2-Hydroxyethyl-Substituted Pd-PEPPSI Complexes: Synthesis, Characterization and the Catalytic Activity in the Suzuki-Miyaura Reaction for Aryl Chlorides in Aqueous Media-Reference-Cited by-同舟云学术

2-Hydroxyethyl-Substituted Pd-PEPPSI Complexes: Synthesis, Characterization and the Catalytic Activity in the Suzuki-Miyaura Reaction for Aryl Chlorides in Aqueous Media

Published:2018-09-17 Issue:35 Volume:3 Page:9974-9980
ISSN:2365-6549
Container-title:ChemistrySelect
language:en
Short-container-title:ChemistrySelect

Author:

Aktaş Aydın¹^ORCID,Celepci Duygu Barut²,Gök Yetkin¹,Aygün Muhittin²

Affiliation:

1. İnönü University; Faculty of Science; Department of Chemistry 44280, Malatya; Turkey

2. Dokuz Eylül University; Faculty of Science; Department of Physics, 35160-Buca, İzmir; Turkey

Publisher

Wiley

Subject

General Chemistry

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/slct.201802046/fullpdf

Reference48 articles.

1. Sterically Encumbered Tetraarylimidazolium Carbene Pd-PEPPSI Complexes: Highly Efficient Direct Arylation of Imidazoles with Aryl Bromides under Aerobic Conditions

2. Palladium catalyzed Mizoroki–Heck and Suzuki–Miyaura reactions using naphthalenomethyl-substituted imidazolidin-2-ylidene ligands in aqueous media

3. Palladium-Catalyzed Cross-Coupling of Silyl Electrophiles with Alkylzinc Halides: A Silyl-Negishi Reaction

4. Sonogashira cross-coupling reaction catalyzed by N-heterocyclic carbene-Pd(II)-PPh3 complexes under copper free and aerobic conditions

5. The Stille Reaction, 38 Years Later

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