A novel, thioacetal based linker for solid-phase synthesis
✍ Scribed by Christoph M Huwe; Hermann Künzer
- Publisher
- Elsevier Science
- Year
- 1999
- Tongue
- French
- Weight
- 286 KB
- Volume
- 40
- Category
- Article
- ISSN
- 0040-4039
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✦ Synopsis
Commercially available (+)-ct-lipoic acid was employed as a novel, chemically robust linker for the immobilization of ketones. The utility of this thioacetal based linker in solid-phase synthesis was demonstrated by synthesizing several 4-acetylbiphenyls and 4-alkoxyacetophenones via Suzuki and Mitsunobu reactions, respectively. The products were easily cleaved from solid support by treatment with [bis(trifluoroacetoxy)iodo]benzene.
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