Abstract
The copper-catalyzed reaction of 5-substituted penta-1,4-diyn-3-yl acetates with P(O)H compounds to efficiently give a new class of phosphonyl diynes is reported. The reaction may take place through a regioselective nucleophilic attack of phosphorus nucleophiles on Cu-allenylidene intermediates to form allenyl intermediates followed by a rapid allene-alkyne isomerization process. The synthetic utility of the obtained products is demonstrated. (Figure presented.).
Original language | English |
---|---|
Pages (from-to) | 3897-3906 |
Number of pages | 10 |
Journal | Advanced Synthesis and Catalysis |
Volume | 358 |
Issue number | 23 |
DOIs | |
State | Published - 7 Dec 2016 |
Keywords
- C−P bond formation
- allenes
- copper catalysis
- diynes
- organophosphorus compounds