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Divergent response of homologous ATP sites to stereospecific ligand fluorination for selectivity enhancement. Alpesh Ramanlal Patel, Ari Hardianto, Shoba Ranganathan, Fei Liu , Org. Biomol. Chem. , 2017 , 15 , 1570

Sustainable production of pharmaceutical, nutraceutical and bioactive compounds from biomass and waste. Claudia Espro, Emilia Paone, Francesco Mauriello, Roberto Gotti, Elisa Uliassi, Maria Laura Bolognesi, Daily Rodríguez-Padrón, Rafael Luque , Chem. Soc. Rev. , 2021 , 50 , 11191

Synthon identification in co-crystals and polymorphs with IR spectroscopy. Primary amides as a case study. Arijit Mukherjee, Srinu Tothadi, Shaunak Chakraborty, Somnath Ganguly, Gautam R. Desiraju , CrystEngComm , 2013 , 15 , 4640

Tuning mechanical behaviour by controlling the structure of a series of theophylline co-crystals. Shubhangi Kakkar, Biswajit Bhattacharya, C. Malla Reddy, Soumyajit Ghosh , CrystEngComm , 2018 , 20 , 1101

Biodegradation of bromoxynil using the cascade enzymatic system nitrile hydratase/amidase from Microbacterium imperiale CBS 498-74. Comparison between free enzymes and resting cells. Fabrizia Pasquarelli, Agata Spera, Laura Cantarella, Maria Cantarella , RSC Adv. , 2015 , 5 , 36913

Design of 4-aminobenzoic acid two-component molecular crystals: prediction and experiments. Alex N. Manin, Ksenia V. Drozd, Andrei V. Churakov, German L. Perlovich , CrystEngComm , 2019 , 21 , 2119

Cocrystals of the antiandrogenic drug bicalutamide: screening, crystal structures, formation thermodynamics and lattice energies. Artem O. Surov, Katarzyna A. Solanko, Andrew D. Bond, Annette Bauer-Brandl, German L. Perlovich , CrystEngComm , 2016 , 18 , 4818

NHC-catalyzed silylative dehydration of primary amides to nitriles at room temperature. Pradip Kumar Hota, Subir Maji, Jasimuddin Ahmed, N. M. Rajendran, Swadhin K. Mandal , Chem. Commun. , 2020 , 56 , 575

The complete conversion of the highly hindered ester, 2-carbamoylphenyl mesitoate, into the highly hindered amide, mesitamide, via base-catalysed intramolecular nucleophilic amide-group participation. R. Malcolm Topping, David E. Tutt , J. Chem. Soc. B , 1967 , 1346

A facile hybrid ‘flow and batch’ access to substituted 3,4-dihydro-2H-benzo[b][1,4]oxazinones. Andrew J. S. Lin, Cecilia C. Russell, Jennifer R. Baker, Shelby L. Frailey, Jennette A. Sakoff, Adam McCluskey , Org. Biomol. Chem. , 2016 , 14 , 8732