Rhodium-catalyzed asymmetric 1,4-addition of arylboron compounds generated in situ from aryl bromides
β Scribed by Yoshiaki Takaya; Masamichi Ogasawara; Tamio Hayashi
- Book ID
- 104262194
- Publisher
- Elsevier Science
- Year
- 1999
- Tongue
- French
- Weight
- 265 KB
- Volume
- 40
- Category
- Article
- ISSN
- 0040-4039
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β¦ Synopsis
Rhodium-catalyzed asymmetric 1,4-addition to 0t,13-unsaturated ketones is effected by use of arylborates, generated in situ by lithiation of aryl bromides followed by treatment with trimethoxyborane, to give the corresponding [3-aryl ketones of up to 99% ee in high yields. The addition of I equiv. (to arylborate) of water is essential for high chemical yields.
π SIMILAR VOLUMES
## Abstract A new family of benzeneβbased chiral heterodisulfoxide ligands **L1**β**L5** was synthesized in a single step. These disulfoxide ligands were applied in the rhodiumβcatalyzed asymmetric 1,4βaddition of arylboronic acids to chromenones. The addition of diverse arylboronic acids to chrome
## Abstract For Abstract see ChemInform Abstract in Full Text.