| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5276843 | Tetrahedron Letters | 2007 | 4 Pages |
Abstract
An efficient microwave-assisted, ZrOCl2·8H2O mediated, synthesis of novel dispiro-oxindolopyrrolidines and -pyrrolizidines was accomplished through [3+2] cycloaddition reaction of azomethine ylides derived from acenaphthenequinone and sarcosine/l-proline with (E)-2-oxoindolino-3-ylidene acetophenones in good yields.
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
A.R. Suresh Babu, R. Raghunathan,
![First Page Preview: ZrOCl2·8H2O mediated microwave induced [3+2] cycloaddition of azomethine ylides-a facile one-pot synthesis of novel dispiroheterocycles ZrOCl2·8H2O mediated microwave induced [3+2] cycloaddition of azomethine ylides-a facile one-pot synthesis of novel dispiroheterocycles](/preview/png/5276843.png)