161265-32-3

Usage

Synthesis Reference(s)

Tetrahedron Letters, 36, p. 125, 1995 DOI: 10.1016/0040-4039(94)02191-D

Upstream product

• 59586-11-7 3-(trichlorostannyl)propanoic acid 
• 618-51-9 3-Iodobenzoic acid 
• 25974-99-6 3-(2-carboxyvinyl)benzoic acid 
• 124-38-9 carbon dioxide 
• 10601-99-7 3-ethynylbenzoic acid 
• 619-21-6 m-formylphenyl benzoic acid 
• 10036-18-7 <3-Ethoxycarbonyl-benzyl>-malonsaeure-diethylester 
• 115974-98-6 3-[(E)-2-carboxyvinyl]-benzoic acid 

Downstream Products

• 10036-21-2 3-(3-(ethoxycarbonyl)phenyl)propanoic acid ethyl ester 

Relevant academic research and scientific papers

Palladium-catalyzed cross-coupling reaction of organostannoates with aryl halides in aqueous medium

Water-soluble hydroxycomplexes 2, easily formed from organotin trihalides 1 in aqueous alkaline solution, react readily with aryl halides in the same medium in the presence of palladium complexes to give cross-coupled products 3 in high yields.

Cinnamic acid derivatives as inhibitors for chorismatases and isochorismatases

Chorismatases and isochorismatases catalyse the hydrolysis of chorismate or isochorismate leading to unsaturated cyclohexenoic acid derivatives. Based on simplification of the physiological substrates, two cinnamic acid-derived compounds, differing in the

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COMPOUNDS TO TREAT AMYLOIDOSIS AND PREVENT DEATH OF BETA-CELLS IN TYPE 2 DIABETES MELLITUS

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The water-soluble hydroxo complexes formed from organotrihalostannanes in aqueous alkali readily react in the presence of palladium in the same medium with aryl halides to give cross-coupling products in high yields.