Unlocking Catalyst Activation as a Critical Bottleneck in Cross-Coupling Reactions: Room-Temperature Couplings of Weak Nucleophiles Enabled by [Pd(1-MeNAP)TFA]<sub>2</sub> Precatalysts. [PDF]
Manna S +6 more
europepmc +1 more source
Synthesis of Naphthoquinones by Pd‐Catalyzed Heck–Matsuda Arylation of Lapachol
Direct Heck–Matsuda arylation of lapachol enables the efficient synthesis of diverse naphthoquinones under homogeneous and heterogeneous palladium catalysis. The methodology features broad substrate scope, gram‐scale applicability, and provides a practical platform for quinone diversification.
Breno U. de Abreu +13 more
wiley +1 more source
Recent advances in sulfur-containing flavors of garlic (<i>Allium sativum</i> L.): formation mechanisms, controlling factors and innovative processing technologies. [PDF]
Wu P, Dong T, Sun J, Chen H.
europepmc +1 more source
Selective N‐Functionalization of Pyrazoles
This review traces the evolution of regioselective N‐functionalization strategies for pyrazoles, a key class of nitrogen heterocycles widely used in medicinal chemistry. Due to rapid tautomerism, N‐functionalization often lacks selectivity, leading to poor and unpredictable regioisomeric outcomes.
Lucas Popek +2 more
wiley +1 more source
Influence of Fermentation and Curing on Residual Nitrite, Physico-Chemical, Volatile, Sensory, and Microbiological Properties of Sucuk Döner Kebab During Refrigerated and Frozen Storage. [PDF]
Sinan A +3 more
europepmc +1 more source
A nickel‐catalyzed three‐component reaction between arylaldehydes, butadiene, and malonates is developed yielding high functionalized homoallylic alcohols in a single step. No additional base is required and the reaction shows broad substrates compatibility with yields up to 96% and an exclusive selectivity toward the linear E‐isomer.
Anthony Saint Pol +7 more
wiley +1 more source
Three reversibly interconvertible redox states of boradigermaallyl: syntheses of radical allyl anion and allyl dianion. [PDF]
Miehe SF +5 more
europepmc +1 more source
Cysteine–fluorophore conjugates were efficiently prepared through a visible‐light‐driven thiol–ene approach employing solely organic photocatalysts. The reaction proceeds under mild, metal‐free conditions. The fluorophore scope includes mono‐ and dialkene‐functionalized naphthalene, naphthalimide, and aromatic diimide derivatives.
Julieth Bellaizac‐Riascos +4 more
wiley +1 more source
Visible‐light thiol–ene reaction mediated by 4CzIPN enables access to hydrolytically stable S‐linked glycoconjugates from levoglucosenone‐derived thiols (Y = 91% to quant. d.r. = up to >95:5) and conventional thio‐sugars (Y = 80% to quant. d.r. = up to >95:5).
Lorenzo Poletti +5 more
wiley +1 more source
Highly regio- and <i>E</i>-stereoselective C[double bond, length as m-dash]C bond transposition catalyzed by tris(benzhydryl) sodium calciate. Proof of synergy: one metal is good, but two are better. [PDF]
Koshelev IV +4 more
europepmc +1 more source

