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Substrate channel evolution of an esterase for the synthesis of cilastatin. Zheng-Jiao Luan, Fu-Long Li, Shuai Dou, Qi Chen, Xu-Dong Kong, Jiahai Zhou, Hui-Lei Yu, Jian-He Xu , Catal. Sci. Technol. , 2015 , 5 , 2622

Recent advances in the rational design and optimization of antibacterial agents. Jesse A. Jones, Kristopher G. Virga, Giuseppe Gumina, Kirk E. Hevener , Med. Chem. Commun. , 2016 , 7 , 1694

β-lactam/β-lactamase inhibitor combinations: an update. Kamaleddin H. M. E. Tehrani, Nathaniel I. Martin , Med. Chem. Commun. , 2018 , 9 , 1439

Recent advances and perspectives in the design and development of polymyxins. Francesc Rabanal, Yolanda Cajal , Nat. Prod. Rep. , 2017 , 34 , 886

The renewed challenge of antibacterial chemotherapy†. Daniela Niccolai, Luca Tarsi, Russell J. Thomas , Chem. Commun. , 1997 , 2333

A reusable, insoluble polymer-bound bis(oxazoline) (IPB-box) for highly enantioselective heterogeneous cyclopropanation reactions. Alessandro Mandoli, Simonetta Orlandi, Dario Pini, Piero Salvadori , Chem. Commun. , 2003 , 2466

Rapid detection of carbapenem-resistant Enterobacteriaceae using pH response based on vancomycin-modified Fe3O4@Au nanoparticle enrichment and the carbapenemase hydrolysis reaction. Jianmin Wang, Wei Yang, Qiling Peng, Daobin Han, Liangsheng Kong, Lu Fan, Min Zhao, Shijia Ding , Anal. Methods , 2020

N-Arylalkylbenzo[d]thiazole-2-carboxamides as anti-mycobacterial agents: design, new methods of synthesis and biological evaluation. Parth Shah, Tejas M. Dhameliya, Rohit Bansal, Manesh Nautiyal, Damodara N. Kommi, Pradeep S. Jadhavar, Jonnalagadda Padma Sridevi, Perumal Yogeeswari, Dharmarajan Sriram, Asit K. Chakraborti , Med. Chem. Commun. , 2014 , 5 , 1489

Homochiral metal–organic frameworks as heterogeneous catalysts. Andreea Gheorghe, Martijn A. Tepaske, Stefania Tanase , Inorg. Chem. Front. , 2018 , 5 , 1512

Synthesis of fused cyanopyrroles and spirocyclopropanes via addition of N-ylides to chalconimines. Siba Prasad Midya, Elumalai Gopi, Nishikant Satam, Irishi N. N. Namboothiri , Org. Biomol. Chem. , 2017 , 15 , 3616