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Volumn 91, Issue 22, 1995, Pages 2871-2876

Synthesis of chiral diferrocenyl dichalcogenides and their application to asymmetric nucleophilic ring opening of meso-epoxides

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EID: 37049070181     PISSN: 02601826     EISSN: None     Source Type: Journal    
DOI: 10.1039/p19950002871     Document Type: Article
Times cited : (43)

References (18)
  • 5
    • 84944212321 scopus 로고    scopus 로고
    • (up to 50% de) with chiral binaphthylselenium compounds has been reported
    • Diastereoselective ring-opening of cyclohexene oxide (up to 50% de) with chiral binaphthylselenium compounds has been reported:
    • Diastereoselective Ring-Opening of Cyclohexene Oxide.
  • 7
    • 0027451863 scopus 로고
    • Diastereoselective Michael-addition of chiral binaphthyltellurium compounds to enones (up to 70% de) has been reported
    • Diastereoselective Michael-addition of chiral binaphthyltellurium compounds to enones (up to 70% de) has been reported: M. Irie, Y. Doi, M. Ohsuka, Y. Aso, T. Otsubo and F. Ogura. Tetrahedron: Asymmetry, 1993. 4, 2127.
    • (1993) Tetrahedron: Asymmetry. , vol.4 , pp. 2127
    • Irie, M.1    Doi, Y.2    Ohsuka, M.3    Aso, Y.4    Otsubo, T.5    Ogura, F.6
  • 16
    • 0001465047 scopus 로고
    • Selenoxide elimination of the β-hydroxy selenide giving directly cyclohex-2-enol did not proceed
    • Selenoxide elimination of the β-hydroxy selenide giving directly cyclohex-2-enol did not proceed: M. R. Detty. J. Org. Chem., 1980. 45. 274;
    • (1980) J. Org. Chem. , vol.45 , pp. 274
    • Detty, M.R.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.