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Volumn 11, Issue 7, 2009, Pages 1663-1666

Enantioselective route to 5-methyl-And 5,7-dimethyl-6,7-dihydro-sh- dibenz[c,e]azepine: Secondary amines with switchable axial chirality

Author keywords

[No Author keywords available]

Indexed keywords

AMINE; DIBENZAZEPINE DERIVATIVE;

EID: 64349099556     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol900333c     Document Type: Article
Times cited : (38)

References (61)
  • 3
    • 0032999654 scopus 로고    scopus 로고
    • For a correction, see
    • (b) For a correction, see: Berg, U.; Bladh, H. Helv. Chim. Acta 1999, 82, 323.
    • (1999) Helv. Chim. Acta , vol.82 , pp. 323
    • Berg, U.1    Bladh, H.2
  • 8
    • 0037012716 scopus 로고    scopus 로고
    • Ooi, T.; Uematsu, Y.; Kameda, M; Maruoka, K. Ansew. Chem., Int. Ed. 2002, 41, 1551.
    • (c) Ooi, T.; Uematsu, Y.; Kameda, M; Maruoka, K. Ansew. Chem., Int. Ed. 2002, 41, 1551.
  • 38
    • 64349097660 scopus 로고    scopus 로고
    • It is reported (Chem. Abstr. 1988, 108, 625) that the amine (±) -4 was prepared, together with several homologues, in the course of a study into the control of hyperlipidemia: Hall, I. H.; Wyrick, S. D.; Chapman, J. M. U. S. 4689326, 1987. However, the preparative procedure and the NMR data provided in this publication indicate that the compounds prepared were the symmetrical N-alkyl isomers.
    • It is reported (Chem. Abstr. 1988, 108, 625) that the amine (±) -4 was prepared, together with several homologues, in the course of a study into the control of hyperlipidemia: Hall, I. H.; Wyrick, S. D.; Chapman, J. M. U. S. 4689326, 1987. However, the preparative procedure and the NMR data provided in this publication indicate that the compounds prepared were the symmetrical N-alkyl isomers.
  • 41
    • 33746273255 scopus 로고    scopus 로고
    • Joncour, A.; Décor, A.; Thoret, S.; Chiaroni, A.; Baudoin, O. Aneew. Chem. Int. Ed. 2006, 45, 4149.
    • (a) Joncour, A.; Décor, A.; Thoret, S.; Chiaroni, A.; Baudoin, O. Aneew. Chem. Int. Ed. 2006, 45, 4149.
  • 58
    • 27644448390 scopus 로고    scopus 로고
    • For examples in the analogous phosphepine series, see
    • For examples in the analogous phosphepine series, see Kasák, P.; Mereiter, K.; Widhalm, M. Tetrahedron: Asymmetry 2005, 16, 3416.
    • (2005) Tetrahedron: Asymmetry , vol.16 , pp. 3416
    • Kasák, P.1    Mereiter, K.2    Widhalm, M.3
  • 60
    • 64349111575 scopus 로고    scopus 로고
    • H 0.92) is consistent with a pseudoaxial orientation, and therefore an aR-configuration for this compound, indicating that the conformation of the amine 4 can also be modified by N-alkylation.
    • H 0.92) is consistent with a pseudoaxial orientation, and therefore an aR-configuration for this compound, indicating that the conformation of the amine 4 can also be modified by N-alkylation.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.