ArticleChemical science2019
Highly-chemoselective step-down reduction of carboxylic acids to aromatic hydrocarbons
Article in Chemical science, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.
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Who cites it
10 citing papers in PubMed.
- Metal-free highly chemo-selective bisphosphorylation and deoxyphosphorylation of carboxylic acids.Chemical science · 2023Article
- Nickel-catalyzed reductive decarboxylation of fatty acids for drop-in biofuel production.RSC advances · 2022Article
- PdAngewandte Chemie (International ed. in English) · 2022Article
- Decarbonylative Pd-Catalyzed Suzuki Cross-Coupling for the Synthesis of Structurally Diverse Heterobiaryls.Organic letters · 2022Article
- Decarbonylative Sonogashira Cross-Coupling: Fruitful Marriage of Alkynes with Carboxylic Acid Electrophiles.Organic chemistry frontiers : an international journal of organic chemistry · 2022Article
- Decarbonylative Sulfide Synthesis from Carboxylic Acids and Thioesters via Cross-Over C-S Activation and Acyl Capture.Organic chemistry frontiers : an international journal of organic chemistry · 2021Article
- Decarbonylative Sonogashira Cross-Coupling of Carboxylic Acids.Organic letters · 2021Article
- Bimetallic Cooperative Catalysis for Decarbonylative Heteroarylation of Carboxylic Acids via C-O/C-H Coupling.Angewandte Chemie (International ed. in English) · 2021Article
- Decarbonylative Suzuki-Miyaura Cross-Coupling of Aroyl Chlorides.Organic letters · 2020Article
- Synthesis of Biaryls via Decarbonylative Palladium-Catalyzed Suzuki-Miyaura Cross-Coupling of Carboxylic Acids.iScience · 2019Article
Corrections and comments
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Authors and funding
5 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Aryl carboxylic acids are among the most abundant substrates in chemical synthesis and represent a perfect example of a traceless directing group that is central to many processes in the preparation of pharmaceuticals, natural products and polymers. Herein, we describe a highly selective method for the direct step-down reduction of carboxylic acids to arenes, proceeding
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.