (2005) Tetrahedron: Asymmetry , vol.16 , pp. 665
    • Sugiyama, S.1    Satoh, T.2
  • 21
    • 57149143467 scopus 로고    scopus 로고
    • Rappoport Z., and Marek I. (Eds), John Wiley and Sons, Chichester
    • Satoh T. In: Rappoport Z., and Marek I. (Eds). The Chemistry of Organomagnesium Compounds (2008), John Wiley and Sons, Chichester 717-769
    • (2008) The Chemistry of Organomagnesium Compounds , pp. 717-769
    • Satoh, T.1
  • 24
    • 34250005744 scopus 로고    scopus 로고
    • Some new synthetic methods by using aryl dichloromethyl sulfoxide from our laboratories:
    • Some new synthetic methods by using aryl dichloromethyl sulfoxide from our laboratories:. Miyagawa T., and Satoh T. Tetrahedron Lett. 48 (2007) 4849
    • (2007) Tetrahedron Lett. , vol.48 , pp. 4849
    • Miyagawa, T.1    Satoh, T.2
  • 29
    • 77951022359 scopus 로고    scopus 로고
    • note
    • A solution of (R)-1a in THF was added to a solution of LDA in THF at -78 °C.
  • 30
    • 77951022100 scopus 로고    scopus 로고
    • note
    • The enantiomeric excess of 1a was easily determined by HPLC with a chiral stationary column, CHIRALCEL OD.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.