368427-26-3

Upstream product

• 189228-43-1 (2RS,4R)-2-phenylthiazolidine-4-carboxylic acid ethyl ester 
• 130-15-4 [1,4]naphthoquinone 
• 368427-19-4 (4R) ethyl 2-(4-methylphenyl)thiazolidine-4-carboxylate 
• 78979-47-2 (4R)-ethyl-2-(4-chlorophenyl) thiazolidine-4-carboxylate 
• 78979-49-4 (4R) ethyl 2-(4-nitrophenyl)thiazolidine-4-carboxylate 
• 368427-21-8 (R)-2-(4-Dimethylamino-phenyl)-thiazolidine-4-carboxylic acid ethyl ester 

Downstream Products

• 642471-92-9 3-[N-(tert-butoxycarbonyl)-L-phenylalanyl]amino-3-ethoxycarbonyl-2,3-dihydrothiopheno[2,3-b]naphthalene-4,9-dione 
• 1309667-49-9 3-[(L-phenylalanyl)amino]naphtho[2,3-b]thiophene-4,9-dione trifluoroacetate 
• 642472-08-0 3-(2-amino-3-phenyl-propionylamino)-4,9-dioxo-2,3,4,9-tetrahydro-naphtho[2,3-b]thiophene-3-carboxylic acid ethyl ester 
• 937174-66-8 (3S,3'S)-3-[(N-tritylaminocarbonyl)methyl]spiro[(dihydropyrazine-2,5-dione)-6,3'-(2',3'-dihydrothieno[2,3-b]naphtho-4',9'-dione)] 
• 937174-64-6 (3S,3'R)-3-[(N-tritylaminocarbonyl)methyl]spiro[(dihydropyrazine-2,5-dione)-6,3'-(2',3'-dihydrothieno[2,3-b]naphtho-4',9'-dione)] 
• 937174-58-8 (3S,3'S)-3-[(1-trityl-1H-imidazol-4-yl)methyl]spiro[(dihydropyrazine-2,5-dione)-6,3'-(2',3'-dihydrothieno[2,3-b]naphtho-4',9'-dione)] 
• 937174-56-6 (3S,3'R)-3-[(1-trityl-1H-imidazol-4-yl)methyl]spiro[(dihydropyrazine-2,5-dione)-6,3'-(2',3'-dihydrothieno[2,3-b]naphtho-4',9'-dione)] 
• 937174-50-0 (3R,3'S)-3-[(tritylthio)methyl]spiro[dihydropyrazine-2,5-dione-6,3'-(2',3'-dihydrothieno[2,3-b]naphtho-4',9'-dione)] 
• 937174-48-6 (3R,3'R)-3-[(tritylthio)methyl]spiro[dihydropyrazine-2,5-dione-6,3'-(2',3'-dihydrothieno[2,3-b]naphtho-4',9'-dione)] 
• 937174-42-0 (3S,3'S)-3-[4-(tert-butyloxy)benzyl]spiro[(dihydropyrazine-2,5-dione)-6,3'-(2',3'-dihydrothieno[2,3-b]naphtho-4',9'-dione)] 
• 937174-40-8 (3S,3'R)-3-[4-(tert-butyloxy)benzyl]spiro[(dihydropyrazine-2,5-dione)-6,3'-(2',3'-dihydrothieno[2,3-b]naphtho-4',9'-dione)] 

Relevant academic research and scientific papers

New benzo[g]isoquinoline-5,10-diones and dihydrothieno [2,3-b]naphtho-4,9-dione derivatives: Synthesis and biological evaluation as potential antitumoral agents

Novel antitumoral agents with quinonic structure were synthesized and evaluated for their in vitro cytotoxic activities. This study examines the cytotoxic activities of several aryl benzo[g]isoquinoline-5,10-dione derivatives and a number of aminoacyl dih

Cycloaddition reactions of thiazolidine derivatives. An approach to the synthesis of new functionalized heterocyclic systems

A one-pot procedure for the synthesis of two functionalized tricyclic systems having structures of benzo[g]isoquinoline-5,10-dione and dihydrothieno[2,3-b]naphto-4,9-dione (DTNQ) is described. These new series were synthesized from cycloaddition reactions