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Volumn , Issue 8, 1999, Pages 1191-1199

Iodocarbocyclization and iodoaminocyclization reactions mediated by a metallic reagent

Author keywords

Catalytic asymmetric reaction; Iodine; Iodoaminocyclization; Iodocarbocyclization; Metallic reagent

Indexed keywords

REAGENT;

EID: 0032769887     PISSN: 09365214     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-1999-2790     Document Type: Article
Times cited : (70)

References (50)
  • 1
    • 0000012312 scopus 로고
    • Ed. Morrison, J. D. Academic Press, Orland
    • For reviews of halocyclization, see: (a) Bartlett, P. A. In Asymmetric Synthesis, Ed. Morrison, J. D. Academic Press, Orland, 1984, Vol. 3, p411.
    • (1984) Asymmetric Synthesis , vol.3 , pp. 411
    • Bartlett, P.A.1
  • 3
    • 0001329983 scopus 로고
    • Eds. Trost, B. M. Fleming, I. Pergamon Press, New York
    • (c) Harding, K. E.; Tiner, T. H. In Comprehensive Organic Synthesis, Eds. Trost, B. M. Fleming, I. Pergamon Press, New York, 1991, Vol. 4, p363.
    • (1991) Comprehensive Organic Synthesis , vol.4 , pp. 363
    • Harding, K.E.1    Tiner, T.H.2
  • 12
    • 0026697770 scopus 로고
    • 2 and NaI at high temperature to give iodoalkylcyclopropane or cyclopentane derivatives. However, under their reaction conditions, mixtures of cyclized products and α-iodomalonates are often obtained. Beckwith, A. L.; Zozer, M. J. Tetrahedron Lett. 1992, 33, 4975.
    • (1992) Tetrahedron Lett. , vol.33 , pp. 4975
    • Beckwith, A.L.1    Zozer, M.J.2
  • 37
    • 0344591030 scopus 로고    scopus 로고
    • note
    • 3, the decthoxycabonylated reaction hardly proceeded.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.