Oxidative rearrangement of 2-(2-aminobenzyl) furans affording 2-(2-acylvinyl) indoles in a
stereocontrolled manner in good-to-excellent yields has been developed. Thus,(2 …

The acid-catalyzed rearrangement of 5-alkyl-2-[2-(sulfonylamino) phenyl] furans into 2-(2-
oxoalkyl) indoles is described. When the N-sulfonyl group in the starting compounds was …

A short, efficient and novel approach for the syntheses of bis‐indole alkaloids flinderoles A−
C, and desmethylflinderole C, is being described. The synthesis utilizes the optimized …

Furan as a 1,3-diketone equivalent: the second type furan recyclization applied to indole
synthesis - ScienceDirect Skip to main contentSkip to article Elsevier logo Journals & Books …

A new approach to the synthesis of 4-(2-indolyl)-3-buten-2-ones is described based on
condensation of 2-tosylaminobenzyl alcohols with N-tosylfurfurylamine. Pseudooxidative …

The regioselective hydroxyalkylation of 4, 5, 6, 7-tetrahydroindole at position 2 using highly
electrophilic polyfluorocarbonyl compounds was performed for the first time. Oxidation of the …

A facile synthesis of 6-hydroxyindole and 6-methoxyindole starting from indole is described.
Regioselective chloroacetylation of 1-pivaloylindole followed by Baeyer-Villiger oxidation …

An auto oxidation‐rearrangement product 4 was isolated from a high dilution reaction of
ninhydrin with 3, 4, 5‐trimethoxyaniline in water. A general synthesis of this compound and …

A concise synthesis of 3-hydroxyindole-2-carboxylates by a modified Baeyer–Villiger
oxidation - ScienceDirect Skip to main contentSkip to article Elsevier logo Journals & Books …

A new methodology for the synthesis of indole and benzofuran derivatives has been
devised. The starting materials, ortho-substituted aryl diynes, have been easily converted …