| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5215299 | Tetrahedron | 2015 | 8 Pages |
Abstract
1,3-Dipolar cycloaddition of various nitrile oxides to substituted N-vinylpyrroles proceed with high efficiency and selectivity with the formation of single isomer of 5-pyrrolyl-substituted isoxazoline. The reaction of N-vinylpyrroles with cyclic azomethine imines occurs regioselectively affording 7-(pyrrol-1-yl)- substituted pyrazolo[1,2-a]pyrazolones as a mixture of two diastereomers.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
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