Results 21 to 30 of about 4,762 (102)
An efficient mechanochemical route for diphenyleneiodonium (DPI) salt synthesis is reported which offers a sustainable and solvent‐free alternative. The solid‐state reactivities of the reported DPI salts were also assessed with the help of morphology predictions and Hirshfeld surface analysis computations to understand the effect of crystal morphology,
Ipsha Shruti, Tejender S. Thakur
wiley +1 more source
The introduction of an isopeptide bond at the lysine residues in the backbone of Esc(1‐21) led to the generation of five analogs. Among these, Esc(1‐21)ε20 showed the most promising features, having antimicrobial activity comparable with those of the parent peptide, a lower cytotoxicity, and a higher stability to proteolytic degradation.
Bruno Casciaro +11 more
wiley +1 more source
An umpolung strategy allowing the use of stilbenes as electrophiles in substitution reactions is developed that relies on a combination of m‐chloroperbenzoic acid and hexafluoroisopropanol. This new step‐economic approach gives rise to benzhydryl derivatives by the use of different nitrogenated, oxygenated, and sulfur‐ and carbon‐based nucleophiles ...
Francisco J. Sierra‐Molero +3 more
wiley +1 more source
Synthesis of Benzodithieno[5.5.5.6]Fenestranes: Unexpected Epimerization and Regiochemical Outcomes
Isomeric [5.5.5.6]fenestranes annulated with one benzene and two thiophene rings are accessible via di‐2‐ and di‐3‐thienylspirane intermediates. The key double cyclization step involves surprising stereoselectivity and regioselectivity. In particular, cis‐di(2‐thienyl)spirane precursors lead to the all‐cis‐fenestrane skeleton by an unexpected acid ...
Björn Bredenkötter +5 more
wiley +1 more source
Advances in Metal‐Free Transamidation: A Sustainable Approach to Amide Bond Formation
This review highlights the recent developments of transamidation reactions under metal‐free reaction conditions. Various amines including weak nucleophilic amines such as aromatic amines have been used to achieve the transamidation reactions under mild and relatively green reaction conditions. Abstract The amide functionalities are a crucial functional
Niharan Sivaraj +2 more
wiley +1 more source
Abstracts submitted to the ‘EACR 2025 Congress: Innovative Cancer Science’, from 16–19 June 2025 and accepted by the Congress Organising Committee are published in this Supplement of Molecular Oncology, an affiliated journal of the European Association for Cancer Research (EACR).
wiley +1 more source
Acid-promoted dehydroxylation coupling of aryl alcohols with 1,3-dicarbonyls and sulfonamides. [PDF]
Liang J +5 more
europepmc +1 more source
Total Synthesis and Anticancer Study of (+)-Verticillin A. [PDF]
Knauss W +4 more
europepmc +1 more source
Programmable Strategies for the Conversion of Aldehydes to Unsymmetrical (Deuterated) Diarylmethanes and Diarylketones. [PDF]
Gavit VR +4 more
europepmc +1 more source
Enantioconvergent Synthesis of Diarylmethane Drugs via Privileged Benzhydrol Intermediates. [PDF]
Frank E +4 more
europepmc +1 more source

