Conjugated enones are one of the most used building blocks in synthetic organic chemistry[1] and are an important moiety in natural products and biologically active com- pounds. Given its high synthetic versatility, the enone system is involved in several carbon–carbon bond-forming reactions, such as cyclopropanation, Michael addition, Diels–Alder and 1,3-dipolar cycloaddition reactions, and in the conversion to other functional groups, such as allylic al- cohols, epoxides and amines.

One-Pot Consecutive Reactions Based on the Synthesis of Conjugated Enones by the Re-Catalysed Meyer-Schuster Rearrangement

PORTA, ALESSIO;ZANONI, GIUSEPPE;VIDARI, GIOVANNI
2012-01-01

Abstract

Conjugated enones are one of the most used building blocks in synthetic organic chemistry[1] and are an important moiety in natural products and biologically active com- pounds. Given its high synthetic versatility, the enone system is involved in several carbon–carbon bond-forming reactions, such as cyclopropanation, Michael addition, Diels–Alder and 1,3-dipolar cycloaddition reactions, and in the conversion to other functional groups, such as allylic al- cohols, epoxides and amines.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11571/717621
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