Complications in the Castagnoli-Cushman reaction: An unusual course of reaction between cyclic anhydrides and sterically hindered indolenines
Author:
Funder
Russian Scientific Fund
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference19 articles.
1. Condensation of succinic anhydride with N-benzylidene-N-methylamine. Stereoselective synthesis of trans- and cis-1-methyl-4-carboxy-5-phenyl-2-pyrrolidinone
2. Condensation of succinic anhydrides with Schiff bases. Scope and mechanism
3. Current diversity of cyclic anhydrides for the Castagnoli–Cushman-type formal cycloaddition reactions: prospects and challenges
4. Convenient modular construction of medicinally important 5-acylamino-4,5-dihydroisoxazoles featuring four elements of diversity
5. Microwave-promoted reaction of N-(alk-1-enyl)chloroacetamides with sodium azide unexpectedly yields 1H-imidazol-5(4H)-ones
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1. The Castagnoli–Cushman Reaction;Molecules;2023-03-15
2. Novel angularly substituted [1,4]thiazino[3,4‐a]isoquinoline carboxylic acids prepared by cyclic imine‐cyclic anhydride reaction;Journal of Heterocyclic Chemistry;2022-12-08
3. Mechanistic Investigation of Castagnoli–Cushman Multicomponent Reactions Leading to a Three-Component Synthesis of Dihydroisoquinolones;The Journal of Organic Chemistry;2021-08-05
4. One-step route to tricyclic fused 1,2,3,4-tetrahydroisoquinoline systems via the Castagnoli–Cushman protocol;Beilstein Journal of Organic Chemistry;2020-06-24
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