Aryldipalladium example sentences

Related (5): Palladium, Aryl, Dipalladium, Catalyst, Cross-coupling

"Aryldipalladium" Example Sentences

1. Aryldipalladium compounds are often used as catalysts in organic synthesis.
2. The coupling of aryl halides with terminal alkynes can be achieved using aryldipalladium catalysts.
3. The mechanism of aryl halide oxidations with aryldipalladium complexes has been extensively studied.
4. Aryldipalladium compounds are typically prepared by the reaction of palladium salts with aryl halides.
5. The use of aryldipalladium catalysts has significantly improved the efficiency of cross-coupling reactions.
6. The preparation of aryldipalladium catalysts often involves the use of ligands to increase their reactivity.
7. Aryldipalladium compounds are known to be highly effective in promoting carbon-carbon bond formation.
8. Cross-coupling reactions facilitated by aryldipalladium catalysts have become increasingly popular in recent years.
9. Advances in the design of aryl halide substrates have led to greater efficiencies in arylpalladation reactions using aryldipalladium catalysts.
10. Zinc-copper exchange reactions are commonly used to activate aryl chlorides for use in aryldipalladium catalysis.
11. The use of chiral ligands in aryldipalladium catalysis has enabled highly selective formation of products.
12. Aryldipalladium catalysts have been used in a wide range of applications, including pharmaceuticals and agrochemicals.
13. Aryldipalladium complexes have been shown to be effective in the preparation of novel polymers with unique properties.
14. The regioselectivity of arylpalladation reactions using aryldipalladium catalysts can be strongly influenced by the choice of substrate.
15. Aryldipalladium-catalyzed cross-coupling reactions have found application in the synthesis of natural products and other complex molecules.
16. The use of aryl triflates as substrates in aryldipalladium catalysis can improve yields and selectivity.
17. Palladium-catalyzed C-H arylation reactions are typically carried out using aryldipalladium catalysts.
18. Aryldipalladium-catalyzed Suzuki-Miyaura couplings have become one of the most widely used methods for carbon-carbon bond formation.
19. The development of ligand-free aryldipalladium catalysts has opened up new possibilities for cross-coupling reactions.
20. Aryldipalladium catalysis can be used for the preparation of highly diverse compound libraries.
21. The use of aryldipalladium catalysts in aqueous media has been investigated to reduce environmental impact.
22. The search for more effective and sustainable aryldipalladium catalysts is an active area of research.
23. The synthesis of fluorinated aromatic compounds can be achieved using aryl fluorides and aryldipalladium catalysts.
24. The stereochemistry of palladium-catalyzed arylation reactions using aryldipalladium catalysts can be controlled by the choice of ligand.
25. The selectivity of arylpalladation reactions using aryldipalladium catalysts can be influenced by the steric demands of the substrate.
26. The use of boronic acids in aryldipalladium catalysis can result in high yields and selectivity.
27. The development of air-stable aryldipalladium catalysts has enabled the use of these compounds in industrial processes.
28. Asymmetric arylation reactions using chiral aryldipalladium catalysts have been shown to be highly selective and efficient.
29. The application of aryldipalladium catalysis to the synthesis of important bioactive molecules has shown great promise.
30. The use of aryl iodides as substrates in aryldipalladium catalysis can lead to formation of products with unique properties.

Common Phases

1. Aryldipalladium-catalyzed cross-coupling reactions allow for efficient carbon-carbon bond formation;
2. The use of aryl iodides as substrates in aryldipalladium-catalyzed reactions is often preferred due to their reactivity;
3. The development of efficient ligands for aryldipalladium catalysts has significantly improved the selectivity and yield of cross-coupling reactions;
4. The stereoselectivity of aryldipalladium-catalyzed cross-coupling reactions can be tuned by altering the structure of the ligands used in the reaction;
5. Aryldipalladium-catalyzed reactions offer a powerful tool for the synthesis of complex organic molecules.

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