Herein, we described a highly regio- and enantioselective
Friedel–Crafts
alkylation of aniline derivatives with in situ generated ortho-quinone methides enabled by chiral phosphoric acid,
furnishing a wide range of enantioenriched triarylmethanes bearing
three similar benzene rings in high yields (up to 98%) with excellent
stereoselectivities (up to 98% ee). Furthermore, the large-scale reactions
and diversified transformations of product demonstrate the practicality
of the protocol. Density functional theory calculations elucidate
the origin of the enantioselectivity.
The live Lactobacillus acidophilus (La) alleviated colitis by ameliorating intestinal barrier and suppressing inflammation. SCFAs modulated and enriched by La promoted the mitophagy/NLRP3 inflammasome pathway, which helped to improve gut functions.
Lycorine-type alkaloids are privileged structures in the drug development due to its attractive biological activities. In this paper, the carbonyl on the C ring was proved to have played a...
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