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Volumn 68, Issue 25, 2003, Pages 9598-9603

A Short Route toward Chiral, Polyhydroxylated Indolizidines and Quinolizidines

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EID: 0345529044     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo0350662     Document Type: Article
Times cited : (63)

References (65)
  • 1
    • 0030787335 scopus 로고    scopus 로고
    • Selected publications on the construction of bicyclic azasugars: (a) Hembre, E. J.; Pearson, W. H. Tetrahedron 1997, 53, 11021-11032.
    • (1997) Tetrahedron , vol.53 , pp. 11021-11032
    • Hembre, E.J.1    Pearson, W.H.2
  • 43
    • 0000012312 scopus 로고
    • Morrison, J. D., Ed.; Academic Press: New York, Chapter 6
    • See for a review of formation of heterocycles by olefin cyclization: Bartlett, P. A. In Asymmetric Synthesis; Morrison, J. D., Ed.; Academic Press: New York, 1984; Vol. 3, Chapter 6.
    • (1984) Asymmetric Synthesis , vol.3
    • Bartlett, P.A.1
  • 44
    • 0029914515 scopus 로고    scopus 로고
    • Some examples of formation of hydroxylated azacycles by iodoamination: (a) Martin, O. R.; Liu, L.; Yang, F. Tetrahedron Lett. 1996, 37, 1991-1994.
    • (1996) Tetrahedron Lett. , vol.37 , pp. 1991-1994
    • Martin, O.R.1    Liu, L.2    Yang, F.3
  • 48
    • 0010671496 scopus 로고
    • Evidence for a the existence of an ethylene/iodine π-complex instead of an iodonium ion as the reactive intermediate in the halocyclization reactions has been reported: Bernett, R. G.; Doi, J. T.; Musker, W. K. J. Org. Chem. 1995, 50, 2048-2050.
    • (1995) J. Org. Chem. , vol.50 , pp. 2048-2050
    • Bernett, R.G.1    Doi, J.T.2    Musker, W.K.3
  • 56
    • 0344990513 scopus 로고    scopus 로고
    • note
    • The atom numbering of the bicyclic structures is depicted below. For convenience, the aziridinium ion was numbered in the same manner as compound 13. (diagram presented)
  • 57
    • 0344559452 scopus 로고    scopus 로고
    • note
    • The same ratio was found after refluxing 13 in DCM for 2 days.
  • 58
    • 0000036407 scopus 로고
    • The involvement of aziridinium inermediates in pyrrolidine to piperidine conversions has been described. See, for example: (a) Logothetis, A. L. J. Am. Chem. Soc. 1965, 87, 749-754.
    • (1965) J. Am. Chem. Soc. , vol.87 , pp. 749-754
    • Logothetis, A.L.1
  • 65
    • 0002406544 scopus 로고
    • See for a review on the preparation and reactions of aziridinium salts: Crist, D. R.; Leonard, N. J. Angew. Chem. 1969, 81, 953-1008.
    • (1969) Angew. Chem. , vol.81 , pp. 953-1008
    • Crist, D.R.1    Leonard, N.J.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.