Abstract
The one-pot three-component reaction of p-quinone monoacetals (or p-quinol ethers), l-proline and naphthols is developed for the synthesis of N-aryl-2-arylpyrrolidines under mild conditions with high chemo-and regioselectivity. The reaction may involve multiple processes including condensation, decarboxylation and demethoxylation for the the generation of N-arylated 3,4-dihydro-2H-pyrrolium followed by controllable capture by naphthols. In the absence of a naphthol, p-quinone monoacetal coupled with l-proline to form a complex dipyrroloquinoline product.
Original language | English |
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Pages (from-to) | 297-303 |
Number of pages | 7 |
Journal | Organic Chemistry Frontiers |
Volume | 8 |
Issue number | 2 |
DOIs | |
State | Published - 21 Jan 2021 |