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Volumn 77, Issue 7, 2012, Pages 3373-3380

Atropisomers of hindered triarylisocyanurates: Structure, conformation, stereodynamics, and absolute configuration

Author keywords

[No Author keywords available]

Indexed keywords

ABSOLUTE CONFIGURATION; ARYL SUBSTITUENTS; ATROPISOMERS; DFT COMPUTATIONS; DIASTEREOISOMERS; ENANTIOSELECTIVE HPLC; INTERCONVERSIONS; LOW TEMPERATURES; NMR SPECTRUM; ROTATION BARRIERS; STEREODYNAMICS; VIBRATIONAL CIRCULAR DICHROISM SPECTRUM;

EID: 84859569071     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo300192n     Document Type: Article
Times cited : (14)

References (76)
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    • Misawa, H.; Koseki, T. Patent JP 03,166,255, 1991.
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    • Misawa, H.1    Koseki, T.2
  • 13
    • 84859570560 scopus 로고
    • Patent JP 0187,649
    • Nagai, H.; Komya, T. Patent JP 0187,649, 1989.
    • (1989)
    • Nagai, H.1    Komya, T.2
  • 31
    • 0003550821 scopus 로고    scopus 로고
    • The computed averaged interproton methyl distances are 4.08 Å in the case of the syn (meso) 2b and 6.43 Å in the case of the anti (racemic) 2a. As required when dealing with NOE experiments, these averages were obtained by taking into account the 6th root, according to Claridge, T. D. W. High Resolution NMR Techniques in Organic Chemistry; Pergamon: Oxford, UK, 1999; p 303. (If the 6th root is not applied, the corresponding averaged distances become 4.84 and 6.69 Å, respectively.)
    • (1999) High Resolution NMR Techniques in Organic Chemistry , pp. 303
    • Claridge, T.D.W.1
  • 66
    • 84857224047 scopus 로고    scopus 로고
    • Wavefunction Inc. Irvine, CA
    • Package TITAN 1.0.5; Wavefunction Inc.: Irvine, CA.
    • Package TITAN 1.0.5
  • 71
    • 84857224344 scopus 로고    scopus 로고
    • Gaussian Inc. Wallingford, CT
    • Package GaussView 5.0.9; Gaussian Inc.: Wallingford, CT, 2009.
    • (2009) Package GaussView 5.0.9


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.