Michael Addition Initiated Carbocyclization Sequences with Nitroolefins for the Stereoselective Synthesis of Functionalized Heterocyclic and Carbocyclic Systems

The synthesis of various heterocycles and carbocycles (tetrahydrofurans, pyrrolidines, cyclopentanes) has been achieved by using new and efficient ionic addition/cyclization sequences. Nitroolefins play an important role in the Michael addition induced ring‐closing reactions (MIRC) reported in the p...

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Veröffentlicht in:	Chemistry : a European journal 2009-11, Vol.15 (45), p.12470-12488
Hauptverfasser:	Dumez, Estelle, Durand, Anne-Catherine, Guillaume, Martial, Roger, Pierre-Yves, Faure, Robert, Pons, Jean-Marc, Herbette, Gaëtan, Dulcère, Jean-Pierre, Bonne, Damien, Rodriguez, Jean
Format:	Artikel
Sprache:	eng
Schlagworte:	Alkenes - chemistry Chemical Sciences Cyclization cycloaddition Cyclopentanes - chemical synthesis Cyclopentanes - chemistry Cyclopropanes - chemical synthesis Cyclopropanes - chemistry domino reactions Furans - chemical synthesis Furans - chemistry Heterocyclic Compounds - chemical synthesis Heterocyclic Compounds - chemistry Michael addition Molecular Structure nitroolefins Organic chemistry Stereoisomerism
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