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RESEARCH PRODUCT
Dihydrooxazine Oxides as Key Intermediates in Organocatalytic Michael Additions of Aldehydes to Nitroalkenes
Gokarneswar SahooPetri M. PihkoMikko MelartoHasibur RahamanImre PápaiArto ValkonenÁDám Madarászsubject
chemistry.chemical_classificationchemistryOrganic chemistryProtonationGeneral ChemistryNuclear magnetic resonance spectroscopyGeneral Medicineta116CatalysisAlkyldescription
Pause and play: dihydrooxazine oxides are stable intermediates that are protonated directly, without the intermediacy of the zwitterions, in organocatalytic Michael additions of aldehydes and nitroalkenes (see scheme, R=alkyl). Protonation of these species explains both the role of the acid co-catalyst in these reactions, and the observed stereochemistry when the reaction is conducted with α-alkylnitroalkenes.
year | journal | country | edition | language |
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2012-11-13 | Angewandte Chemie |