| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5220154 | Tetrahedron | 2012 | 6 Pages |
Abstract
A highly diastereoselective and regioselective [2+2]-cycloaddition reaction of 3-ylideneoxindoles has been accomplished using visible light photocatalysis. This visible light photocatalytic protocol allows an expedient access to diversely functionalized and structurally constrained oxindole derivatives containing two spirocycles and four stereogenic centers, including two all-carbon quaternary centers.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
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