Arylation of chloroanthraquinones by surprisingly facile Suzuki–Miyaura cross-coupling reactions-Reference-Cited by-同舟云学术

Arylation of chloroanthraquinones by surprisingly facile Suzuki–Miyaura cross-coupling reactions

Published:2009-12 Issue:12 Volume:2009 Page:732-736
ISSN:1747-5198
Container-title:Journal of Chemical Research
language:en
Short-container-title:Journal of Chemical Research

Author:

Thiemann Thies¹²,Tanaka Yasuko³,Iniesta Jesus⁴,Varghese H. Tresa⁵,Pannicker C. Yohannan⁶

Affiliation:

1. Interdisciplinary Graduate School of Engineering Sciences and

2. Department of Chemistry, Faculty of Science, United Arab Emirates University, PO Box 17551, Al Ain, United Arab Emirates.

3. Institute of Materials Chemistry and Engineering, Kyushu University, 6–1, Kasuga-koh-en, Kasuga-shi, Fukuoka 816-8580, Japan

4. Department of Physical Chemistry, University of Alicante, E-03080 Alicante, Spain

5. Department of Physics, Fatima Mata National College, Kollam-1, India

6. Department of Physics, TKM College of Arts and Science, Kollam-5, Kerala, India

Abstract

Chloroanthraquinones were found to undergo facile Suzuki–cross coupling with substituted phenyl boronic acids using a commercial catalyst Pd(PPh3)4 and with Pd(PPh3)4 prepared in situ from Pd(PPh3)2Cl2 and PPh3.

Publisher

SAGE Publications

Subject

General Chemistry

Link

http://journals.sagepub.com/doi/pdf/10.3184/030823409X12586584303880

Reference31 articles.

1. New applications of organometallic catalysts in organic chemistry

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3. Palladium-bisimidazol-2-ylidene complexes as catalysts for general and efficient Suzuki cross-coupling reactions of aryl chlorides with arylboronic acids

4. Palladium−Imidazol-2-ylidene Complexes as Catalysts for Facile and Efficient Suzuki Cross-Coupling Reactions of Aryl Chlorides with Arylboronic Acids

5. Molecularly defined palladium(0) monophosphine complexes as catalysts for efficient cross-coupling of aryl chlorides and phenylboronic acid1

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