A facile approach to ketones via Pd-catalyzed sequential carbonylation of olefins with formic acid
Author:
Affiliation:
1. State Key Laboratory of Coordination Chemistry
2. Collaborative Innovation Center of Chemistry for Life Sciences
3. Center for Multimolecular Organic Chemistry
4. School of Chemistry and Chemical Engineering
5. Nanjing University
Abstract
An effective palladium-catalyzed sequential carbonylation of olefins with formic acid is described.
Funder
National Natural Science Foundation of China
Publisher
Royal Society of Chemistry (RSC)
Subject
Organic Chemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2017/QO/C7QO00111H
Reference51 articles.
1. Palladium-Catalyzed Reppe Carbonylation
2. Pd-catalysed asymmetric mono- and bis-alkoxycarbonylation of vinylarenes
3. Palladium-Catalyzed Carbonylation Reactions of Alkenes and Alkynes
4. Cationic palladium(II)–diphosphine complexes as catalysts for the carbonylation of alkenes to ketones
5. Selectivity of the carbonylation of styrene by cationic palladium complexes
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1. Pd-Catalyzed Regioselective Hydroformylation of Olefins with HCO2H and Its Derivatives;Organic Letters;2023-09-27
2. Formic Acid as an Inexpensive and Convenient Reagent;Current Organic Chemistry;2021-02-04
3. Carbonylative cycloaddition between two different alkenes enabled by reactive directing groups: expedited construction of bridged polycyclic skeletons;Chemical Communications;2020
4. Conversion of Formic Acid in Organic Synthesis as a C1 Source;Springer Theses;2020
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