Solid-Phase Synthesis of Biaryls via the Stille Reaction
โ Scribed by Forman, Frank W.; Sucholeiki, Irving
- Book ID
- 111880278
- Publisher
- American Chemical Society
- Year
- 1995
- Tongue
- English
- Weight
- 678 KB
- Volume
- 60
- Category
- Article
- ISSN
- 0022-3263
No coin nor oath required. For personal study only.
๐ SIMILAR VOLUMES
AIbslBlmL-2-Amidophenol attached to a solid support can be converted to the corresponding benzoxazole by treatment with tdphenylphosphine and diathyl azodicarboxylate in THF at room temperature in high yield and purity. ยฉ 1997 l~lsevk~ ~ยข~mcยข Lt(L The synthesis and screening of small molecule combin
The synthesis of cis-azetidinones on solid support via the Staudinger reaction is described. The final products are obtained in high purity with no purification required.
A three-component Stille coupling reaction on solid phase is described. Diaryl ketones bearing a wide variety of functional groups were prepared with polymer-bound organostannane and aryl halides in the presence of carbon monoxide.