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Volumn 56, Issue 16, 2000, Pages 2339-2358

Nitrogen protecting groups: Recent developments and new applications

Author keywords

[No Author keywords available]

Indexed keywords

ACID; ALPHA METHYLBENZYLAMINE; FUNCTIONAL GROUP; HYDRAZINE DERIVATIVE; NITROGEN; OXAZIRIDINE DERIVATIVE; POLYAMINE; SODIUM IODIDE;

EID: 0034647015     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4020(99)00980-1     Document Type: Review
Times cited : (75)

References (124)
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  • 29
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    • Natural Polyamine Derivatives: New Aspects of Their Isolation, Structure Elucidation and Synthesis
    • G. Cordell, Brossi A. Orlando: Academic Press
    • Guggisberg A., Hesse M. Natural Polyamine Derivatives: New Aspects of Their Isolation, Structure Elucidation and Synthesis. Cordell G., Brossi A. The Alkaloids. Vol. 50:1998;219-256 Academic Press, Orlando.
    • (1998) The Alkaloids , vol.50 , pp. 219-256
    • Guggisberg, A.1    Hesse, M.2
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    • 0033524651 scopus 로고    scopus 로고
    • N-Tosyl gave better results, such as efficiency of catalyst and a smoother reaction, than the N-benzyl analogs in the copper-catalyzed reactions involving γ-lactams
    • N-Tosyl gave better results, such as efficiency of catalyst and a smoother reaction, than the N-benzyl analogs in the copper-catalyzed reactions involving γ-lactams. Iwamatsu, S.; Kondo, H.; Matsubara, K.; Nagashima, H. Tetrahedron 1999, 55, 1687.
    • (1999) Tetrahedron , vol.55 , pp. 1687
    • Iwamatsu, S.1    Kondo, H.2    Matsubara, K.3    Nagashima, H.4
  • 71
    • 0000346930 scopus 로고
    • First asymmetric synthesis of (-)-pinidine, and (+)-pinidine by
    • First asymmetric synthesis of (-)-pinidine, and (+)-pinidine by Yamazaki, N.; Kibayashi, C. J. Am. Chem. Soc. 1989, 111, 1396.
    • (1989) J. Am. Chem. Soc. , vol.111 , pp. 1396
    • Yamazaki, N.1    Kibayashi, C.2
  • 85
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    • (a) Boche, G. In Houben-Weyl, Methods of Organic Chemistry; Helmchen, G.; Hoffmann, R. W.; Multzer, J.; Schaumann, E., Eds.; Thieme Verlag: Stuttgart, Vol. E, 21e, Stereoselective Synthesis, 1995; p 5133.
    • Methods of Organic Chemistry , vol.E
    • Boche, G.1
  • 86
    • 0004005454 scopus 로고
    • (a) Boche, G. In Houben-Weyl, Methods of Organic Chemistry; Helmchen, G.; Hoffmann, R. W.; Multzer, J.; Schaumann, E., Eds.; Thieme Verlag: Stuttgart, Vol. E, 21e, Stereoselective Synthesis, 1995; p 5133.
    • (1995) Stereoselective Synthesis , pp. 5133
  • 93
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    • (a)
    • (a) Enders, D.; Lohray, B. B. Angew. Chem. 1987, 99, 359. Angew. Chem., Int. Ed. Engl. 1987, 26, 351.
    • (1987) Angew. Chem. , vol.99 , pp. 359
    • Enders, D.1    Lohray, B.B.2
  • 94
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.