Abstract
The mechanism of thermal decomposition of nine acetylenic esters has been examined under conditions of flash vacuum pyrolysis. The products formed may be explained by a series of well-precedented steps involving such processes as ene reactions, alkyne to vinylidene rearrangements, carbene CH insertions, and fragmentation of 2,3-dihydrofuran-2-ones or 5,6-dihydropyran-2-ones with extrusion of CO and CO2 respectively.
Original language | English |
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Pages (from-to) | 103-112 |
Number of pages | 10 |
Journal | ARKIVOC |
Volume | 9 |
Issue number | x |
Publication status | Published - 2008 |
Keywords
- Acetylenic ester
- alkyne
- carbene
- fragmentation
- pyrolysis
- STABILIZED PHOSPHORUS YLIDES
- FLASH VACUUM PYROLYSIS
- TERMINAL ALKYNES
- GENERATION
- PROPIOLATE