| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 7827248 | Tetrahedron | 2018 | 6 Pages |
Abstract
A Ni-catalyzed addition of arylboronic acids to isatins was first developed. The reaction, driven by Ni(acac)2 and dppp, gave 3-aryl-3-hydroxy-2-oxindoles in up to 97% yield. Substituted phenylboronic acids along with fused-ring and heterocyclic boronic acids reacted with isatins smoothly.147
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Authors
Yu-Yang Zhang, Huixuan Chen, Xiaoding Jiang, Hao Liang, Xuefeng He, Yaqi Zhang, Xiangmeng Chen, Wenhuan He, Yongsu Li, Liqin Qiu,