863666-15-3

Upstream product

• 2687-43-6 O-benzylhydoxylamine hydrochloride 
• 150-13-0 4-amino-benzoic acid 
• 66493-39-8 4-(N-tert-butoxycarbonyl)aminobenzoic acid 
• 863666-11-9 tert-butyl (4-((benzyloxy)carbamoyl)phenyl)carbamate 

Downstream Products

• 863666-20-0 N-benzyloxy-4-phenylacetylamino-benzamide 
• 934832-29-8 N-benzyloxy-4-(2-methyl-2-phenyl-propionylamino)-benzamide 
• 934832-52-7 N-benzyloxy-4-(2,2-dimethyl-4-phenyl-butyrylamino)-benzamide 
• 934838-62-7 N-benzyloxy-4-(3-methyl-2-phenyl-butyrylamino)-benzamide 
• 863666-22-2 N-benzyloxy-4-(5-phenyl-pentanoylamino)-benzamide 
• 934838-32-1 N-benzyloxy-4-(2-phenyl-butyrylamino)-benzamide 
• 863666-21-1 N-benzyloxy-4-(3-phenyl-propionylamino)-benzamide 
• 935881-37-1 N-hydroxy-4-((R)-3-methyl-2-phenyl-butyrylamino)benzamide 
• 935881-37-1 AR-42 
• 863666-19-7 4-Benzoylamino-N-benzyloxy-benzamide 
• 934838-72-9 N-benzyloxy-4-(3-methyl-2-phenyl-butyrylamino)-benzamide 
• 934832-95-8 N-benzyloxy-4-(2-phenyl-butyrylamino)-benzamide 

Relevant academic research and scientific papers

From C1 to C3: Copper-Catalyzed gem-Bis(trifluoromethyl)olefination of α-Diazo Esters with TMSCF3

A Cu-catalyzed gem-bis(trifluoromethyl)olefination of α-diazo esters, using TMSCF3 as the only fluorocarbon source, has been developed and provides an exquisite method to access gem-bis(trifluoromethyl)alkenes. This unprecedented olefination pr

Structure-based optimization of phenylbutyrate-derived histone deacetylase inhibitors

Previously, we developed a strategy to develop a novel class of histone deacetylase (HDAC) inhibitors by tethering short-chain fatty acids with Zn 2+-chelating motifs, which led to N-hydroxy-4-(4-phenylbutyryl-amino) benzamide (HTPB), a hydroxa