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Volumn 69, Issue 25, 2004, Pages 8739-8744

Mild and selective reduction of imines: Formation of an unsymmetrical macrocycle

Author keywords

[No Author keywords available]

Indexed keywords

DEUTERIUM; REACTION KINETICS; REDUCTION;

EID: 10044232993     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo049197u     Document Type: Article
Times cited : (53)

References (65)
  • 52
    • 10044240102 scopus 로고    scopus 로고
    • note
    • It was impossible to identify exactly which imine was reduced because of disorder. The macrocycle appears to pack equally well with the imine or amine in any position, as there is a crystallographic mirror plane through the middle of the macrocycle (i.e., it appears more symmetrical as a result of disorder).
  • 55
    • 10044295736 scopus 로고    scopus 로고
    • note
    • 1H NMR spectroscopy and MS).
  • 56
    • 10044249606 scopus 로고    scopus 로고
    • note
    • Because of the difficulty of purifying 7 with short alkoxy chains, 7 with tetradecyloxy chains was used for these experiments.
  • 62
    • 0000513097 scopus 로고    scopus 로고
    • + coordinate to imines to generate electrophilic iminium ions that react with nucleophiles. For example, see: Mayer, M. F.; Hossain, M. M. J. Org. Chem. 1998. 63, 6839-6844.
    • (1998) J. Org. Chem. , vol.63 , pp. 6839-6844
    • Mayer, M.F.1    Hossain, M.M.2
  • 65
    • 10044285010 scopus 로고    scopus 로고
    • note
    • - (X = H, Na, K, Rb, Cs).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.