Abstract
The value of functional pyrrolidines in the fields of biology, pharmacology, catalysis, and natural product synthesis stimulates an intensive interest in developing new synthetic methods for this class of compounds, and direct functionalization of the simple pyrrolidine represents an attractive and effective approach. Herein, a metal-free protocol for direct N-arylationand -functionalization of pyrrolidine via redox-neutral three-component reactions is reported, in which p-quinolethers or p-quinone monoacetals serve as the arylation components and the formal oxidants for -functionalization of pyrrolidine.
Original language | English |
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Pages (from-to) | 2574-2584 |
Number of pages | 11 |
Journal | Synthesis (Germany) |
Volume | 54 |
Issue number | 11 |
DOIs | |
State | Published - 8 Mar 2022 |
Keywords
- N -arylation
- phosphinylation
- pyrrolidine
- redox-neutral MCR
- α-functionalization