Results 191 to 200 of about 33,790 (273)

Responding to reports of nitazene toxicity in Australia

open access: yes
Medical Journal of Australia, Volume 222, Issue 5, Page 216-219, March 2025.
Brendan Clifford   +5 more
wiley   +1 more source

Genetic Mapping of the Powdery Mildew Resistance Gene Pm13 on Oat (Avena sativa) Chromosome 1D

open access: yesPlant Breeding, Volume 144, Issue 3, Page 387-398, June 2025.
ABSTRACT Powdery mildew, caused by the biotrophic fungus Blumeria graminis DC. f. sp. avenae, is a widespread disease of oats, especially in the temperate regions of Western and Central Europe, and the use of resistant varieties is the most sustainable way to ensure stable yields.
Selma Schurack   +10 more
wiley   +1 more source

Syntheses of Benzimidazole Derivatives from Aromatic Trichloromethyl Compounds with Aromatic o-Diamines

open access: bronze, 1974
Kazuyuki Takahashi   +5 more
openalex   +2 more sources

Carbazole Framework as Functional Scaffold for the Design of Synthetic Receptors

open access: yesChemistry – A European Journal, Volume 31, Issue 30, May 27, 2025.
Carbazole‐based receptors play a crucial role in supramolecular chemistry, due to their unique geometry, photophysical properties, strong hydrogen bonding features, and versatility. This review examines prominent examples, focusing on how structural modifications shape binding affinity and selectivity for various guests, showcasing the potential of ...
Alessio Carioscia   +6 more
wiley   +1 more source

Click Conjugates of Artificial Ribonucleases: Sequence Specific Cleavage with Multiple Turnover

open access: yesChemistry – A European Journal, Volume 31, Issue 30, May 27, 2025.
A trisbenzimidazole catalyst was attached to central positions of DNA and DNA‐LNA oligonucleotides. The resulting conjugates bind complementary RNA strands and cleave them with multiple turnover and substrate half‐lives down to 3.5 hours. Up to 98.8% of cleavage occurs in a single site.
Sandra Weber   +4 more
wiley   +1 more source

Recent Advances in the α‐Hydrazination (α‐Amination) of Carbonyl Compounds

open access: yesEuropean Journal of Organic Chemistry, Volume 28, Issue 17, May 21, 2025.
In recent years, notable progress has been achieved in the α‐hydrazination (α‐amination) of carbonyl compounds, especially in the direct asymmetric electrophilic α‐hydrazination with dialkyl azodicarboxylates. This review summarizes all the methods that appeared over the past decade, categorized based on the type of the reactive chiral intermediate ...
Dina Scarpi   +2 more
wiley   +1 more source

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