Wang, Rong published the artcileOxime-derived palladacycle Immobilized in an Ionic Liquid Brush as an Efficient and Reusable Catalyst for Mizoroki-Heck Reaction in Neat Water, Recommanded Product: (E)-3-(3-Nitrophenyl)acrylic acid, the publication is Applied Organometallic Chemistry (2019), 33(11), e5226, database is CAplus.
An efficient and reusable heterogeneous catalyst with oxime-derived palladacycle immobilized in an ionic liquid brush was synthesized and an environmentally-friendly procedure was developed for coupling aryl iodides and bromides with acrylic acid to get corresponding cinnamic acid derivatives I [R = H, 2-Me, 4-OMe, etc.]. These reactions were conducted in neat water under aerobic conditions with water-insoluble or even solid aryl halides and they proceeded smoothly and cleanly without any organic co-solvent or other additives. The ionic liquid brush could be easily recovered and reused at least five times without significant loss of activity. The protocol was the advantages of excellent yields, environmental friendliness and catalyst recyclability.
Applied Organometallic Chemistry published new progress about 1772-76-5. 1772-76-5 belongs to catalysis-chemistry, auxiliary class Benzenes, name is (E)-3-(3-Nitrophenyl)acrylic acid, and the molecular formula is C18H28B2O4, Recommanded Product: (E)-3-(3-Nitrophenyl)acrylic acid.
Referemce:
https://courses.lumenlearning.com/boundless-chemistry/chapter/catalysis/,
Catalysis – Wikipedia