Results 131 to 140 of about 26,606 (255)
Journal of the Brazilian Chemical Society, 1999 Experiments towards the diastereoselective coupling of new malonic acid amides synthesized with commercially available chiral amines [(S)-(+)-1-cyclohexylethylamine and (R)-(+)-1-phenylethylamine] as chiral auxiliaries were performed through Kolbe ...
Goulart Marília O.F. +1 more
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Advances in Unconventional and Sustainable Synthetic Approaches to Benzopyran Scaffolds
The Chemical Record, EarlyView.This review provides a comprehensive and critical analysis of low‐impact synthetic methodologies reported in the last 8 years (2018–2026) for the construction of benzopyran‐derived scaffolds, such as coumarins, flavones, chromones, chromenes, and chromanes. The benzopyran scaffold is a versatile family of heterocycles found in a wide range of bioactive
Nathalia B. Sá +4 more
wiley +1 more source
Oxaziridines: Versatile Reagents in Modern Organic Synthesis
The Chemical Record, EarlyView.Being capable of transferring an O atom and N‐group/atom, oxaziridines are considered multitasking agents. These are employed for diverse organic transformations, such as epoxidation of olefins, α‐ and γ‐hydroxylation/amination of carbonyl compounds, oxidation of sulfides, [3+2]cycloaddition with unsaturated systems.
Ajeet Chandra +2 more
wiley +1 more source
Sodium Hypochlorite Pentahydrate in Organic Synthesis and Beyond
Chemistry–Methods, Volume 6, Issue 10, October 2026.Sodium hypochlorite pentahydrate emerges as a versatile, stable, and practical oxidant for organic synthesis. This review highlights its unique reactivity, broad synthetic applications, and growing impact on sustainable oxidation chemistry, providing a comprehensive overview of recent advances and future opportunities. Sodium hypochlorite pentahydrate (
Masayuki Kirihara +2 more
wiley +1 more source
Angewandte Chemie, Volume 138, Issue 38, 14 September 2026.A stereoselective functionalization method of cyclic imines under mild organocatalytic conditions was developed. Bifunctional cinchona alkaloid catalysts combined with carefully optimized reaction conditions to suppress background reactivity enabled highly enantio‐ and diastereoselective addition reactions of malonates to cyclic imines.
Frederic Kölblin, Helma Wennemers
wiley +2 more sources
Cobalt‐Catalyzed C(sp3)H Carbonylation Enabled by Mo(CO)6
European Journal of Organic Chemistry, Volume 29, Issue 36, 24 September 2026.Cobalt‐catalyzed carbonylative C(sp3)H cyclization of aliphatic amides using Mo(CO)6 as a solid CO surrogate enables efficient access to substituted succinimides under operationally simple conditions. The carbonylation of unactivated C(sp3)H bonds represents an attractive strategy for the synthesis of valuable carbonyl‐containing compounds.
Emma Duro +4 more
wiley +1 more source
π‐Extended Silyl Enolates as Emerging Platforms in Radical Chemistry
European Journal of Organic Chemistry, Volume 29, Issue 36, 24 September 2026.This review covers the emerging role of π‐extended silyl polyenol ethers in radical chemistry. It highlights their versatile roles as electron‐rich SOMOphiles, silyl radical cation precursors, and nucleophilic partners in radical–polar crossover manifolds, while considering recent advances in photoredox catalysis, electrochemistry, and transition metal‐
Debora Guazzetti +3 more
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A Straightforward Synthesis of Benzestrol by Matteson Homologation Using Chiral Benzyl Carbamates
European Journal of Organic Chemistry, Volume 29, Issue 36, 24 September 2026.Benzestrol can easily be obtained stereoselectively via Matteson reaction using chiral Boronic esters and chiral benzyl carbamates. A straightforward and highly stereoselective synthesis of the non‐steroidal estrogen benzestrol is described based on Matteson homologations.
Max Benjamin Becker, Uli Kazmaier
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CHIMIA, 1993 Optically active 3-hydroxybutyric and 3-hydroxyhexanoic acids were transformed into 3,4-disubstituted and 3,3,4-trisubstituted 2-oxetanones using two different approaches.
Günter Scherowsky, Michael Sefkow
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Unified Synthesis of Unconventional α‐Polyhalogenated Amines Through Hydroaminoalkylation
Angewandte Chemie International Edition, Volume 65, Issue 38, 14 September 2026.A unified, redox‐neutral method that transforms alkenes and alkynes into α‐polyhalomethyl amines using stable hemiaminal reagents is reported. This approach enables access to CF3, CF2H, CF2Cl, and CFClH motifs, expanding halogenated amine space with broad substrate scope, functional group tolerance, and applicability to late‐stage modification of drug ...
Angela K. Hofmeister +9 more
wiley +1 more source