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Volumn 70, Issue 19, 2005, Pages 7780-7783

New polycyclic diamine scaffolds from dimerization of 3-alkyl-1,4- dihydropyridines in acidic medium

Author keywords

[No Author keywords available]

Indexed keywords

DERIVATIVES; DIMERIZATION; MOLECULES; OXIDATION; REDUCTION; SCAFFOLDS;

EID: 24944536143     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo050937o     Document Type: Article
Times cited : (8)

References (16)
  • 1
    • 0036012737 scopus 로고    scopus 로고
    • and references therein
    • For dihydropyridine chemistry reviews, see: Lavilla, R. J. Chem. Soc., Perkin Trans. 1 2002, 1141-1156 and references therein.
    • (2002) J. Chem. Soc., Perkin Trans. 1 , pp. 1141-1156
    • Lavilla, R.1
  • 3
    • 24944508600 scopus 로고    scopus 로고
    • Institut de Chimie des Substances Naturelles, Gifsur-Yvette, France. Unpublished observations, 1987
    • Marazano, C. Institut de Chimie des Substances Naturelles, Gifsur-Yvette, France. Unpublished observations, 1987.
    • Marazano, C.1
  • 15
    • 24944455037 scopus 로고    scopus 로고
    • note
    • All complex structures were resolved by intensive NMR spectroscopy studies including 1D and 2D NMR experiments (COSY 90, NOESY, HMQC, HMBC).
  • 16
    • 24944443335 scopus 로고    scopus 로고
    • note
    • For this purpose, the enantiomer (+)-25 was synthezised starting from S-(-)-1-phenylethylamine. Note that, due to a resolution process resulting from dimerization, the enantiomeric purity of adducts 25 and 26 was expected to be much higher than the enantiomeric purity of the starting dihydropyridine 24.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.