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Volumn 48, Issue 27, 2007, Pages 4749-4753

Cascade and one-pot processes providing substituted quinolines from aldimines and allylsilanes: auto-tandem catalysis of triflic imide

Author keywords

[No Author keywords available]

Indexed keywords

ALDIMINE DERIVATIVE; IMINE; QUINOLINE DERIVATIVE; SILANE DERIVATIVE; TRIFLUOROMETHANESULFONIC ACID; UNCLASSIFIED DRUG;

EID: 34249906469     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2007.05.032     Document Type: Article
Times cited : (38)

References (27)
  • 15
    • 0035898269 scopus 로고    scopus 로고
    • For a representative review on imino Diels-Alder reaction, see:
    • For a representative review on imino Diels-Alder reaction, see:. Buonora P., Olsen J.-C., and Oh T. Tetrahedron 57 (2001) 6099-6138
    • (2001) Tetrahedron , vol.57 , pp. 6099-6138
    • Buonora, P.1    Olsen, J.-C.2    Oh, T.3
  • 16
    • 34249884028 scopus 로고    scopus 로고
    • Desilylated quinoline 9, which would be transformed from 4ab, was also obtained in 6% yield.
  • 17
    • 9744257740 scopus 로고    scopus 로고
    • Definition of 'auto-tandem catalysis':
    • Definition of 'auto-tandem catalysis':. Fogg D.E., and dos Santos E.N. Coord. Chem. Rev. 248 (2004) 2365-2379
    • (2004) Coord. Chem. Rev. , vol.248 , pp. 2365-2379
    • Fogg, D.E.1    dos Santos, E.N.2
  • 19
    • 0344924960 scopus 로고    scopus 로고
    • Recent representative examples for auto-tandem catalysis, see:
    • Recent representative examples for auto-tandem catalysis, see:. Field L.D., Messerle B.A., and Wren S.L. Organometallics 22 (2003) 4393-4395
    • (2003) Organometallics , vol.22 , pp. 4393-4395
    • Field, L.D.1    Messerle, B.A.2    Wren, S.L.3
  • 25
    • 0000005220 scopus 로고
    • 3. However, the process constitutes hetero-Diels-Alder reaction, elimination of alcohol and dehydrogenation: see:
    • 3. However, the process constitutes hetero-Diels-Alder reaction, elimination of alcohol and dehydrogenation: see:. Kobayashi S., Ishitani H., and Nagayama S. Chem. Lett. (1995) 423-424
    • (1995) Chem. Lett. , pp. 423-424
    • Kobayashi, S.1    Ishitani, H.2    Nagayama, S.3
  • 26
    • 34249870915 scopus 로고    scopus 로고
    • note
    • 2NH, 84% yield of 4aa was obtained by DDQ-oxidation of 3aa under the similar conditions.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.