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- Chiral 1,1-diaryl compounds as important pharmacophores. Dana Ameen, Timothy J. Snape
, Med. Chem. Commun.
, 2013
, 4
, 893
- Stereoselective synthesis of tri-substituted tetrahydrothiophenes and their in silico binding against mycobacterial protein tyrosine phosphatase B. Anshul Jain, Sushobhan Maji, Khyati Shukla, Akanksha Kumari, Shivani Garg, Ramesh K. Metre, Sudipta Bhattacharyya, Nirmal K. Rana
, Org. Biomol. Chem.
, 2022
, 20
, 3124
- Standardised thin-layer chromatographic systems for the identification of drugs and poisons. A review. A. H. Stead, R. Gill, T. Wright, J. P. Gibbs, A. C. Moffat
, Analyst
, 1982
, 107
, 1106
- Ultrasonic relaxations associated with aggregation in drugs. Derek Causon, John Gettins, John Gormally, Richard Greenwood, Najagopalan Natarajan, Evan Wyn-Jones
, J. Chem. Soc., Faraday Trans. 2
, 1981
, 77
, 143
- Oxidation procedures in the assay of some drugs containing a diphenylmethylene ether or diphenylmethyleneamino group. B. Caddy, F. Fish, J. Tranter
, Analyst
, 1974
, 99
, 555
- Chiral separation of five antihistamine drug enantiomers and enantioselective pharmacokinetic study of carbinoxamine in rat plasma by HPLC-MS/MS. Meng Li, Junyuan Zhang, Siman Ma, Zhen Jiang, Xin Di, Xingjie Guo
, New J. Chem.
, 2020
, 44
, 5819
- Computational design of syntheses leading to compound libraries or isotopically labelled targets. Karol Molga, Piotr Dittwald, Bartosz A. Grzybowski
, Chem. Sci.
, 2019
, 10
, 9219
- B(C6F5)3-catalyzed tandem protonation/deuteration and reduction of in situ-formed enamines. Rongpei Wu, Ke Gao
, Org. Biomol. Chem.
, 2021
, 19
, 4032
- Applications of sulfuryl fluoride (SO2F2) in chemical transformations. Ravindar Lekkala, Revathi Lekkala, Balakrishna Moku, K. P. Rakesh, Hua-Li Qin
, Org. Chem. Front.
, 2019
, 6
, 3490
- Hybrid molecules based on an emodin scaffold. Synthesis and activity against SARS-CoV-2 and Plasmodium. Youzhi Li, Franck Touret, Xavier de Lamballerie, Michel Nguyen, Marion Laurent, Françoise Benoit-Vical, Anne Robert, Yan Liu, Bernard Meunier
, Org. Biomol. Chem.
, 2023
, 21
, 7382