| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5233879 | Tetrahedron | 2005 | 12 Pages |
Abstract
A number of potent pyrimido[4,5-d]pyrimidine analogues have been efficiently synthesized by hetero Diels-Alder cycloaddition. The molecular mechanism of the observed cycloaddition reaction has been investigated by means of theoretical studies at semiempirical PM3 level.
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Pratibha Sharma, Ashok Kumar, Nilesh Rane, Vamsi Gurram,
![First Page Preview: Hetero Diels-Alder reaction: a novel strategy to regioselective synthesis of pyrimido[4,5-d]pyrimidine analogues from Biginelli derivative Hetero Diels-Alder reaction: a novel strategy to regioselective synthesis of pyrimido[4,5-d]pyrimidine analogues from Biginelli derivative](/preview/png/5233879.png)