2-Alkylindoles via palladium-catalyzed reductive cyclization of ethyl 3-(o-trifluoroacetamidophenyl)-1-propargyl carbonates
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference38 articles.
1. Synthesis and Functionalization of Indoles Through Palladium-catalyzed Reactions
2. Practical Methodologies for the Synthesis of Indoles
3. 2,3-Disubstituted Indoles through the Palladium-Catalyzed Reaction of Aryl Chlorides witho-Alkynyltrifluoroacetanilides
4. Palladium-Catalyzed Synthesis of 2-(Aminomethyl)indoles from Ethyl 3-(o-Trifluoroacetamidophenyl)-1-propargyl Carbonate
5. Carbon dioxide: a reagent for simultaneous protection of nucleophilic centers and the activation of alternative locations to electrophilic attack. V. Activation of the 2-alkyl group of a 2-alkylindole toward proton loss and subsequent electrophilic substitution
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1. Recent Advances in Indole Synthesis and the Related Alkylation;Asian Journal of Organic Chemistry;2023-05-12
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3. Applications of palladium dibenzylideneacetone as catalyst in the synthesis of five-membered N-heterocycles;Synthetic Communications;2018-12-22
4. Palladium-Acid Co-Catalyzed Cleavage of Alkynoates to Construct Dibenzo[c,h]xanthene Derivatives;Advanced Synthesis & Catalysis;2018-09-04
5. 2-(Aminomethyl)-3-arylindoles from 3-(o-Trifluoroacetamidoaryl)-1-propargylic Alcohols, Aryl Halides, and Amines: A Domino Palladium-Catalyzed Three-Component Approach;Synthesis;2017-04-28
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