| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5276995 | Tetrahedron Letters | 2010 | 4 Pages |
Abstract
A new efficient route for the synthesis of substituted 2H-pyrrolopyrimidines (9-deazaxanthine analogs) via thiophenol mediated radical cyclization has been achieved. The stereochemistry of the newly synthesised compounds has been settled from NOE data.
Graphical abstractDownload full-size image
Keywords
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
![Thiophenol mediated radical cyclization: an expedient approach to 2H-pyrrolo[3,2-d]pyrimidines (9-deazaxanthine analogs)](/preview/png/5276995.png "First Page Preview: Thiophenol mediated radical cyclization: an expedient approach to 2H-pyrrolo[3,2-d]pyrimidines (9-deazaxanthine analogs)")
Authors
K.C. Majumdar, Shovan Mondal, Debankan Ghosh,