1192017-87-0

Upstream product

• 7563-05-5 4,4-dimethyl-2-phenyl-5-oxazolone 
• 6638-79-5 N,O-dimethylhydroxylamine*hydrochloride 
• 98-88-4 benzoyl chloride 
• 57224-51-8 N-benzoyl-2-methylalanine 

Downstream Products

• 1192017-88-1 N-[3-(2,4-dichloro-phenyl)-1,1-dimethyl-2-oxo-propyl]-benzamide 
• 1260435-39-9 N-(2-methyl-3-oxo-5-phenylpent-4-yn-2-yl)benzamide 
• 1260435-46-8 C₁₁H₁₂FNO 
• 1260435-47-9 5-ethyl-5-fluoro-4,4-dimethyl-2-phenyl-4,5-dihydrooxazole 
• 1260435-48-0 5-fluoro-4,4-dimethyl-2-phenyl-5-(prop-1-en-2-yl)-4,5-dihydrooxazole 
• 1260435-49-1 5-fluoro-4,4-dimethyl-2-phenyl-5-(phenylethynyl)-4,5-dihydrooxazole 
• 1260435-55-9 5,5-dimethyl-3-phenyl-6-(prop-1-en-2-yl)-4,5-dihydro-1,2,4-triazine 
• 1260435-57-1 5,5-dimethyl-3-phenyl-5,6-dihydro-4H-1,2,4-oxadiazin-6-ol 
• 1260435-58-2 5,5-dimethyl-3-phenyl-6-(phenylethynyl)-5,6-dihydro-4H-1,2,4-oxadiazin-6-ol 
• 35017-00-6 N-(2-methyl-1-oxopropan-2-yl)benzamide 
• 1260435-38-8 N-(2,4-dimethyl-3-oxopent-4-en-2-yl)benzamide 

Relevant academic research and scientific papers

DAST-mediated cyclization of α,α-disubstituted-α- acylaminoketones: Efficient and divergent synthesis of unprecedented heterocycles

The design of a new potent nonsteroidal ecdysone agonist led to the discovery of a diethylaminosulfur trifluoride (DAST)-mediated cyclization of α,α-disubstituted-α-acylaminoketones. The resulting fluorooxazolines can be ring-opened or selectively substit

NOVEL MICROBIOCIDES

Compounds of formula (I), in which the substituents are as defined in claim 1, are suitable for use as microbiocides.