| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1411926 | Journal of Molecular Structure | 2007 | 7 Pages |
Abstract
X-ray crystallographic analysis of two new ‘Leonard/trimethylene linker’ compounds; 1,3-bis(4-methoxy-6-methylsulfonyl-lH-pyrazolo[3,4-d]pyrimidin-1-yl)propane (4a) and 1,3-bis(4-ethoxy-6-methylsulfonyl-lH-pyrazolo[3,4-d]pyrimidin-1-yl)propane (4b) not only confirm robustness of the unusual U-motif conformation seen in earlier related compounds (1 and 2) but in addition reveal novel chain motif formed due to intermolecular CH⋯O and CH⋯N interactions resulting in novel plus (+) motif.
Keywords
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Kamlakar Avasthi, Sheikh M. Farooq, Sangeeta Aswal, Resmi Raghunandan, Prakas R. Maulik,
![First Page Preview: 1H NMR and crystallographic evidence for tolerance of bulky electron withdrawing methanesulfonyl group on robustness of the U-motif in pyrazolo[3,4-d]pyrimidine core based ‘Leonard linker’ compounds and formation of plus (+) motif 1H NMR and crystallographic evidence for tolerance of bulky electron withdrawing methanesulfonyl group on robustness of the U-motif in pyrazolo[3,4-d]pyrimidine core based ‘Leonard linker’ compounds and formation of plus (+) motif](/preview/png/1411926.png)