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Volumn 17, Issue 8, 2011, Pages 2365-2368

Asymmetric crossed-conjugate addition of nitroalkenes to enones by a chiral bifunctional diamine organocatalyst

Author keywords

asymmetric catalysis; crossed conjugate addition; enones; nitroalkenes; organocatalysis

Indexed keywords

ASYMMETRIC CATALYSIS; CROSSED-CONJUGATE ADDITION; ENONES; NITROALKENES; ORGANOCATALYSIS;

EID: 79951622959     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.201002961     Document Type: Article
Times cited : (19)

References (64)
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    • some selected examples on asymmetric synthesis of the nitro product
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    • note
    • 2 (10 mL) for 30 min at 25°C, then the solvent was evaporated to afford the corresponding DPEN salt, which was used directly as the catalyst in the reaction.
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    • Experimental details see the Supporting Information
    • For experimental details see the Supporting Information.
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    • note
    • The stereochemistry of the products was assigned based on the X-ray crystal structures of 3ga. CCDC-790928 (3ga) contains the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.