Generating Skeletal Diversity and Complexity from Boron‐Substituted 1,3‐Dienes and Enophiles

Boron‐substituted 1,3‐dienes participate in ene reactions to afford new functionalized synthetic intermediates. After evaluating several enophiles as partners, the resulting products have been engaged in multistep sequences involving first a Diels Alder/allylboration process. A variety of skeletally...

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Veröffentlicht in:	European journal of organic chemistry 2020-06, Vol.2020 (22), p.3282-3293
Hauptverfasser:	François, Benjamin, Eberlin, Ludovic, Berrée, Fabienne, Whiting, Andrew, Carboni, Bertrand
Format:	Artikel
Sprache:	eng
Schlagworte:	Allylboration Boron Chemical Sciences Complexity Cycloaddition Dienes Diketones Lactones Organic chemistry Pericyclic reactions Spiro compounds Substitutes Synthetic methods
Online-Zugang:	Volltext
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