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Volumn 50, Issue 36, 2011, Pages 8416-8419

Intramolecular [2+2] photocycloaddition of substituted isoquinolones: Enantioselectivity and kinetic resolution induced by a chiral template

Author keywords

cycloaddition; enantioselectivity; hydrogen bonds; kinetic resolution; photochemistry

Indexed keywords

CHIRAL TEMPLATES; CYCLOBUTANES; HIGH ENANTIOSELECTIVITY; KINETIC RESOLUTION; PHOTOCYCLOADDITION; PHOTOPRODUCTS; RACEMIC SUBSTRATES;

EID: 80052100290     PISSN: 14337851     EISSN: 15213773     Source Type: Journal    
DOI: 10.1002/anie.201103051     Document Type: Article
Times cited : (49)

References (50)
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    • (Eds.: Y. Inoue, V. Ramamurthy), Marcel Dekker, New York
    • Y. Inoue, in Molecular and Supramolecular Photochemistry, Vol. 11 (Eds.:, Y. Inoue, V. Ramamurthy,), Marcel Dekker, New York, 2004, pp. 129-177.
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    • Inoue, Y.1
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  • 38
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    • It was previously shown that photoproducts that exhibit a significantly lower association to template 10 than the respective substrates are formed with high enantiomeric excess:, B. Grosch, C. N. Orlebar, E. Herdtweck, M. Kaneda, T. Wada, Y. Inoue, T. Bach, Chem. Eur. J. 2004, 10, 2179-2189.
    • (2004) Chem. Eur. J. , vol.10 , pp. 2179-2189
    • Grosch, B.1    Orlebar, C.N.2    Herdtweck, E.3    Kaneda, M.4    Wada, T.5    Inoue, Y.6    Bach, T.7


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.