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- In silico analysis of SARS-CoV-2 papain-like protease potential inhibitors. Samia A. Elseginy, Manal M. Anwar
, RSC Adv.
, 2021
, 11
, 38616
- Large ring-forming alkylations provide facile access to composite macrocycles. Tristan E. Rose, Kenneth V. Lawson, Patrick. G. Harran
, Chem. Sci.
, 2015
, 6
, 2219
- Biocatalytic routes to anti-viral agents and their synthetic intermediates. Sjoerd Slagman, Wolf-Dieter Fessner
, Chem. Soc. Rev.
, 2021
, 50
, 1968
- Highlights from ASMC'13 – Advances in Synthetic and Medicinal Chemistry – May 5–8 2013, Moscow, Russia. Edmond Differding
, Med. Chem. Commun.
, 2013
, 4
, 1138
- Concise asymmetric synthesis of a (1R,2S)-1-amino-2-vinylcyclopropanecarboxylic acid-derived sulfonamide and ethyl ester. Sha Lou, Nicolas Cuniere, Bao-Ning Su, Lindsay A. Hobson
, Org. Biomol. Chem.
, 2013
, 11
, 6796
- Macrocyclization via C–H functionalization: a new paradigm in macrocycle synthesis. Saumitra Sengupta, Goverdhan Mehta
, Org. Biomol. Chem.
, 2020
, 18
, 1851
- Importance and synthesis of benzannulated medium-sized and macrocyclic rings (BMRs). Altaf Hussain, S. K. Yousuf, Debaraj Mukherjee
, RSC Adv.
, 2014
, 4
, 43241
- 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
- The Q41R mutation in the HCV-protease enhances the reactivity towards MAVS by suppressing non-reactive pathways. Chen Zheng, Markus Schneider, Antoine Marion, Iris Antes
, Phys. Chem. Chem. Phys.
, 2022
, 24
, 2126
- Targeting eukaryotic proteases for natural products-based drug development. Fatma H. Al-Awadhi, Hendrik Luesch
, Nat. Prod. Rep.
, 2020
, 37
, 827