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Volumn 17, Issue 8, 2011, Pages 2358-2360

Direct asymmetric Michael addition of cyclic N-sulfonylimines to α,β-unsaturated aldehydes

Author keywords

aldehydes; aminocatalysis; Michael addition; piperidines; sulfonylimines

Indexed keywords

ACETOPHENONES; ACTIVATED IMINES; AMINE COMPOUNDS; AMINOCATALYSIS; CATALYTIC CONDITIONS; ELECTRON-WITHDRAWING SUBSTITUENTS; ELECTRONWITHDRAWING; ELECTROPHILES; ENAMIDES; FUNCTIONALIZATION REACTIONS; MANNICH REACTIONS; MANNICH-TYPE REACTIONS; MICHAEL ADDITIONS; NITROGEN ATOM; ORGANIC MOLECULES; PIPERIDINES; SULFONYLIMINES; TAUTOMERIZATIONS; UNSATURATED ALDEHYDES;

EID: 79951649294     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.201002592     Document Type: Article
Times cited : (37)

References (43)
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    • Cyclic imines with alkylsulfonyl structures of the type reported in ref. [6c] did not react
    • Cyclic imines with alkylsulfonyl structures of the type reported in ref. [6c] did not react.
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    • CCDC-799810 (9) contains the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via
    • CCDC-799810 (9) 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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    • For a plausible reaction mechanism, see the Supporting Information
    • For a plausible reaction mechanism, see the Supporting Information.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.