对映选择合成
化学
合成大麻素
部分
有机催化
组合化学
立体化学
有机化学
催化作用
生物化学
大麻素
受体
作者
Andreu Vidal‐Albalat,Bruno Matos Paz
标识
DOI:10.1002/adsc.202301168
摘要
Abstract Flavonoids and cannabinoids comprise two large families of natural products that contain a chromane moiety in their structure. Their therapeutic potential has been extensively investigated as potential treatments to several diseases, ranging from cancer to infectious and neurodegenerative diseases. Despite their relative structural simplicity, in recent years creative synthetic methodologies were designed to overcome limitations from the previous synthetic strategies applied to these compounds. The aim of this review is to provide a comprehensive overview of all the enantioselective organocatalytic strategies that have been applied to the synthesis of flavonoids and cannabinoids to date.
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