The syntheses of functionalized 2-alkenyl and alkynyl-1-β-methyl-carbapenems via the stille cross-coupling reaction
✍ Scribed by Kevin D. Dykstra; Frank DiNinno
- Book ID
- 108386584
- Publisher
- Elsevier Science
- Year
- 1998
- Tongue
- French
- Weight
- 224 KB
- Volume
- 39
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
## Abstract A systematic study on the __Stille__ and __Sonogashira__ cross‐coupling of iodinated imidazo[1,2‐__a__]pyridines was performed, permitting the preparation of various vinyl‐, ethynyl‐, and allenyl‐substituted derivatives. These methods are particularly valuable, given their experimental
## Abstract 1‐(2′‐deoxy‐2′‐fluoro‐__β__‐D‐arabinofuranosyl)‐[__methyl__‐^11^C]thymine ([^11^C]FMAU) [^11^C]‐**1** was synthesised __via__ a palladium‐mediated Stille coupling reaction of 1‐(2′‐deoxy‐2′‐fluoro‐__β__‐D‐arabinofuranosyl)‐5‐(trimethylstannyl)uracil **2** with [^11^C]methyl iodide in a