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Volumn 23, Issue 24, 2012, Pages 1657-1662

Catalytic enantioselective synthesis of atropisomeric 2-aryl-4-quinolinone derivatives with an N-C chiral axis

Author keywords

[No Author keywords available]

Indexed keywords

2 BROMOPHENYL ARYLETHYNYL KETONE; ANILINE DERIVATIVE; KETONE DERIVATIVE; QUINOLINE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 84870725965     PISSN: 09574166     EISSN: 1362511X     Source Type: Journal    
DOI: 10.1016/j.tetasy.2012.11.004     Document Type: Article
Times cited : (44)

References (60)
  • 1
    • 0000418012 scopus 로고
    • Typical examples of atropisomeric compounds with an N-C chiral axis
    • Typical examples of atropisomeric compounds with an N-C chiral axis: L.H. Bock, and R. Adams J. Am. Chem. Soc. 53 1931 374
    • (1931) J. Am. Chem. Soc. , vol.53 , pp. 374
    • Bock, L.H.1    Adams, R.2
  • 15
    • 3843110770 scopus 로고    scopus 로고
    • Tetrahedron symposium-in-print on axially chiral amides (atropisomerism)
    • Tetrahedron symposium-in-print on axially chiral amides (atropisomerism): J. Clayden Tetrahedron 60 2004 4325 4558
    • (2004) Tetrahedron , vol.60 , pp. 4325-4558
    • Clayden, J.1
  • 45
    • 84864059247 scopus 로고    scopus 로고
    • Recently we found that the rotational barrier of N-(ortho-tert- butylphenyl)-2-quinolinone is higher than 10 kcal/mol in comparison to that of N-(ortho-tert-butylphenyl)-3,4-dihydro-2-quinolinone. The high rotational barrier of N-(ortho-tert-butylphenyl)-2-quinolinone was disclosed to be due to the rigid aromatic structure
    • Recently we found that the rotational barrier of N-(ortho-tert- butylphenyl)-2-quinolinone is higher than 10 kcal/mol in comparison to that of N-(ortho-tert-butylphenyl)-3,4-dihydro-2-quinolinone. The high rotational barrier of N-(ortho-tert-butylphenyl)-2-quinolinone was disclosed to be due to the rigid aromatic structure: N. Suzumura, M. Kageyama, D. Kamimura, T. Inagaki, Y. Dobashi, H. Hasegawa, H. Fukaya, and O. Kitagawa Tetrahedron Lett. 53 2012 4332
    • (2012) Tetrahedron Lett. , vol.53 , pp. 4332
    • Suzumura, N.1    Kageyama, M.2    Kamimura, D.3    Inagaki, T.4    Dobashi, Y.5    Hasegawa, H.6    Fukaya, H.7    Kitagawa, O.8
  • 48
    • 0021076049 scopus 로고
    • Typical examples of SED through achiral chromatography
    • Typical examples of SED through achiral chromatography: K.C. Cundy, and P.A. Crooks J. Chromatogr. 281 1983 17
    • (1983) J. Chromatogr. , vol.281 , pp. 17
    • Cundy, K.C.1    Crooks, P.A.2
  • 60
    • 84870715024 scopus 로고    scopus 로고
    • CCDC-901836 4g contains the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via
    • CCDC-901836 4g contains the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via http://www.ccdc.com.ac.uk/data-request/cif.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.