A novel asymmetric nickel-based procedure has been developed in which CO fixation is achieved as a second step of a truncated Heck coupling. For this, a new chiral ligand has been prepared and shown to achieve enantiomeric excesses up to 99 %. The overall process efficiently furnishes chiral 2,3-dihydrobenzofuran-3-ylacetic acids, an important class of bioactive products, from easy to prepare starting materials. A combined experimental and computational effort revealed the key steps of the catalytic cycle and suggested the unexpected participation of Ni(I) species in the coupling event.

Download full-text PDF

Source
http://dx.doi.org/10.1002/chem.202101082DOI Listing

Publication Analysis

Top Keywords

enantioselective fixation
4
fixation heck-coupling/carboxylation
4
heck-coupling/carboxylation cascade
4
cascade catalyzed
4
catalyzed nickel
4
nickel novel
4
novel asymmetric
4
asymmetric nickel-based
4
nickel-based procedure
4
procedure developed
4

Similar Publications

Enzymatic Cascades for Stereoselective and Regioselective Amide Bond Assembly.

Angew Chem Int Ed Engl

January 2025

The University of Manchester, School of Chemistry & Manchester Institute of Biotechnology, 131 Princess Street, M1 7DN, Manchester, UNITED KINGDOM OF GREAT BRITAIN AND NORTHERN IRELAND.

Amide bond formation is fundamental in nature and is widely used in the synthesis of pharmaceuticals and other valuable products. Current methods for amide synthesis are often step and atom inefficient, requiring the use of protecting groups, deleterious reagents and organic solvents that create significant waste. The development of cleaner and more efficient catalytic methods for amide synthesis remains an urgent unmet need.

View Article and Find Full Text PDF

Multifunctional Magnetic Chiral HKUST MOF Decorated by Triazine, FeO, and Cu(l-Proline) Complex for Green and Mild Asymmetric Catalysis.

ACS Appl Mater Interfaces

December 2024

Department of Chemistry, Faculty of Sciences, Tarbiat Modares University, 14117-13116 Tehran, Islamic Republic of Iran.

A multifunctional magnetic chiral metal-organic framework (MOF) was developed for asymmetric applications by utilizing strategies of chiralization and multifunctionalization. Cu(l-proline)-Triazine/FeO@SiO-NH was employed as a chiral secondary agent to synthesize a chiral hybrid nanocomposite within a MOF. The use of a chiral secondary agent efficiently induces chirality in an achiral MOF structure that cannot be directly chiralized.

View Article and Find Full Text PDF

Enantioselective Nickel-Electrocatalyzed Reductive Propargylic Carboxylation with CO.

J Am Chem Soc

May 2024

Hefei National Research Center for Physical Sciences at the Microscale and Department of Chemistry, University of Science and Technology of China, Hefei 230026, China.

Article Synopsis
  • The text discusses the use of carbon dioxide (CO) as a sustainable source for creating specific carboxylic acids through a new electrochemical reaction.
  • A nickel catalyst is employed to efficiently facilitate this process without needing moisture-sensitive chemicals, allowing for the formation of carbon-carbon (C-C) bonds.
  • This method has shown high efficacy, reaching up to 98% in terms of the purity of the desired product, and has been applied in the total synthesis of various complex organic molecules, highlighting its potential in sustainable chemistry.
View Article and Find Full Text PDF

α,α-Disubstituted α-amino acids (α-AAs) have improved properties compared to other types of amino acids. They serve as modifiers of peptide conformation and as precursors of bioactive compounds. Therefore, it has been a long-standing goal to construct this highly valuable scaffold efficiently in organic synthesis and drug discovery.

View Article and Find Full Text PDF

Chiral pesticides are unique hazardous materials. Here, we systematically studied the potentially harmful products of enantioselective indoxacarb degradation throughout tea growth, processing, and brewing and tested their toxicity to tea geometrid larvae and honeybees. The half-lives of S-indoxacarb and R-indoxacarb during tea growth were 2.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!