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- Chemoenzymatic total synthesis of rotigotine via IRED-catalyzed reductive amination. Dongyu Tang, Yaqing Ma, Jinping Bao, Shushan Gao, Shuli Man, Chengsen Cui
, Org. Biomol. Chem.
, 2024
- Frontiers of molecular crystal structure prediction for pharmaceuticals and functional organic materials. Gregory J. O. Beran
, Chem. Sci.
, 2023
, 14
, 13290
- Reductive aminations by imine reductases: from milligrams to tons. Amelia K. Gilio, Thomas W. Thorpe, Nicholas Turner, Gideon Grogan
, Chem. Sci.
, 2022
, 13
, 4697
- How many ritonavir cases are there still out there?. Marcus A. Neumann, Jacco van de Streek
, Faraday Discuss.
, 2018
, 211
, 441
- Strategies for the design of nanoparticles: starting with long-circulating nanoparticles, from lab to clinic. Ruyi Wang, Zhongtao Zhang, Bowen Liu, Jingwei Xue, Fulei Liu, Tongzhong Tang, Wenyuan Liu, Feng Feng, Wei Qu
, Biomater. Sci.
, 2021
, 9
, 3621
- Catalytic asymmetric transformations of oxa- and azabicyclic alkenes. Sundaravel Vivek Kumar, Andy Yen, Mark Lautens, Patrick J. Guiry
, Chem. Soc. Rev.
, 2021
, 50
, 3013
- Ir–Biaryl phosphite–oxazoline catalyst libraries: a breakthrough in the asymmetric hydrogenation of challenging olefins. Maria Biosca, Oscar Pàmies, Montserrat Diéguez
, Catal. Sci. Technol.
, 2020
, 10
, 613
- Raman mapping of fentanyl transdermal delivery systems with off-label modifications. Teng Xu, Huzeyfe Yilmaz, Daniel R. Willett, Caroline Strasinger, Jason D. Rodriguez, David A. Keire, Anna M. Wokovich
, Analyst
, 2020
, 145
, 953
- The curious case of (caffeine)·(benzoic acid): how heteronuclear seeding allowed the formation of an elusive cocrystal. Dejan-Krešimir Bučar, Graeme M. Day, Ivan Halasz, Geoff G. Z. Zhang, John R. G. Sander, David G. Reid, Leonard R. MacGillivray, Melinda J. Duer, William Jones
, Chem. Sci.
, 2013
, 4
, 4417
- Productivity enhancement of CC bioreductions by coupling the in situ substrate feeding product removal technology with isolated enzymes. Elisabetta Brenna, Francesco G. Gatti, Daniela Monti, Fabio Parmeggiani, Alessandro Sacchetti
, Chem. Commun.
, 2012
, 48
, 79