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Volumn 12, Issue 20, 2010, Pages 4454-4457

Regio- and enantioselective iridium-catalyzed allylation of thiophenol: Synthesis of enantiopure allyl phenyl sulfides

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EID: 77957830414     PISSN: 15237060     EISSN: 15237052     Source Type: Journal    
DOI: 10.1021/ol101915b     Document Type: Article
Times cited : (47)

References (43)
  • 34
    • 77957827780 scopus 로고    scopus 로고
    • Various alkali-metal (Li, Na, and K) salts of thiophenol were tested, and we found that sodium thiophenoxide 3 gave the best result.
    • Various alkali-metal (Li, Na, and K) salts of thiophenol were tested, and we found that sodium thiophenoxide 3 gave the best result.
  • 39
    • 77957855756 scopus 로고    scopus 로고
    • The ligand (R, Ra)- 1e was effective in improving the enantioselectivity of the branched product in the Ir-catalyzed o -chlorophenylallylation of indole as indicated in reference 1h.
    • The ligand (R, Ra)- 1e was effective in improving the enantioselectivity of the branched product in the Ir-catalyzed o -chlorophenylallylation of indole as indicated in reference 1h.
  • 40
    • 0028065095 scopus 로고
    • Compound 4j has been prepared in racemic form from 2j by Pd-catalyzed allylation of thiophenol; the yield was very low due to the unfavorable regioselectivity.
    • Compound 4j has been prepared in racemic form from 2j by Pd-catalyzed allylation of thiophenol; the yield was very low due to the unfavorable regioselectivity. Goux, C.; Lhoste, P.; Sinou, D. Tetrahedron 1994, 50, 10321-10330
    • (1994) Tetrahedron , vol.50 , pp. 10321-10330
    • Goux, C.1    Lhoste, P.2    Sinou, D.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.