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Literature DB >> 26305994

Nanonickel-catalyzed Suzuki-Miyaura cross-couplings in water.

Sachin Handa¹, Eric D Slack¹, Bruce H Lipshutz².

Abstract

Nickel nanoparticles, formed in situ and used in combination with micellar catalysis, catalyze Suzuki-Miyaura cross-couplings in water under very mild reaction conditions.

Entities: Chemical Disease Gene

Keywords: cross-couplings; green chemistry; micelles; nanoparticles; nickel

Mesh：

Substances：

Year: 2015 PMID： 26305994 PMCID： PMC4677689 DOI： 10.1002/anie.201505136

Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN： 1433-7851 Impact factor: 15.336

18 in total

1. Palladium-catalyzed cross-coupling: a historical contextual perspective to the 2010 Nobel Prize.

Authors: Carin C C Johansson Seechurn; Matthew O Kitching; Thomas J Colacot; Victor Snieckus
Journal: Angew Chem Int Ed Engl Date: 2012-05-09 Impact factor: 15.336

Review 2. Advances in transition metal (Pd, Ni, Fe)-catalyzed cross-coupling reactions using alkyl-organometallics as reaction partners.

Authors: Ranjan Jana; Tejas P Pathak; Matthew S Sigman
Journal: Chem Rev Date: 2011-02-14 Impact factor: 60.622

3. Arylation of α-pivaloxyl ketones with arylboronic reagents via Ni-catalyzed sp3 C-O activation.

Authors: Kun Huang; Gang Li; Wei-Ping Huang; Da-Gang Yu; Zhang-Jie Shi
Journal: Chem Commun (Camb) Date: 2011-05-27 Impact factor: 6.222

4. Suzuki-Miyaura cross-coupling of aryl carbamates and sulfamates: experimental and computational studies.

Authors: Kyle W Quasdorf; Aurora Antoft-Finch; Peng Liu; Amanda L Silberstein; Anna Komaromi; Tom Blackburn; Stephen D Ramgren; K N Houk; Victor Snieckus; Neil K Garg
Journal: J Am Chem Soc Date: 2011-04-01 Impact factor: 15.419

5. Synthesis of Biaryls via a Nickel(0)-Catalyzed Cross-Coupling Reaction of Chloroarenes with Arylboronic Acids.

Authors: Syun Saito; Saori Oh-Tani; Norio Miyaura
Journal: J Org Chem Date: 1997-11-14 Impact factor: 4.354

6. Development of an air-stable nickel precatalyst for the amination of aryl chlorides, sulfamates, mesylates, and triflates.

Authors: Nathaniel H Park; Georgiy Teverovskiy; Stephen L Buchwald
Journal: Org Lett Date: 2013-11-27 Impact factor: 6.005

7. NiCl(2)(dppe)-catalyzed cross-coupling of aryl mesylates, arenesulfonates, and halides with arylboronic acids.

Authors: Virgil Percec; Geoffrey M Golding; Jan Smidrkal; Oliver Weichold
Journal: J Org Chem Date: 2004-05-14 Impact factor: 4.354

8. Transition-metal-catalyzed Suzuki-Miyaura cross-coupling reactions: a remarkable advance from palladium to nickel catalysts.

Authors: Fu-She Han
Journal: Chem Soc Rev Date: 2013-06-21 Impact factor: 54.564

Review 9. Recent advances in homogeneous nickel catalysis.

Authors: Sarah Z Tasker; Eric A Standley; Timothy F Jamison
Journal: Nature Date: 2014-05-15 Impact factor: 49.962

10. Transforming Suzuki-Miyaura cross-couplings of MIDA boronates into a green technology: no organic solvents.

Authors: Nicholas A Isley; Fabrice Gallou; Bruce H Lipshutz
Journal: J Am Chem Soc Date: 2013-11-13 Impact factor: 15.419

5 in total

1. Computational Approach to Molecular Catalysis by 3d Transition Metals: Challenges and Opportunities.

Authors: Konstantinos D Vogiatzis; Mikhail V Polynski; Justin K Kirkland; Jacob Townsend; Ali Hashemi; Chong Liu; Evgeny A Pidko
Journal: Chem Rev Date: 2018-10-30 Impact factor: 60.622

2. HandaPhos: A General Ligand Enabling Sustainable ppm Levels of Palladium-Catalyzed Cross-Couplings in Water at Room Temperature.

Authors: Sachin Handa; Martin P Andersson; Fabrice Gallou; John Reilly; Bruce H Lipshutz
Journal: Angew Chem Int Ed Engl Date: 2016-02-29 Impact factor: 15.336