Results 71 to 80 of about 12,572 (245)
C‐Terminal Functionalization Methods of Amino Acids, Peptides, and Proteins
C‐terminal functionalization offers powerful routes to peptide and protein diversification, yet epimerization, hydrolysis, and selectivity remain key challenges. This Review surveys enzymatic, decarboxylative, and condensation strategies, highlighting advances toward chemo‐ and regioselective, protecting‐group‐free, atom‐efficient methods applicable to
Jay Hanssens +3 more
wiley +1 more source
Asymmetric architecture was built for synergistic production of H2O2 and benzaldehyde. The reaction mechanism involves the synergistic utilization of electrons and holes, which jointly enables efficient oxygen activation to support the simultaneous production of two high‐value products.
Han Wang +7 more
wiley +1 more source
Intermediates in halogenation of 2-amino-thiazoles
Halogenation of 2-amino-thiazoles in various solvents to 2-amino-5-halogenated-thiazoles is ...
MEDICI, Alessandro, L. FORLANI
core
Herein we report a series of new benzimidazolium chlorides as N-heterocyclic carbene (NHC) ligand and their corresponding palladium(II)-NHC complexes with the general formula [PdCl2(NHC)(2)] were synthesized.
Murat Kaloğlu +3 more
core +1 more source
ABSTRACT Children, as a particularly vulnerable group, are more susceptible to these mutagens due to their developing immune systems, higher physiological vulnerability, and increased exposure through behaviors like outdoor play and hand‐to‐mouth activities. This review aims to investigate the relationship between these environmental exposures, genetic
Thiago Guedes Pinto +7 more
wiley +1 more source
This work demonstrates a layer‐bridging coordination strategy of Co single atoms in COFs that promotes the formation and utilization of triplet excited states. The introduction of Co single atoms induces pronounced energy‐level splitting and enhanced spin–orbit coupling, facilitating the generation of 1O2 and O2•– for efficient photocatalytic H2O2 ...
Guoen Tang +6 more
wiley +2 more sources
Synthetic routes to all possible regioisomeric mono- and bis(trimethylsilyl)thiazoles as well as to the tris-(trimethylsilyl) derivative via lithiation-silylation sequences of the thiazole ring followed by selective protodesilylation in some cases are ...
MEDICI, Alessandro +4 more
core +1 more source
Advancing Therapies for Mycobacterial Diseases: From Small Molecules to Host‐Directed Strategies
ABSTRACT The global burden of multidrug‐resistant tuberculosis (MDR‐TB) and the rising incidence of nontuberculous mycobacterial (NTM) infections highlight the urgent need for innovative therapeutic strategies. Current treatments are prolonged, toxic, and increasingly compromised by resistance and limited diagnostic capacity.
Tânia Silva +23 more
wiley +1 more source
The title compounds, C17H13N3OS2, (I), and C17H12BrN3OS2, (II), are potential active pharmaceutical ingredients. Compound (I) comprises two almost planar fragments. The first is the central (carbamothioyl)amide (r.m.s.
Ekaterina S. Gantimurova +6 more
doaj +1 more source
Preparation of thiazoles and benzothiazoles as possible anthelmintics
Derivatives of mercaptobenzothiazoles, benzothiazoles, and thiazoles have been prepared, most containing phenothiazine residues. Some of the compounds were very active against liver fluke (Fasciola hepatica) in vitro.
Mackie, Alexander, Misra, Anand L
core +1 more source

