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Rhodium-catalyzed asymmetric 1,4-addition of arylboron compounds generated in situ from aryl bromides

✍ 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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✦ 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.


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Chiral Heterodisulfoxide Ligands in Rhod
✍ Fuzhong Han; Guihua Chen; Xiangyang Zhang; Jian Liao πŸ“‚ Article πŸ“… 2011 πŸ› John Wiley and Sons 🌐 English βš– 379 KB πŸ‘ 1 views

## Abstract A new family of benzene‐based chiral heterodisulfoxide ligands **L1**–**L5** was synthesized in a single step. These disulfoxide ligands were applied in the rhodium‐catalyzed asymmetric 1,4‐addition of arylboronic acids to chromenones. The addition of diverse arylboronic acids to chrome