128233-26-1

Upstream product

• 762-21-0 acetylenedicarboxylic acid diethyl ester 
• 911808-80-5 C₁₅H₁₉NO₅ 
• 90-04-0 2-methoxy-phenylamine 

Downstream Products

• 1421606-53-2 ethyl 4-(benzyloxy)-8-methoxyquinoline-2-carboxylate 
• 1421606-59-8 4-(benzyloxy)-8-methoxyquinoline-2-carboxamide 
• 1421606-62-3 (E)-4,8-dimethoxy-N-(4-methoxystyryl)quinoline-2-carboxamide 
• 1421606-63-4 (E)-N-(4-(benzyloxy)styryl)-4,8-dimethoxyquinoline-2-carboxamide 
• 1421606-64-5 (E)-4,8-dimethoxy-N-(2,5-dimethoxystyryl)quinoline-2-carboxamide 
• 1421606-65-6 (E)-4,8-dimethoxy-N-(3,4,5-trimethoxystyryl)quinoline-2-carboxamide 
• 1421606-73-6 (E)-4-(benzyloxy)-N-(4-(benzyloxy)styryl)-8-methoxyquinoline-2-carboxamide 
• 1421606-74-7 (E)-4-(benzyloxy)-8-methoxy-N-(4-methoxystyryl)quinoline-2-carboxamide 
• 1421606-76-9 (E)-4-ethoxy-8-methoxy-N-(4-(methylthio)styryl)quinoline-2-carboxamide 
• 1421606-77-0 (E)-4-ethoxy-8-methoxy-N-(4-methoxystyryl)quinoline-2-carboxamide 

Relevant academic research and scientific papers

Synthesis of perspicamide A and related diverse analogues: Their bioevaluation as potent antileishmanial agents

The first protocol for the synthesis of perspicamide A and related diverse analogues has been developed from economical and readily available starting materials. Furthermore, a few synthesized analogues, 24a, 24b, 24c, 24d, and 24l, exhibited potent activ

Process for preparing certain pyrano[3,2-g]quinoline 2,8-dicarboxylates and 4-oxo-quinoline-2-carboxylates

There is described a process for the production of a 1,4-dihydro-4-oxo-quinoline-2-carboxylic acid, or a salt, ester or amide thereof, which comprises cyclization of a corresponding 2-aminobenzoyl pyruvic acid or an ester thereof, and if desired or necess