Phthalide: a direct building-block towards P,O and P,N hemilabile ligands. Application in the palladium-catalysed Suzuki–Miyaura cross-coupling of aryl chlorides-Reference-Cited by-同舟云学术

Phthalide: a direct building-block towards P,O and P,N hemilabile ligands. Application in the palladium-catalysed Suzuki–Miyaura cross-coupling of aryl chlorides

Published:2013 Issue:15 Volume:11 Page:2404
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

McNulty James,Keskar Kunal

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2013/OB/C3OB40198G

Reference63 articles.

1. Hemilability of Hybrid Ligands and the Coordination Chemistry of Oxazoline-Based Systems

2. Metal Unsaturation and Ligand Hemilability in Suzuki Coupling

3. Palladium/P,O-Ligand-Catalyzed Suzuki Cross-Coupling Reactions of Arylboronic Acids and Aryl Chlorides. Isolation and Structural Characterization of (P,O)-Pd(dba) Complex

4. A New Family of Tunable Indolylphosphine Ligands by One-Pot Assembly and Their Applications in Suzuki−Miyaura Coupling of Aryl Chlorides

5. Suzuki−Miyaura Coupling of Aryl Tosylates Catalyzed by an Array of Indolyl Phosphine−Palladium Catalysts

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1. Acid–base-sensitive allylic oxidation of 2-allylbenzoic acids to form phthalides;Organic & Biomolecular Chemistry;2020

2. Suzuki-Miyaura cross-coupling reaction of aryl chlorides with aryl boronic acids catalyzed by a palladium dichloride adduct of N-diphenylphosphanyl-2-aminopyridine;Tetrahedron;2017-06

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4. Palladium complex containing two sterically hindered ligands as highly efficient catalyst for Suzuki-Miyaura reaction;Applied Organometallic Chemistry;2015-09-22

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