942232-49-7

Upstream product

• 645-00-1 m-iodonitrobenzene 
• 1663-39-4 tert-Butyl acrylate 
• 5765-65-1 4-(benzoyloxy)morpholine 
• 99-61-6 3-nitro-benzaldehyde 
• 59159-39-6 (tert-butoxycarbonylmethyl)triphenylphosphonium bromide 

Downstream Products

• 269071-88-7 (3-amino-phenyl)-propionic acid tert-butyl ester 
• 555-68-0 m-Nitrocinnamic Acid 
• 942232-07-7 C₃₅H₄₆N₄O₅ 
• 528884-89-1 3-(3-(2-(5-cyclohexyl-1-(2-cyclopentyl-2-oxo-ethyl)-2-oxo-1,2-dihydro-3H-1,3,4-benzotriazepin-3-yl)-acetylamino)-phenyl)-propionic acid 
• 528883-32-1 3-(3-(2-(5-cyclohexyl-1-(3,3-dimethyl-2-oxo-butyl)-2-oxo-1,2-dihydro-3H-1,3,4-benzotriazepin-3-yl)-acetylamino)-phenyl)-propionic acid 
• 942232-18-0 C₃₆H₄₆N₄O₅ 

Relevant academic research and scientific papers

Complementary site-selectivity in arene functionalization enabled by overcoming the ortho constraint in palladium/norbornene catalysis

Achieving site-selectivity in arene functionalization that is complementary to the site-selectivity from electrophilic aromatic substitution reactions has been a long-standing quest in organic synthesis. Palladium/norbornene cooperative catalysis potentia

Fabrication of Pd/CuFe2O4 hybrid nanowires: A heterogeneous catalyst for Heck couplings

The development of environmentally benign transformations is indispensable in organic synthesis. Herein, a hybrid heterogeneous catalyst, palladium(0) on copper ferrite nanowires, has been synthesized, characterized, and for the first time, employed in the Jeffrey Heck reaction between iodoarenes and allylic alcohols, and good to excellent yields have been obtained. In addition, the catalyst was found to be suitable for the usual Heck coupling. The nanocatalyst was recovered and reused up-to multiple runs without any noticeable loss of its catalytic activity.

CINNAMOYL INHIBITORS OF TRANSGLUTAMINASE

A compound of Formula, (I) or Formula: (II)