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- Palladium-catalyzed allylic amination: a powerful tool for the enantioselective synthesis of acyclic nucleoside phosphonates. Mariam Azzouz, Sébastien Soriano, Margarita Escudero-Casao, M. Isabel Matheu, Sergio Castillón, Yolanda Díaz
, Org. Biomol. Chem.
, 2017
, 15
, 7227
- Modification of hygroscopicity and tabletability of l-carnitine by a cocrystallization technique. Zunting Pang, Xingye Weng, Yuanfeng Wei, Yuan Gao, Jianjun Zhang, Shuai Qian
, CrystEngComm
, 2021
, 23
, 2138
- Synthesis and antiviral activities of fluorinated acyclic nucleoside phosphonates. Wei Chen, Michael T. Flavin, Robert Filler, Ze-Qi Xu
, J. Chem. Soc., Perkin Trans. 1
, 1998
, 3979
- Saccharin salts of biologically active hydrazone derivatives. Artem O. Surov, Alexander P. Voronin, Anna A. Simagina, Andrei V. Churakov, Sophia Y. Skachilova, German L. Perlovich
, New J. Chem.
, 2015
, 39
, 8614
- Metal ion complexes of antivirally active nucleotide analogues. Conclusions regarding their biological action. Helmut Sigel
, Chem. Soc. Rev.
, 2004
, 33
, 191
- Prodrugs of pyrophosphates and bisphosphonates: disguising phosphorus oxyanions. Emma S. Rudge, Alex H. Y. Chan, Finian J. Leeper
, RSC Med. Chem.
, 2022
, 13
, 375
- Enhancing the stability of active pharmaceutical ingredients by the cocrystal strategy. Liyu Liu, Jian-Rong Wang, Xuefeng Mei
, CrystEngComm
, 2022
, 24
, 2002
- Promising approaches and kinetic prospects of the microbial degradation of pharmaceutical contaminants. S. Karishma, P. R. Yaashikaa, P. Senthil Kumar, R. Kamalesh, A. Saravanan, Gayathri Rangasamy
, Environ. Sci.: Adv.
, 2023
, 2
, 1488
- Direct observation of α- to β-glycine transformation during the ionic liquid-mediated crystallization process. Liangfei Ouyang, Tengfei Zheng, Liang Shen
, CrystEngComm
, 2018
, 20
, 2705
- Medicinal chemistry strategies for discovering antivirals effective against drug-resistant viruses. Yue Ma, Estrella Frutos-Beltrán, Dongwei Kang, Christophe Pannecouque, Erik De Clercq, Luis Menéndez-Arias, Xinyong Liu, Peng Zhan
, Chem. Soc. Rev.
, 2021
, 50
, 4514