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Volumn , Issue 12, 1997, Pages 1420-1422

Radical cyclization of dialkyldiallylammonium salts. A stereoselective route to pyrrolidines

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Indexed keywords


EID: 0002587057     PISSN: 09365214     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-1997-1043     Document Type: Article
Times cited : (7)

References (40)
  • 23
    • 26844568761 scopus 로고    scopus 로고
    • note
    • 3).
  • 24
    • 26844485442 scopus 로고    scopus 로고
    • note
    • In a blank experiment TsSePh 1 was refluxed in acetonitrile in the presence of TBAI, after 1 h 1 had totally disappeared, if formed TsI was probably decomposed by prolonged heating.
  • 25
    • 85086811928 scopus 로고    scopus 로고
    • note
    • 3 initiation.
  • 28
    • 0001478231 scopus 로고
    • RN1 process (see : Kerber, R. C., Urry, G.W. Kornblum, N. J. Am. Chem. Soc. 1965, 87, 4520). Since dequaternization under the Kornblum conditions is efficient on the parent substrate, the failure possibly originates in the introduction of the selenide or the sulfone groups.
    • (1965) J. Am. Chem. Soc. , vol.87 , pp. 4520
    • Kerber, R.C.1    Urry, G.W.2    Kornblum, N.3
  • 34
    • 0030901690 scopus 로고    scopus 로고
    • For some recent examples of the application of Lewis acids to stereoselective radical transformations, see: (a) Molander, G. A.; McWilliams, J. C.; Noll, B. C. J. Am. Chem. Soc. 1997, 119, 1265.
    • (1997) J. Am. Chem. Soc. , vol.119 , pp. 1265
    • Molander, G.A.1    McWilliams, J.C.2    Noll, B.C.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.