32664-13-4Relevant articles and documents
Copper Photosensitizers Containing P^N Ligands and Their Influence on Photoactivity and Stability
Giereth, Robin,Frey, Wolfgang,Junge, Henrik,Tschierlei, Stefanie,Karnahl, Michael
, p. 17432 - 17437 (2017)
Driven by the intention to improve classic heteroleptic copper photosensitizers two novel Cu(I) complexes applying a hetero-bidentate P^N ligand were prepared. A combined photophysical, electrochemical, and theoretical study gives insights into structure–activity relationships and revealed an increased absorptivity. Both complexes were tested for the light-driven production of H2.
Sulfoxide ligand metal catalyzed oxidation of olefins
-
, (2019/05/09)
The enantioselective synthesis of isochroman motifs has been accomplished via Pd(II)-catalyzed allylic C—H oxidation from terminal olefin precursors. Critical to the success of this goal was the development and utilization of a novel chiral aryl sulfoxide-oxazoline (ArSOX) ligand. The allylic C—H oxidation reaction proceeds with the broadest scope and highest levels asymmetric induction reported to date (avg. 92% ee, 13 examples ≥90% ee). Additionally, C(sp3)-N fragment coupling reaction between abundant terminal olefins and N-triflyl protected aliphatic and aromatic amines via Pd(II)/sulfoxide (SOX) catalyzed intermolecular allylic C—H amination is disclosed. A range of 52 allylic amines are furnished in good yields (avg. 76%) and excellent regio- and stereoselectivity (avg. >20:1 linear:branched, >20:1 E:Z). For the first time, a variety of singly activated aromatic and aliphatic nitrogen nucleophiles, including ones with stereochemical elements, can be used in fragment coupling stiochiometries for intermolecular C—H amination reactions.
C-H to C-N Cross-Coupling of Sulfonamides with Olefins
Ma, Rulin,Christina White
, p. 3202 - 3205 (2018/03/13)
Cross-coupling of nitrogen with hydrocarbons under fragment coupling conditions stands to significantly impact chemical synthesis. Herein, we disclose a C(sp3)-N fragment coupling reaction between terminal olefins and N-triflyl protected aliphatic and aromatic amines via Pd(II)/SOX (sulfoxide-oxazoline) catalyzed intermolecular allylic C-H amination. A range of (56) allylic amines are furnished in good yields (avg. 75%) and excellent regio- and stereoselectivity (avg. >20:1 linear:branched, >20:1 E:Z). Mechanistic studies reveal that the SOX ligand framework is effective at promoting functionalization by supporting cationic π-allyl Pd.