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Volumn 64, Issue 9, 1999, Pages 3335-3338

Novel tandem cyclizations/reaction with electrophiles of α-aminoalkyl radicals

Author keywords

[No Author keywords available]

Indexed keywords

ALKYL GROUP; AMINO ACID;

EID: 0033617399     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo981735d     Document Type: Note
Times cited : (26)

References (38)
  • 25
    • 0000702878 scopus 로고
    • The use of radical cyclizationg in organic synthesis is of increasing importance; see: Jasperse, C. P.; Curran, D. P.; Fevig, T. L. Chem. Rev. 1991, 91, 1237. Samarium diiodide-mediated sequencing reactions have been reviewed recently; see: Molander, G. A.; Harris, C. R. Chem. Rev. 1996, 96, 307. Molander, G. A.; Harris, C. R. Tetrahedron 1998, 54, 3321.
    • (1991) Chem. Rev. , vol.91 , pp. 1237
    • Jasperse, C.P.1    Curran, D.P.2    Fevig, T.L.3
  • 26
    • 2142715741 scopus 로고    scopus 로고
    • The use of radical cyclizationg in organic synthesis is of increasing importance; see: Jasperse, C. P.; Curran, D. P.; Fevig, T. L. Chem. Rev. 1991, 91, 1237. Samarium diiodide-mediated sequencing reactions have been reviewed recently; see: Molander, G. A.; Harris, C. R. Chem. Rev. 1996, 96, 307. Molander, G. A.; Harris, C. R. Tetrahedron 1998, 54, 3321.
    • (1996) Chem. Rev. , vol.96 , pp. 307
    • Molander, G.A.1    Harris, C.R.2
  • 27
    • 0032473838 scopus 로고    scopus 로고
    • The use of radical cyclizationg in organic synthesis is of increasing importance; see: Jasperse, C. P.; Curran, D. P.; Fevig, T. L. Chem. Rev. 1991, 91, 1237. Samarium diiodide-mediated sequencing reactions have been reviewed recently; see: Molander, G. A.; Harris, C. R. Chem. Rev. 1996, 96, 307. Molander, G. A.; Harris, C. R. Tetrahedron 1998, 54, 3321.
    • (1998) Tetrahedron , vol.54 , pp. 3321
    • Molander, G.A.1    Harris, C.R.2
  • 35
    • 0344983033 scopus 로고    scopus 로고
    • note
    • See ref 14c for a related case in the hex-5-enyl radical system. We thank a reviewer for calling this point to our attention.
  • 37
    • 0344552049 scopus 로고    scopus 로고
    • note
    • Secondary carbanions can be prepared from N-(α-aminoalkyl)-benzotriazoles by using the more powerful reducing agent Li/LiBr; see ref 16.
  • 38
    • 0000709398 scopus 로고
    • For a recent survey of the synthesis of pyrrolidines, see: Denmark, S. E.; Marcin, L. R. J. Org. Chem. 1993, 58, 3857.
    • (1993) J. Org. Chem. , vol.58 , pp. 3857
    • Denmark, S.E.1    Marcin, L.R.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.