Tejender S. Thakur, Ph.D.
Affiliations: | 2011- | Molecular and Structural Biology | CSIR-Central Drug Research Institute |
Area:
Crystal Engineering, Computational Chemistry, X-ray CrystallographyGoogle:
"Tejender S. Thakur"Mean distance: (not calculated yet)
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Publications
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| Dash SG, Thakur TS. (2019) Cationcation hydrogen bonds in synephrine salts: a typical interaction in an unusual environment. Physical Chemistry Chemical Physics : Pccp. 21: 20647-20660 |
| Dash SG, Singh SS, Thakur TS. (2019) Structural Landscape-Guided Exploration of a New Polymorph of 4-Nitrobenzoic Acid Crystal Growth & Design. 19: 952-958 |
| Rajbongshi T, Sarmah KK, Sarkar A, et al. (2018) Preparation of Pyrazinamide Eutectics versus Cocrystals Based on Supramolecular Synthon Variations Crystal Growth & Design. 18: 6640-6651 |
| Mehta BK, Singh SS, Chaturvedi S, et al. (2018) Rational Coformer Selection and the Development of New Crystalline Multicomponent Forms of Resveratrol with Enhanced Water Solubility Crystal Growth & Design. 18: 1581-1592 |
| Singh SS, Vasantha KY, Sattur AP, et al. (2016) Experimental and computational crystal structure landscape study of nigerloxin: a fungal metabolite from Aspergillus niger Crystengcomm. 18: 1740-1751 |
| Thakur TS, Dubey R, Desiraju GR. (2015) Intermolecular atom-atom bonds in crystals - a chemical perspective. Iucrj. 2: 159-60 |
| Thakur TS, Dubey R, Desiraju GR. (2015) Crystal structure and prediction. Annual Review of Physical Chemistry. 66: 21-42 |
| Thakur TS, Singh SS. (2015) Studying the Role of C═O···C═O, C═O···N–O, and N–O···N–O Dipole–Dipole Interactions in the Crystal Packing of 4-Nitrobenzoic Acid and 3,3′-Dinitrobenzophenone Polymorphs: An Experimental Charge Density Study Crystal Growth & Design. 15: 3280-3292 |
| Singh SS, Thakur TS. (2014) New crystalline salt forms of levofloxacin: conformational analysis and attempts towards the crystal structure prediction of the anhydrous form Crystengcomm. 16: 4215 |
| Shigemitsu H, Hisaki I, Kometani E, et al. (2013) Crystalline supramolecular nanofibers based on dehydrobenzoannulene derivatives. Chemistry (Weinheim An Der Bergstrasse, Germany). 19: 15366-77 |