Unusual effect of bulky isopropyl group on robustness of the U-motif in pyrazolo[3,4-d]pyrimidine core based ‘Leonard linker’ compounds in comparison to methyl/ethyl group: A1H NMR and X-ray crystallographic study
Author:
Publisher
Elsevier BV
Subject
Inorganic Chemistry,Organic Chemistry,Spectroscopy,Analytical Chemistry
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Cited by 7 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Role of arene interactions and substituent effects in conformational (syn/anti) control of 1,2-diarylethanes;CrystEngComm;2012
2. Gas-phase conformational and intramolecular π–π interaction studies on some pyrazolo[3,4-d]pyrimidine derivatives;Computational and Theoretical Chemistry;2011-12
3. An alternative to ‘propylene/Leonard linker’ for studying arene interactions in flexible pyrazolo[3,4-d]pyrimidine core based models both at molecular and supramolecular levels;CrystEngComm;2011
4. Pyrazolo[3,4-d]pyrimidinophanes: Convenient Synthesis of a New Class of Cyclophane and X-ray Structure of the First Representative;Organic Letters;2009-10-29
5. Studies on arene interactions in flexible pyrazolo[3,4-d]pyrimidine core based symmetrical ‘propylene/Leonard linker’ models: X-ray crystallographic evidence for disappearance of intramolecular stacking due to presence of chloro- or cyano-groups in place of methylsulfanyl or alkoxy substituents;Journal of Molecular Structure;2009-06
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