| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1345145 | Tetrahedron: Asymmetry | 2014 | 5 Pages |
Abstract
The kinetic resolution of racemic C1-substituted oxabenzonorbornadienes was realized by iridium-catalyzed asymmetric [2+2] cycloaddition reaction with arylacetylenes. Cyclobutene products and unreacted C1-substituted oxabenzonorbornadienes were obtained with high to excellent enantiomeric purities.
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Related Topics
Physical Sciences and Engineering
Chemistry
Inorganic Chemistry
![Kinetic resolution of C1-substituted oxabenzonorbornadienes by Ir-catalyzed asymmetric [2+2] cycloaddition reactions with arylacetylenes](/preview/png/1345145.png "First Page Preview: Kinetic resolution of C1-substituted oxabenzonorbornadienes by Ir-catalyzed asymmetric [2+2] cycloaddition reactions with arylacetylenes")
Authors
Qingjing Yang, Lu Yu, Jianbin Xu, Sifeng Li, Shanshan Liu, Hualei Chen, Yongyun Zhou, Lin Wang, Baomin Fan,