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Volumn 9, Issue 12, 1998, Pages 2093-2099

Application of phosphorylated reagents derived from N,N'-di-[(S)-α- phenylethyl]-cyclohexane-1,2-diamines in the determination of the enantiomeric purity of chiral alcohols

Author keywords

[No Author keywords available]

Indexed keywords

ALCOHOL; CYCLOHEXANE 1,2 DIAMINE; UNCLASSIFIED DRUG;

EID: 0032547126     PISSN: 09574166     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0957-4166(98)00219-5     Document Type: Article
Times cited : (38)

References (30)
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    • (a) For a detailed recent review, see: Parker, D. Chem. Rev. 1991, 91, 1441.
    • (1991) Chem. Rev. , vol.91 , pp. 1441
    • Parker, D.1
  • 17
    • 0011249494 scopus 로고
    • For other chiral derivatizing agents based on enantiopure trans-1,2-diaminocyclohexane, see: (a) Resch, J. F.; Meinwald, J. Tetrahedron Lett. 1981, 22, 3159. (b) Staubach, B.; Buddrus, J. Angew. Chem., Int. Ed. Engl. 1996, 35, 1344.
    • (1981) Tetrahedron Lett. , vol.22 , pp. 3159
    • Resch, J.F.1    Meinwald, J.2
  • 18
    • 0029791250 scopus 로고    scopus 로고
    • For other chiral derivatizing agents based on enantiopure trans-1,2-diaminocyclohexane, see: (a) Resch, J. F.; Meinwald, J. Tetrahedron Lett. 1981, 22, 3159. (b) Staubach, B.; Buddrus, J. Angew. Chem., Int. Ed. Engl. 1996, 35, 1344.
    • (1996) Angew. Chem., Int. Ed. Engl. , vol.35 , pp. 1344
    • Staubach, B.1    Buddrus, J.2
  • 20
    • 0000511992 scopus 로고
    • See, also: (a) Pracejus, H.; Pracejus, G.; Costisella, B. J. Prak. Chem. 1987, 329, 235. (b) Overman, L. E.; Sugai, S. J. Org. Chem. 1985, 50, 4154. Barbara, P.; Bianchini, C.; Sernau, V. Tetrahedron: Asymmetry 1996, 7, 843.
    • (1987) J. Prak. Chem. , vol.329 , pp. 235
    • Pracejus, H.1    Pracejus, G.2    Costisella, B.3
  • 21
    • 0001464408 scopus 로고
    • See, also: (a) Pracejus, H.; Pracejus, G.; Costisella, B. J. Prak. Chem. 1987, 329, 235. (b) Overman, L. E.; Sugai, S. J. Org. Chem. 1985, 50, 4154. Barbara, P.; Bianchini, C.; Sernau, V. Tetrahedron: Asymmetry 1996, 7, 843.
    • (1985) J. Org. Chem. , vol.50 , pp. 4154
    • Overman, L.E.1    Sugai, S.2
  • 22
    • 0029928591 scopus 로고    scopus 로고
    • See, also: (a) Pracejus, H.; Pracejus, G.; Costisella, B. J. Prak. Chem. 1987, 329, 235. (b) Overman, L. E.; Sugai, S. J. Org. Chem. 1985, 50, 4154. Barbara, P.; Bianchini, C.; Sernau, V. Tetrahedron: Asymmetry 1996, 7, 843.
    • (1996) Tetrahedron: Asymmetry , vol.7 , pp. 843
    • Barbara, P.1    Bianchini, C.2    Sernau, V.3
  • 25
    • 0000567366 scopus 로고
    • Trost, B. M.; Fleming, I., Eds.; Pergamon Press: Oxford
    • For a general discussion on aziridine conversion to 1,2-diamines, see: Kemp, J. E. G. In Comprehensive Organic Synthesis; Trost, B. M.; Fleming, I., Eds.; Pergamon Press: Oxford, 1991, Vol. 7, p. 469.
    • (1991) Comprehensive Organic Synthesis , vol.7 , pp. 469
    • Kemp, J.E.G.1
  • 26
    • 0345176677 scopus 로고    scopus 로고
    • 13 The present application to aziridine ring opening may prove to be a valuable synthetic method
    • 13 The present application to aziridine ring opening may prove to be a valuable synthetic method.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.