896161-14-1

Upstream product

• 18358-63-9 methyl 4-(N-methyl)aminobenzoate 
• 19718-49-1 4-amino-3-iodobenzoic acid methyl ester 
• 67-56-1 methanol 
• 72451-22-0 5-bromo-1,3,3-trimethyl-1,3-dihydro-2H-indol-2-one 
• 201230-82-2 carbon monoxide 

Downstream Products

• 1383541-97-6 C₂₃H₂₂ClN₃O₂ 
• 896160-47-7 1,3,3trimethyl-2,3-dihydro-2-oxo-(1H)-5-indole-carboxylic acid 

Relevant academic research and scientific papers

Visible-Light-Induced Palladium-Catalyzed Generation of Aryl Radicals from Aryl Triflates

A mild visible-light-induced Pd-catalyzed intramolecular C?H arylation of amides is reported. The method operates by cleavage of a C(sp2)?O bond, leading to hybrid aryl Pd-radical intermediates. The following 1,5-hydrogen atom translocation, intramolecular cyclization, and rearomatization steps lead to valuable oxindole and isoindoline-1-one motifs. Notably, this method provides access to products with readily enolizable functional groups that are incompatible with traditional Pd-catalyzed conditions.

Intramolecular 1,5-H transfer reaction of aryl iodides through visible-light photoredox catalysis: A concise method for the synthesis of natural product scaffolds

The intramolecular 1,5-H transfer reaction of the aryl radicals generated from unactivated aryl iodides by photocatalysis is described. The features of this transformation are operational simplicity, excellent yields, mild reaction conditions, and good fu

NOVEL ANTIFUNGAL 5,6-DIHYDRO-4H-PYRROLO[1,2-a][1,4]- BENZODIAZEPINES AND 6H-PYRROLO[1,2-a][1,4]BENZODIAZEPINES SUBSTITUTED WITH BICYCLIC BENZENE DERIVATIVES

The present invention is concerned with novel antifungal 5,6-dihydro-4H-pyrrolo- [1,2-a][1,4]benzodiazepines and 6H-pyrrolo[1,2-a][1,4]benzodiazepines substituted with bicyclic benzene derivatives of Formula (I) wherein R1, R2, Rsup