Results 41 to 50 of about 1,345 (190)
Weak interaction of thieno[3,2‐b]pyridine with the kinase hinge region allows for design of highly selective inhibitors of underexplored kinases with variable binding modes. The newly identified chemical biology probe MU1920 targets the kinase Haspin with exquisite kinome‐wide selectivity.
Paula Martín Moyano +15 more
wiley +2 more sources
5,5′-Thiobis(3-bromoisothiazole-4-carbonitrile)
The reaction of sodium 2,2-dicyanoethene-1,1-bis(thiolate) with bromine (2 equiv.) in CCl4 gave 3,5-dibromoisothiazole-3-carbonitrile and 5,5′-thiobis(3-bromoisothiazole-4-carbonitrile) in 7% and 18% yields, respectively.
Andreas S. Kalogirou +1 more
doaj +1 more source
Intramolecular Carbene C-H Insertion Reactions of 2-Diazo-2-sulfamoylacetamides
The intramolecular C-H insertions of carbenes derived from 2-diazo-2-sulfamoylacetamides were studied. 2-Diazo-2-sulfamoylacetamides were first prepared from chloroacetyl chloride and secondary amines through acylation followed by sequential treatments ...
Chuqiang Que +4 more
doaj +1 more source
The study of the properties, chemical composition, and degradation patterns of rubber materials used in vehicle tires remains a complex and interdisciplinary task. Rubber for tires—more precisely, complex mixtures of elastomers containing fillers, plasticizers, binders, and other additives—is a condensed chemically active material, the composition and ...
Roman Tangalychev +3 more
wiley +1 more source
Alkylation of the reaction product of sodium 3-iminobutyronitrile and carbon disulfide produces alkyl 2-cyano-3-iminodithiobutyrates (1) in moderate yield, which on iodine oxidation afford 5-alkylthio-3-methylisothiazole-4-carbonitriles (2b-e).
HD Krebs, FC James
core +1 more source
Synthetic Strategies to Access Fluorinated Azoles
This review highlights recent synthetic strategies for introducing fluorine groups (mono‐, di‐, and trifluoromethylation) into 11 major azole classes, identifying research gaps to inform future innovations in materials science, medicinal chemistry, and biomedical research.
Mohammed K. Abd El‐Gaber +4 more
wiley +1 more source
The palladium-catalyzed reaction of 5-bromo-3-diethylamino-4-(4-methoxyphenyl)-isothiazole 1,1-dioxide (3) with a variety of vinyl-, aryl-, heteroaryl- and alkynylstannanes 4 provides a general and efficient method for the synthesis of 5-substituted ...
E. Erba +3 more
core +1 more source
Use of N‐heterocyclic carbenes (NHCs) to activate carbon and heteroatoms in aromatic compounds is reviewed based on key dearomative NHC‐bound intermediates, i.e., ortho‐quinodimethanes (o‐QDMs), ortho‐quinone methides (o‐QMs) and aza‐analogs (aza‐o‐QMs), aza‐fulvene and triaza‐diene intermediates.
Carmela De Risi +4 more
wiley +1 more source
Isothiazole dioxides have been shown to inhibit Trypanosoma brucei protein farnesyltransferase (PFTase) in isolated enzyme, but elicited only a minor effect on mammalian PFTase.
FERRI, NICOLA +5 more
core +1 more source
Photochemische Permutation von Indazolen zu Benzimidazolen
Hier stellen wir eine photochemische Strategie für die direkte Permutation von 1H‐ und 2H‐Indazolen zu Benzimidazolen vor. Dieser Ansatz beruht auf einem zweistufigen Mechanismus aus Tautomerisierung im angeregten Zustand und photochemischer Umlagerung, bietet einen breiten Anwendungsbereich, hohe Ausbeuten und funktionelle Gruppentoleranz und erhöht ...
Thiago dos Santos +5 more
wiley +1 more source

