Transition-metal-catalyzed nitrene transfer reactions are typically performed in organic solvents under inert and anhydrous conditions due to the involved air and water-sensitive nature of reactive intermediates.
Dóra Lakk-Bogáth +3 more
doaj +1 more source
Enantioselective dioxytosylation of styrenes using lactate-based chiral hypervalent iodine(III)
A series of optically active hypervalent iodine(III) reagents prepared from the corresponding (R)-2-(2-iodophenoxy)propanoate derivative was employed for the asymmetric dioxytosylation of styrene and its derivatives.
Morifumi Fujita +2 more
doaj +1 more source
Electrochemical N-olefination for the regio- and stereo-selective synthesis of vinyl azoles
A selenium-catalyzed electrosynthesis involving regio- and stereo-selective N-olefination of azoles was developed. The room-temperature reaction was efficient (up to 97 % yield) and compatible with various styrenes and azoles.
Kejun Lin +3 more
doaj +1 more source
Molybdooxaziridine-Molybdodioxirane Tandem Catalysis: Synthesis of α-Nitrosulfones from Styrenes. [PDF]
Doran JM +3 more
europepmc +1 more source
Visible light-mediated 1,2-difunctionalization reactions involving 4-cyanopyridines. [PDF]
Raymand P +5 more
europepmc +1 more source
Pentafluoroethyl Sulfoximine Reagent for the Photocatalytic Pentafluoroethylation-Difunctionalization of Styrene Derivatives. [PDF]
Lin L +6 more
europepmc +1 more source
Recent Advances in Organocatalytic Kinetic Resolution for the Synthesis of Axially Chiral Compounds. [PDF]
Cui L, Zheng Y.
europepmc +1 more source
Identification of HOTf-Driven Brønsted Acid Catalysis in the AuCl<sub>3</sub>/AgOTf System for the Hydroalkylation of Styrene. [PDF]
Mahdian A +4 more
europepmc +1 more source
Arylation of Olefins with N-Unprotected Bromobisindole Ethanamines: Expanding the Scope of the Mizoroki-Heck Reaction. [PDF]
Buono A +5 more
europepmc +1 more source
<i>cis</i>-Selective Direct Halocyclopropanation of Alkenes Mediated by Nucleophilic Cobalt Photocatalysis. [PDF]
Teye-Kau JHG, Pauze M, Pitre SP.
europepmc +1 more source

