Regioselective hydroesterification of alkenes and alkenylphenols utilizing CO<sub>2</sub> and hydrosilane-Reference-Cited by-同舟云学术

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Regioselective hydroesterification of alkenes and alkenylphenols utilizing CO₂ and hydrosilane

Published:2023 Issue:20 Volume:14 Page:5483-5489
ISSN:2041-6520
Container-title:Chemical Science
language:en
Short-container-title:Chem. Sci.

Author:

Wang Meng-Meng¹²,Lu Sheng-Mei¹,Li Can¹²^ORCID

Affiliation:

1. State Key Laboratory of Catalysis, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian National Laboratory for Clean Energy, Dalian 116023, China

2. University of Chinese Academy of Sciences, Beijing 100049, China

Abstract

Regioselective hydroesterification of alkenes and alkenylphenols was achieved utilizing CO2 as a CO source with the assistance of PMHS.

Funder

National Natural Science Foundation of China

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2023/SC/D3SC01114C

Reference59 articles.

1. Palladium-Catalyzed Reppe Carbonylation

2. State-of-the-art palladium-catalyzed alkoxycarbonylations

3. Catalytic Asymmetric Cyclocarbonylation of o-Isopropenylphenols: Enantioselective Synthesis of Six-Membered Ring Lactones

4. Recyclable Selective Palladium-Catalyzed Synthesis of Five-, Six- or Seven-Membered Ring Lactones and Lactams by Cyclocarbonylation in Ionic Liquids

5. Highly selective formation of linear esters from terminal and internal alkenes catalysed by palladium complexes of bis-(di-tert-butylphosphinomethyl)benzene

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