The Preparation of Hindered Biphenyls via the Suzuki Reaction. -The method allows the preparation of type (IV) in "good yield" with exception of (IVd). The products may be of interest for the synthesis of balanol analogues (structure-activity studies).
The preparation of hindered biphenyls via the suzuki reaction
β Scribed by Mary George Johnson; Robert J. Foglesong
- Publisher
- Elsevier Science
- Year
- 1997
- Tongue
- French
- Weight
- 89 KB
- Volume
- 38
- Category
- Article
- ISSN
- 0040-4039
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β¦ Synopsis
The preparation of a number of hindered biphenyls is presented in which the mylboronate suffers from both steric crowding and eleamn wit_Mmwing group deactivation.
π SIMILAR VOLUMES
Treatment of a vinyl resin with 9-BBN affords a polymer bound alkylborane that undergoes palladium-catalyzed Suzuki cross coupling reactions with a variety of aromatic, vinylic and aliphatic halides. The mild reaction conditions are compatible with several functional groups and allow carbon-carbon b
## Abstract magnified image A facile and convenient method for the synthesis of highly functionalized 2β(substitutedbiphenyl) based benzimidazoles has been reported by the application of SuzukiβMiyaura cross coupling reaction.