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Oxidative [3+3] Annulation of Atropaldehyde Acetals with 1,3‐Bisnucleophiles: An Efficient Method of Constructing Six‐Membered Aromatic Rings, Including Salicylates and Carbazoles

https://doi.org/10.1002/adsc.201800462

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Outgoing claims: the papers this work cites, builds on, or argues with.

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inferred← citeshttps://doi.org/10.1021/acs.joc.5c03226openalex-snapshot

Conversion of Diverse Aromatic Amines to 3-Acyl-Substituted Pyridine/Pyrimidine-Fused Heterocyclic Derivatives via the Combination of Rongalite and Enaminones

inferred← citeshttps://doi.org/10.1021/acs.joc.9b00270openalex-snapshot

Lewis Acid-Catalyzed Synthesis of Benzofurans and 4,5,6,7-Tetrahydrobenzofurans from Acrolein Dimer and 1,3-Dicarbonyl Compounds

inferred← citeshttps://doi.org/10.1021/acs.joc.9b00334openalex-snapshot

Selectivity in the Photo-Fries Rearrangement of Some Aryl Benzoates in Green and Sustainable Media. Preparative and Mechanistic Studies

inferred← citeshttps://doi.org/10.1021/acs.orglett.5c04445openalex-snapshot

Nickel-Catalyzed Quinoline Synthesis through Skeletal Editing Strategy Using Calcium Carbide as an Inorganic C2 Source

inferred← citeshttps://doi.org/10.1021/acs.orglett.8b02898openalex-snapshot

Recycling Catalyst as Reactant: A Sustainable Strategy To Improve Atom Efficiency of Organocatalytic Tandem Reactions

inferred← citeshttps://doi.org/10.1039/c8gc04000aopenalex-snapshot

Utilization of bio-based glycolaldehyde aqueous solution in organic synthesis: application to the synthesis of 2,3-dihydrofurans

inferred← citeshttps://doi.org/10.1039/d1cc04000fopenalex-snapshot

Acid-catalyzed cleavage of C–C bonds enables atropaldehyde acetals as masked C2 electrophiles for organic synthesis

inferred← citeshttps://doi.org/10.1039/d1ra04372bopenalex-snapshot

Indoleninyl-substituted pyrimido[1,2- b ]indazoles via a facile condensation reaction

inferred← citeshttps://doi.org/10.3389/fchem.2020.00466openalex-snapshot

I2/DMSO-Catalyzed Transformation of N-tosylhydrazones to 1,2,3-thiadiazoles

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