Oxetanes: recent advances in synthesis, reactivity, and medicinal chemistry

JA Bull, RA Croft, OA Davis, R Doran… - Chemical …, 2016 - ACS Publications
The four-membered oxetane ring has been increasingly exploited for its contrasting
behaviors: its influence on physicochemical properties as a stable motif in medicinal …

Metabolism, biochemical actions, and chemical synthesis of anticancer nucleosides, nucleotides, and base analogs

J Shelton, X Lu, JA Hollenbaugh, JH Cho… - Chemical …, 2016 - ACS Publications
Nucleoside, nucleotide, and base analogs have been in the clinic for decades to treat both
viral pathogens and neoplasms. More than 20% of patients on anticancer chemotherapy …

Fluorine-a small magic bullet atom in the drug development: perspective to FDA approved and COVID-19 recommended drugs

G Chandra, DV Singh, GK Mahato, S Patel - Chemical Papers, 2023 - Springer
During the last twenty years, organic fluorination chemistry established itself as an important
tool to get a biologically active compound. This belief can be supported by the fact that every …

The expanded genetic alphabet

DA Malyshev, FE Romesberg - … Chemie International Edition, 2015 - Wiley Online Library
All biological information, since the last common ancestor of all life on Earth, has been
encoded by a genetic alphabet consisting of only four nucleotides that form two base pairs …

C-Nucleosides to be revisited: Miniperspective

E De Clercq - Journal of medicinal chemistry, 2016 - ACS Publications
Two new C-nucleoside analogues, BCX4430, an imino-C-nucleoside, and GS-6620, a
phosphoramidate derivative of 1′-cyano-2′-C-methyl-4-aza-7, 9-dideazaadenosine C …

A short de novo synthesis of nucleoside analogs

M Meanwell, SM Silverman, J Lehmann, B Adluri… - Science, 2020 - science.org
Nucleoside analogs are commonly used in the treatment of cancer and viral infections. Their
syntheses benefit from decades of research but are often protracted, unamenable to …

Fluorinated nucleosides: synthesis, modulation in conformation and therapeutic application

S Pal, G Chandra, S Patel, S Singh - The Chemical Record, 2022 - Wiley Online Library
Over the last twenty years, fluorination on nucleoside has established itself as the most
promising tool to use to get biologically active compounds that could sustain the clinical trial …

Chemoselective and Diastereoselective Synthesis of C‐Aryl Nucleoside Analogues by Nickel‐Catalyzed Cross‐Coupling of Furanosyl Acetates with Aryl Iodides

Y Li, Z Wang, L Li, X Tian, F Shao, C Li - Angewandte Chemie, 2022 - Wiley Online Library
Canonical nucleosides are vulnerable to enzymatic and chemical degradation, yet their
stable mimics—C‐aryl nucleosides—have demonstrated potential utility in medicinal …

Pyrrolo[2,3‐d]pyrimidine (7‐deazapurine) as a privileged scaffold in design of antitumor and antiviral nucleosides

P Perlíková, M Hocek - Medicinal Research Reviews, 2017 - Wiley Online Library
Deazapurine (pyrrolo [2, 3‐d] pyrimidine) nucleosides are important analogues of biogenic
purine nucleosides with diverse biological activities. Replacement of the N7 atom with a …

Chemoselective reactions for the synthesis of glycoconjugates from unprotected carbohydrates

K Villadsen, MC Martos‐Maldonado, KJ Jensen… - …, 2017 - Wiley Online Library
Glycobiology is the comprehensive biological investigation of carbohydrates. The study of
the role and function of complex carbohydrates often requires the attachment of …