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Facile Three-Component Reactions for the Synthesis of N-Unsubstituted 1h‑Pyrrol-3(2h)‑Ones and Base Induced Divergent N-H and C-C Bond Functionalizations
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Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/anie.202014796openalex-extracted
Palladium‐Catalyzed Enantioselective Heteroarenyne Cycloisomerization Reaction
inferredcites →https://doi.org/10.1016/0040-4039(94)88306-8openalex-extracted
An efficient and mild synthesis of highly substituted imidazoles
inferredcites →https://doi.org/10.1016/s0040-4039(00)79459-7openalex-extracted
Benzilic acid rearrangements in the reactions of aryl vicinal tricarbonyl derivatives with aldehyde schiff bases
inferredcites →https://doi.org/10.1021/acs.joc.1c02753openalex-extracted
Synthetic Studies toward 1,2,3,3a,4,8b-Hexahydropyrrolo[3,2-b]indole Core. Unusual Fragmentation with 1,2-Aryl Shift
inferredcites →https://doi.org/10.1021/acs.joc.8b01887openalex-extracted
Synthesis of 1H-Pyrrol-3(2H)-ones via Three-Component Reactions of 2,3-Diketo Esters, Amines, and Ketones
inferredcites →https://doi.org/10.1021/acs.orglett.1c00827openalex-extracted
Delocalization Effects and Tunable Emission in a Class of Charged Cyclazines with Nitrogen on the Periphery
inferredcites →https://doi.org/10.1021/jo0355350openalex-extracted
Oxidation of Indole Substrates by Oxodiperoxomolybdenum·Trialkyl(aryl)- phosphine Oxide Complexes
inferredcites →https://doi.org/10.1038/s41557-020-0442-3openalex-extracted
Total synthesis of brevianamide A
inferredcites →https://doi.org/10.1039/c5cc07780jopenalex-extracted
Asymmetric synthesis of 1H-pyrrol-3(2H)-ones from 2,3-diketoesters by combination of aldol condensation with benzilic acid rearrangement
inferredcites →https://doi.org/10.1039/c7cc03754fopenalex-extracted
Facile access to 2,2-disubstituted indolin-3-ones via a cascade Fischer indolization/Claisen rearrangement reaction
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