Correction: Review of the novel antifungal drug olorofim (F901318). [PDF]
Vanbiervliet Y +5 more
europepmc +1 more source
Molecular mechanisms governing antifungal drug resistance. [PDF]
Lee Y, Robbins N, Cowen LE.
europepmc +1 more source
A one‐pot protocol to synthesize reactive benzyl‐ and allyl‐halide‐substituted (dihydro)naphthalenes from 2,3‐aryl‐1,3‐butadiene substrates and halogenated alkanes has been developed, using [Cp*RuCl(PPh3)2] as the catalyst. Mechanistic studies revealed an atom transfer radical addition and radical benzannulation sequence, followed by HCl elimination ...
Nicole S. van Leeuwen +9 more
wiley +1 more source
Real-world correlation between therapeutic drug monitoring and clinical outcomes of the antifungal drug posaconazole: a single-center retrospective cohort study. [PDF]
Yi Q +11 more
europepmc +1 more source
Advances in Antifungal Development: Discovery of New Drugs and Drug Repurposing
Jong H. Kim +2 more
openalex +1 more source
Versatile Palladium‐Catalyzed C‐H Arylation of Fluoroarenes with 2‐Chloropyridine Derivatives
Direct C─H arylation of fluoroarenes with 2‐chloropyridines is enabled by a simple Pd/SPhos system in isopropyl acetate. The method uses inexpensive reactants and shows broad scope and high yields. DFT computations explain reactivity and selectivity.
Federico Belnome +6 more
wiley +1 more source
Signaling pathways governing the pathobiological features and antifungal drug resistance of <i>Candida auris</i>. [PDF]
Cha H, Won D, Bahn Y-S.
europepmc +1 more source
Therapeutic tools for oral candidiasis: Current and new antifungal drugs
Guillermo Quindós +6 more
openalex +1 more source
Antifungal drugs: What brings the future? [PDF]
Ruth Van Daele +6 more
openalex +1 more source
Identification of Natural Isonitriles Through Ligation to an Azomethine Imine Probe
The azomethine imine (AMI)–isonitrile (NC) ligation allowed for the chemoselective detection of natural isonitriles in bacteria and fungi. The reactivity‐based screening establishes a new stereogenic center, thereby allowing for facile distinction between chiral and achiral isonitriles. The work also unraveled a unique reactivity of isonitriles bearing
Maurice P. Biedermann +6 more
wiley +1 more source

