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Triphenylphosphine chalcogenides as efficient ligands for room temperature palladium(II)-catalyzed Suzuki–Miyaura reaction

✍ Scribed by Pankaj Das; Utpal Bora; Archana Tairai; Chandan Sharma

Book ID
104097368
Publisher
Elsevier Science
Year
2010
Tongue
French
Weight
275 KB
Volume
51
Category
Article
ISSN
0040-4039

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✦ Synopsis

A simple catalytic system based on PdCl 2 and triphenylphosphine chalcogenides (PPh 3 X; X = O, S, Se) is found to be highly effective (up to 97% isolated yield) in the room temperature Suzuki-Miyaura reactions. Under the same experimental conditions, triphenylphosphine chalcogenides as ligands show superior activities compared to free triphenylphosphine.

📜 SIMILAR VOLUMES

ChemInform Abstract: Triphenylphosphine
ChemInform Abstract: Triphenylphosphine Chalcogenides as Efficient Ligands for Room Temperature Palladium(II)-Catalyzed Suzuki—Miyaura Reaction.
✍ Pankaj Das; Utpal Bora; Archana Tairai; Chandan Sharma 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 25 KB 👁 1 views

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