| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5269249 | Tetrahedron Letters | 2014 | 4 Pages |
Abstract
An efficient one-step method has been developed to construct furans via a Suzuki-Miyaura cross-coupling reaction of 1,2-oxaborol-2(5H)-ols with carboxylic anhydrides. In the presence of Pd(OAc)2/PCy3, the multi-substituted alkenylboron compounds could couple with anhydrides to obtain furans in moderate-to-good yields. The addition of bases promoted the coupling reaction, and the plausible reaction mechanism was proposed.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Tao Yu, Xin-Yan Wu, Jun Yang,