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Volumn 54, Issue 21, 2015, Pages 6320-6324

Organocatalytic asymmetric addition of naphthols and electron-rich phenols to isatin-derived ketimines: Highly enantioselective construction of tetrasubstituted stereocenters

Author keywords

asymmetric synthesis; Friedel Crafts reactions; isatin derived ketimines; naphthols; organocatalysis

Indexed keywords

FRIEDEL-CRAFTS REACTION; NAPHTHOL; PHENOLS; REACTION KINETICS; SYNTHESIS (CHEMICAL);

EID: 85027929604     PISSN: 14337851     EISSN: 15213773     Source Type: Journal    
DOI: 10.1002/anie.201501273     Document Type: Article
Times cited : (126)

References (121)
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    • For seminal studies on the use of catalyst III for the addition of nucleophiles to imines, see
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    • The N1-unprotected isatin showed lower reactivity, and the corresponding product was obtained in moderate yield (56%) with a low eevalue (11%).
    • The N1-unprotected isatin showed lower reactivity, and the corresponding product was obtained in moderate yield (56%) with a low eevalue (11%).
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    • See the Supporting Information for further details. CCDC1048104 (3p) and 1048103 (5i) contain the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via.
    • See the Supporting Information for further details. CCDC1048104 (3p) and 1048103 (5i) contain the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/data-request/cif.
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    • [5c] in that case the product was formed with moderate enantioselectivity (63%ee).
    • [5c] in that case the product was formed with moderate enantioselectivity (63%ee).
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    • One example of the addition of 4a to 2a is described in Ref.[9c]; however, the eevalue of the product is low (43%).
    • One example of the addition of 4a to 2a is described in Ref.[9c]; however, the eevalue of the product is low (43%).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.