Functional and Network PHAs via Stereoselective Polymerization and Tailored Post‐Transformation
Catalyst‐controlled stereoselective (co)polymerization of functionalized lactones produces vinyl‐, allyl‐, and propargyl‐functionalized PHAs with high syndiotacticity and a broad applicable temperature window, which can be further transformed into crosslinked PHA thermosets, elastic supramolecular networks, and functional grafts. ABSTRACT Incorporation
Ruirui Li +6 more
wiley +1 more source
Carbonylative Synthesis of β-Trifluoromethylated Heterocyclic Ketones through 1,2-Trifluoromethylation and Minisci Carbonylation of Alkenes. [PDF]
Miao RG, A RH, Wu XF.
europepmc +1 more source
Katalysatoren, die aus dem Trifluoroacetat‐verbrückten Methylnaphthyl‐Palladium‐Dimer [Pd(1‐MeNAP)TFA]2 und Biarylphosphin‐Liganden generiert werden, in Kombination mit der Base LiHMDS, fördern α‐Arylierungsreaktionen verschiedener Enolate mit nicht‐aktivierten Arylfluoriden bei Raumtemperatur.
Nele Krüger +4 more
wiley +1 more source
The Synthesis of Tertiary Alkylamines from Alkyl-Substituted Alkenes Using Amine Umpolung Strategy. [PDF]
Nakatsuka S +3 more
europepmc +1 more source
Taming a Blue Gas—Structure and Chemistry of Hexafluorothioacetone
Hexafluorothioacetone (1), a blue gas at r.t., was synthesized by flash vacuum pyrolysis of its cyclic dimer at 660°C. We discuss fundamental properties of elusive 1, including single‐crystal structure and nuclear magnetic resonance spectroscopy, despite its tendency to dimerize even at –74°C.
Hennes Günther +3 more
wiley +1 more source
General Difluoroalkylation of Unactivated Alkenes Via Allylic Mizoroki-Heck Coupling. [PDF]
Wang J +5 more
europepmc +1 more source
Unified Synthesis of Unconventional α‐Polyhalogenated Amines Through Hydroaminoalkylation
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
Markovnikov hydroamination of terminal alkenes by phosphine redox catalysis. [PDF]
Fan F +3 more
europepmc +1 more source
A Tutorial on the Mechanisms of Group 9 Transition-Metal-Catalyzed Asymmetric Olefin Hydrogenation. [PDF]
Mendelsohn LN, Chirik PJ.
europepmc +1 more source

