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Volumn 10, Issue 11, 2012, Pages 2326-2338
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Asymmetric synthesis of α,β-diamino acid derivatives with an aziridine-, azetidine- and γ-lactone-skeleton via Mannich-type additions across α-chloro-N-sulfinylimines
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Author keywords
[No Author keywords available]
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Indexed keywords
ACID DERIVATIVE;
AMINO ESTERS;
ASYMMETRIC SYNTHESIS;
AZETIDINES;
AZIRIDINES;
BUILDING BLOCKES;
BUTYROLACTONES;
DIAMINO ACIDS;
DIASTEREOSELECTIVE;
ENOLATES;
MANNICH-TYPE REACTIONS;
RING CLOSURES;
RING TRANSFORMATION;
AMINO ACIDS;
CARBOXYLIC ACIDS;
ESTERIFICATION;
ESTERS;
STEREOSELECTIVITY;
IONIC LIQUIDS;
AMINO ACID;
AZETIDINE;
AZETIDINE DERIVATIVE;
AZIRIDINE;
AZIRIDINE DERIVATIVE;
CHLORINE DERIVATIVE;
IMINE;
LACTONE;
SULFUR DERIVATIVE;
ARTICLE;
CHEMICAL STRUCTURE;
CHEMISTRY;
STEREOISOMERISM;
AMINO ACIDS;
AZETIDINES;
AZIRIDINES;
CHLORINE COMPOUNDS;
IMINES;
LACTONES;
MODELS, MOLECULAR;
MOLECULAR STRUCTURE;
STEREOISOMERISM;
SULFUR COMPOUNDS;
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EID: 84857588948
PISSN: 14770520
EISSN: None
Source Type: Journal
DOI: 10.1039/c2ob06637h Document Type: Article |
Times cited : (35)
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References (63)
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