Pd-Catalyzed Suzuki coupling reactions of aryl halides containing basic nitrogen centers with arylboronic acids in water in the absence of added base-Reference-Cited by-同舟云学术

Pd-Catalyzed Suzuki coupling reactions of aryl halides containing basic nitrogen centers with arylboronic acids in water in the absence of added base

Published:2017 Issue:24 Volume:41 Page:15420-15432
ISSN:1144-0546
Container-title:New Journal of Chemistry
language:en
Short-container-title:New J. Chem.

Author:

Li Zhao¹²³⁴^ORCID,Gelbaum Carol¹²³⁴,Campbell Zachary S.⁵²³⁴,Gould Paul C.¹²³⁴,Fisk Jason S.⁶⁷⁴,Holden Bruce⁶⁷⁴,Jaganathan Arvind⁸⁹¹⁰⁴,Whiteker Gregory T.⁸⁹¹⁰⁴,Pollet Pamela¹²³⁴,Liotta Charles L.¹²³⁴⁵

Affiliation:

1. School of Chemistry and Biochemistry

2. Georgia Institute of Technology

3. Atlanta

4. USA

5. School of Chemical and Biomolecular Engineering

6. The Dow Chemical Company

7. Midland

8. Dow AgroSciences

9. Indianapolis

10. Indiana 46268

Abstract

Successful Suzuki reactions of basic nitrogen containing aryl chlorides/bromides with arylboronic acids in water without added base, partially or entirely under acidic conditions.

Funder

Dow Chemical Company

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,General Chemistry,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2017/NJ/C7NJ03567E

Reference70 articles.

1. Stereoselective synthesis of arylated (E)-alkenes by the reaction of alk-1-enylboranes with aryl halides in the presence of palladium catalyst

2. A new stereospecific cross-coupling by the palladium-catalyzed reaction of 1-alkenylboranes with 1-alkenyl or 1-alkynyl halides

3. Palladium-Catalyzed Cross-Coupling Reactions of Organoboron Compounds