SYNTHESIS OF ENANTIOMERICALLY ENRICHED 4-ARYL-3,4-DIHYDROCOUMARINS
DOI:
https://doi.org/10.1007/3148Keywords:
boronic acids, dihydrocoumarins, 1, 4-addition, enantioselective synthesisAbstract
Several synthetic approaches are known for the preparation of chiral 4-aryl-3,4-dihydrocoumarins (DHCs). This article considers recently discovered methods for the synthesis of chiral DHCs: enantioselective Rh(I)-catalyzed 1,4-addition of arylboronic acids to α,β-unsaturated carbonyl compounds, asymmetric reduction of coumarins, oxidation of chiral indanones, hydroesterification of alkenylphenols, and the addition of 1,3-dicarbonyl compounds to o-quinone methides.
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Published
2016-08-11
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Section
Heterocycles in Focus