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Volumn 21, Issue 16, 2015, Pages 6037-6041

Catalytic Asymmetric Addition of Meldrum's Acid, Malononitrile, and 1,3-Dicarbonyls to ortho-Quinone Methides Generated In Situ under Basic Conditions

Author keywords

asymmetric catalysis; enantioselectivity; organocatalysis; quinone methides; sulfones

Indexed keywords

CATALYSIS; CHEMICAL COMPOUNDS; ENANTIOSELECTIVITY; REACTION KINETICS;

EID: 84926313366     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.201500710     Document Type: Article
Times cited : (102)

References (78)
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    • note
    • As reported in ref. [19] there is usually no difference in reactivity between phenyl and p-tolyl sulfones. In ref. [22a] an example of tuning the leaving group ability of the sulfonyl group for imine formation from α-amido sulfones has been reported, however, using an electron-withdrawing group on the aryl ring of the sulfone.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.