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Volumn 10, Issue 5, 1999, Pages 1001-1014

Chiral 1,3-diamines from a lithiated isocyanide and chiral aziridines

Author keywords

[No Author keywords available]

Indexed keywords

1,3 DIAMINE; AZIRIDINE DERIVATIVE; DIAMINE; ISOCYANIDE; UNCLASSIFIED DRUG;

EID: 0033548372     PISSN: 09574166     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0957-4166(99)00075-0     Document Type: Article
Times cited : (25)

References (22)
  • 4
    • 0344381211 scopus 로고    scopus 로고
    • note
    • When nucleophilic ring opening of activated aziridines occurs regioselectively at the less substituted side, no racemization is observed, so the enantiomeric purity of the obtained compounds is related to the corresponding starting materials (see Ref. 8).
  • 6
    • 0010698283 scopus 로고
    • Falbe, J., Ed. Thieme: Stuttgart, and references cited therein
    • Grundmann, C. In Houben-Weyl - Methoden der Organischen Chemie; 4th edn; Falbe, J., Ed. Thieme: Stuttgart, 1985; Vol. E5, Teil 2, pp. 1611-1658 and references cited therein.
    • (1985) Houben-Weyl - Methoden der Organischen Chemie; 4th Edn , vol.E5 , Issue.2 TEIL , pp. 1611-1658
    • Grundmann, C.1
  • 8
    • 0000400367 scopus 로고
    • and references cited therein
    • Tanner, D. Angew. Chem. 1994, 106, 625-646 and references cited therein.
    • (1994) Angew. Chem. , vol.106 , pp. 625-646
    • Tanner, D.1
  • 10
    • 0010372191 scopus 로고    scopus 로고
    • and references cited therein
    • So far the tosyl group was the most extensively employed activating group, in recent years other very promising S and P derived activating groups emerged in the literature: (a) Wipf, P.; Venkatraman, S. Synlett 1997, 1-10 and references cited therein. (b) Maligres, P. E.; See, M. M.; Askin, D.; Reider, P. J. Tetrahedron Lett. 1997, 38, 5253-5256. (c) Gajda, T.; Napieraj, A.; Osowska-Pacewicka, K.; Zawadzki, S.; Zwierzak, A. Tetrahedron 1997, 53, 4935-4946.
    • (1997) Synlett , pp. 1-10
    • Wipf, P.1    Venkatraman, S.2
  • 11
    • 0030790051 scopus 로고    scopus 로고
    • So far the tosyl group was the most extensively employed activating group, in recent years other very promising S and P derived activating groups emerged in the literature: (a) Wipf, P.; Venkatraman, S. Synlett 1997, 1-10 and references cited therein. (b) Maligres, P. E.; See, M. M.; Askin, D.; Reider, P. J. Tetrahedron Lett. 1997, 38, 5253-5256. (c) Gajda, T.; Napieraj, A.; Osowska-Pacewicka, K.; Zawadzki, S.; Zwierzak, A. Tetrahedron 1997, 53, 4935-4946.
    • (1997) Tetrahedron Lett. , vol.38 , pp. 5253-5256
    • Maligres, P.E.1    See, M.M.2    Askin, D.3    Reider, P.J.4
  • 12
    • 0030888311 scopus 로고    scopus 로고
    • So far the tosyl group was the most extensively employed activating group, in recent years other very promising S and P derived activating groups emerged in the literature: (a) Wipf, P.; Venkatraman, S. Synlett 1997, 1-10 and references cited therein. (b) Maligres, P. E.; See, M. M.; Askin, D.; Reider, P. J. Tetrahedron Lett. 1997, 38, 5253-5256. (c) Gajda, T.; Napieraj, A.; Osowska-Pacewicka, K.; Zawadzki, S.; Zwierzak, A. Tetrahedron 1997, 53, 4935-4946.
    • (1997) Tetrahedron , vol.53 , pp. 4935-4946
    • Gajda, T.1    Napieraj, A.2    Osowska-Pacewicka, K.3    Zawadzki, S.4    Zwierzak, A.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.