ArticleChemSusChem2019
Iron-Catalyzed Borrowing Hydrogen C-Alkylation of Oxindoles with Alcohols.
Article in ChemSusChem, 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.
- Iron-Catalyzed Transfer Hydrogenation of Allylic Alcohols with Isopropanol.The Journal of organic chemistry · 2024Article
- Substituent Effects and Mechanistic Insights on the Catalytic Activities of (Tetraarylcyclopentadienone)iron Carbonyl Compounds in Transfer Hydrogenations and Dehydrogenations.Organometallics · 2023Article
- A nickel phosphide nanoalloy catalyst for the C-3 alkylation of oxindoles with alcohols.Scientific reports · 2021Article
- Borrowing Hydrogen for Organic Synthesis.ACS central science · 2021Review
- A Simple Iron-Catalyst for Alkenylation of Ketones Using Primary Alcohols.Molecules (Basel, Switzerland) · 2020Article
- Cyclopentadienone Iron Tricarbonyl Complexes-Catalyzed Hydrogen Transfer in Water.Molecules (Basel, Switzerland) · 2020Article
- Iron-Catalyzed Acceptorless Dehydrogenative Coupling of Alcohols With Aromatic Diamines: Selective Synthesis of 1,2-Disubstituted Benzimidazoles.Frontiers in chemistry · 2020Article
- One-Pot Conversion of Allylic Alcohols to α-Methyl Ketones via Iron-Catalyzed Isomerization-Methylation.Organic letters · 2019Article
- Iron-Catalyzed Borrowing Hydrogen β-ACS catalysis · 2019Article
- Article
Corrections and comments
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Authors and funding
5 authors.
Funding
Abstract
A general and efficient iron-catalyzed C-alkylation of oxindoles has been developed. This borrowing hydrogen approach employing a (cyclopentadienone)iron carbonyl complex (2 mol %) exhibited a broad reaction scope, allowing benzylic and simple primary and secondary aliphatic alcohols to be employed as alkylating agents. A variety of oxindoles underwent selective mono-C3-alkylation in good-to-excellent isolated yields (28 examples, 50-92 % yield, 79 % average yield).
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Registered trials
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