ReviewBeilstein journal of organic chemistry2017
Transition-metal-catalyzed synthesis of phenols and aryl thiols.
Review in Beilstein journal of organic chemistry, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.
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Who cites it
8 citing papers in PubMed, 44 citations in OpenAlex.
- Direct C-H Hydroxylation ofJournal of the American Chemical Society · 2024Article
- Direct conversion of carboxylic acids to free thiolsChemical science · 2024Article
- Ligand-Enabled C-H Hydroxylation with Aqueous HJournal of the American Chemical Society · 2022Article
- Catalytic synthesis of phenols with nitrous oxide.Nature · 2022Article
- Selective hydroxylation of aryl iodides to produce phenols under mild conditions using a supported copper catalyst.RSC advances · 2021Article
- Novel library synthesis of 3,4-disubstituted pyridin-2(1Beilstein journal of organic chemistry · 2021Article
- Metal-free C-H mercaptalization of benzothiazoles and benzoxazoles using 1,3-propanedithiol as thiol source.Beilstein journal of organic chemistry · 2019Article
- Investigations on Gold-Catalyzed Thioalkyne Activation Toward Facile Synthesis of Ketene Dithioacetals.Chemistry (Weinheim an der Bergstrasse, Germany) · 2017Article
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Authors and funding
3 authors at 2 institutions in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Phenols and aryl thiols are fundamental building blocks in organic synthesis and final products with interesting biological activities. Over the past decades, substantial progress has been made in transition-metal-catalyzed coupling reactions, which resulted in the emergence of new methods for the synthesis of phenols and aryl thiols. Aryl halides have been extensively studied as substrates for the synthesis of phenols and aryl thiols. In very recent years, C-H activation represents a powerful strategy for the construction of functionalized phenols directly from various arenes. However, the synthesis of aryl thiols through C-H activation has not been reported. In this review, a brief overview is given of the recent advances in synthetic strategies for both phenols and aryl thiols.
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