Alkyl amines join the substitution toolbox as chemists strip nitrogen to forge carbon bonds
A Nature Synthesis study reports a deaminative nucleophilic substitution platform that converts alkyl amines into direct alkylation reagents for forging ...
A Nature Synthesis study reports a deaminative nucleophilic substitution platform that converts alkyl amines into direct alkylation reagents for forging ...
Chemists report two simplified routes to trifluoromethylpyrazoles, including a one-hour Aliquat 336-catalyzed coupling that avoids major side products.
Chemists report a soluble quinacridone photocatalyst that oxidizes sulfides to sulfoxides with oxygen under green light at 0.1 mol percent ...
Chemists report a scalable multistep synthesis of indole–benzimidazole–piperazine carboxamide hybrids, optimized bond by bond and computationally profiled without claims of ...
An iridium catalytic system using multiple noncovalent interactions enables para-C–H activation and borylation of free aromatic carboxylic acids without directing ...
Rice University researchers used iron, sulfur, purple light and carboxylic acids to enable carbon-carbon bond formation through anti-Markovnikov alkene hydroalkylation.
A review of laccase catalysis shows how oxygen-driven enzymes can support greener oxidation, coupling, cyclization and polymerization reactions when enzyme, ...
KAIST chemists have built an automated platform that combines robots, continuous-flow chemistry and visible light to synthesize drug candidate compounds ...
Researchers at The University of Osaka have developed a rhodium-catalyzed reaction that uses a single carbon atom from a PINC ...
Chemists in Tokyo have achieved the enantioselective synthesis of a giant π-extended carbohelicene using sequence-controlled quadruple cycloadditions, yielding an all-carbon ...
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© 2025 Scienmag - Science Magazine