| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5270282 | Tetrahedron Letters | 2014 | 6 Pages |
Abstract
The synthesis of [a]-annelated pyrazolopyrroloindoles via intramolecular 1,3-dipolar cycloaddition of in situ generated azomethine imine from N-allylated indole-2-carboxaldehyde, in regio- and stereoselective manner by using microwave irradiation is described. A one-pot strategy for the expedient synthesis of pyrazolopyrroloindoles has been developed.
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
![Microwave-assisted facile synthesis of [a]-annelated pyrazolopyrroloindoles via intramolecular azomethine imine 1,3-dipolar cycloaddition](/preview/png/5270282.png "First Page Preview: Microwave-assisted facile synthesis of [a]-annelated pyrazolopyrroloindoles via intramolecular azomethine imine 1,3-dipolar cycloaddition")
Authors
Anand H. Shinde, Shinde Vidyacharan, Duddu S. Sharada,