68342-69-8

Upstream product

• 93638-44-9 phenyl(2-phenylaziridin-1-yl)methanone 
• 10026-13-8 phosphorus pentachloride 
• 34119-82-9 2-(benzoylamino)-1-phenylethanol 
• 4190-14-1 N-(2-oxo-2-phenylethyl)benzamide 
• 4633-92-5 β-chloro-phenethylamine 
• 98-88-4 benzoyl chloride 
• 100-42-5 styrene 
• 55-21-0 benzamide 

Downstream Products

• 3278-14-6 N-phenethylbenzamide 
• 128600-81-7 9-(2-Benzamido-1-phenylethyl)-9,10-dihydroanthracene 

Relevant academic research and scientific papers

Direct synthesis of oxazolines from olefins and amides using t-BuOI

A new and simple method for the synthesis of oxazolines from readily accessible olefins and amides using tert-butyl hypoiodite is described; aromatic/aliphatic olefins and amides can be used in the reaction to give a variety of oxazolines. The Royal Socie

Intermediate Substitution in the Formation of a Benzylic Anion by an Aromatic Radical Anion as Observed with 1-Benzoyl-2-phenylaziridine

The reaction of the title compound 1 with anthracene hydride AH(-) or anthracenide A(-*) leads to the formation of the benzylic anion 9 by fragmentation of the first generated substitution intermediate 7 or 8.In the reactions with AH(-) the carbanion 9 is completely trapped by protonation with dihydroanthracene AH2 yielding the reduction product 3 (N-benzoyl-phenethylamine).In reactions with A(-*) as well as with naphthalenide N(-*) the carbanion 9 either abstracts a proton from the solvent THF (yielding 3) or adds to the benzoyl group of unreacted 1 which finally results in β-benzamido-α-phenylpropiophenone (6).