Theoretical studies on substrate-controlled selectivity of nickel-catalyzed hydroalkylation of 1,3-dienes-Reference-Cited by-同舟云学术

Theoretical studies on substrate-controlled selectivity of nickel-catalyzed hydroalkylation of 1,3-dienes

Published:2023 Issue:28 Volume:47 Page:13303-13308
ISSN:1144-0546
Container-title:New Journal of Chemistry
language:en
Short-container-title:New J. Chem.

Author:

Liu Yuhua¹^ORCID,Liu Difei²,He Senyu¹,Huang Xiaofeng¹,Ding Feiqing³^ORCID,Zhang Yang⁴

Affiliation:

1. School of Physics and Materials Science, Guangzhou University, Guangzhou, 510006, China

2. College of Chemistry, Jilin Normal University, Siping 136000, P. R. China

3. School of Pharmaceutical Sciences(Shenzhen), Shenzhen Campus of Sun Yat-sen University, Guangzhou, 518107, China

4. Department of Material Science and Engineering, Beijing Technology and Business University, Beijing 100048, China

Abstract

The detailed mechanism of the substrate-controlled selectivity in the nickel-catalyzed hydroalkylation of 2-substituted 1,3-diene has been investigated.

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,General Chemistry,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2023/NJ/D3NJ01776A

Reference45 articles.

1. Synergizing palladium with Lewis base catalysis for stereodivergent coupling of 1,3-dienes with pentafluorophenyl acetates

2. Ni-Catalyzed Enantioselective Hydrofunctionalizations of 1,3-Dienes

3. Directing Group‐Promoted Inert C−O Bond Activation Using Versatile Boronic Acid as a Coupling Agent

4. Effective fabrication of flexible nickel chains/acrylate composite pressure-sensitive adhesives with layered structure for tunable electromagnetic interference shielding

5. 3D porous nickel metal foam/polyaniline heterostructure with excellent electromagnetic interference shielding capability and superior absorption based on pre-constructed macroscopic conductive framework