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Volumn 86, Issue 7, 2008, Pages 676-681

Asymmetric oxidation of 2-(arylsulfenyl)pyrroles

Author keywords

Asymmetric oxidation; Pyrrole; Sulfide; Sulfoxide

Indexed keywords

CHEMICAL OXYGEN DEMAND; NITROGEN COMPOUNDS; OXIDATION;

EID: 46249093386     PISSN: 00084042     EISSN: None     Source Type: Journal    
DOI: 10.1139/V08-054     Document Type: Article
Times cited : (10)

References (45)
  • 16
    • 46249096985 scopus 로고    scopus 로고
    • K. Matsumoto, T. Yamaguchi, and T. Katsuki. Chem. Conrmun. 1704, (2008).
    • K. Matsumoto, T. Yamaguchi, and T. Katsuki. Chem. Conrmun. 1704, (2008).
  • 26
    • 46249108076 scopus 로고    scopus 로고
    • Caution: in our hands, 2-thiocyanatopyrrole decomposed very readily and was also extremely liable to pass through multiple layers of latex gloves to cause stains and discomfort of the skin
    • Caution: in our hands, 2-thiocyanatopyrrole decomposed very readily and was also extremely liable to pass through multiple layers of latex gloves to cause stains and discomfort of the skin.
  • 29
    • 46249123010 scopus 로고    scopus 로고
    • The asymmetric oxidation of prochiral sulfides presents the opportunity of coupling the initial asymmetric synthesis with a kinetic resolution. While the kinetic resolution of racemic 7a using the Modena protocol (Table 1, entry 8; 30% conversion. 17% ee) revealed a small kinetic preference s, 3, the results in Table 1 indicate that the enantioselectivity occurred predominantly via the initial asymmetric synthesis
    • The asymmetric oxidation of prochiral sulfides presents the opportunity of coupling the initial asymmetric synthesis with a kinetic resolution. While the kinetic resolution of racemic 7a using the Modena protocol (Table 1, entry 8; 30% conversion. 17% ee) revealed a small kinetic preference (s = 3), the results in Table 1 indicate that the enantioselectivity occurred predominantly via the initial asymmetric synthesis.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.