Asymmetric pyrone Diels–Alder reactions enabled by dienamine catalysis?

Chemical Science Pub Date: 2019-12-26 DOI: 10.1039/C9SC05738B

Abstract

Despite the proven value in utilizing pyrone dienes to create molecular complexity via Diels–Alder reactions with varied dienophiles, few examples of effective catalytic, asymmetric variants of this process have been developed. Herein, we show that the use of J?rgensen–Hayashi-type catalysts can convert an array of α,β-unsaturated aldehydes into chiral dienamines that can formally add in a Diels–Alder fashion to a number of electron-deficient pyrones of the coumalate-type to generate optically active [2.2.2]-bicyclic lactones. In most cases, the reactions proceed with good to excellent diastereo- and enantiocontrol (up to 99% ee). Models to explain that stereoselectivity, as well as several additional transformations of the resultant products, are also presented.

Graphical abstract: Asymmetric pyrone Diels–Alder reactions enabled by dienamine catalysis
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