1314042-79-9

Upstream product

• 1314042-61-9 (4R,7S)-1-acryloyl-7-isopropyl-4-methyl-3-phenyl-4,5,6,7-tetrahydro-1H-indazole 
• 73210-14-7 N-chloro-N-sodio-tert-butylcarbamate 
• 2216-51-5 (-)-menthol 
• 10458-14-7 (2R,5S)-menthone 
• 155095-12-8 (3R,6S)-2-Benzoyl-3-methyl-6-isopropylcyclohexanone 
• 4248-19-5 tert-butyl carbazate 
• 155095-10-6 (4R,7S)-3-phenyl-4-methyl-7-isopropyl-4,5,6,7-tetrahydro-1H-indazole 

Downstream Products

• 126496-79-5 (S)-N-tert-butoxycarbonyl aziridine-2-carboxylate methyl ester 
• 155095-10-6 (4R,7S)-3-phenyl-4-methyl-7-isopropyl-4,5,6,7-tetrahydro-1H-indazole 

Relevant academic research and scientific papers

A practical method for the aziridination of α,β-unsaturated carbonyl compounds with a simple carbamate utilizing sodium hypochlorite pentahydrate

The efficient formation oftert-butylN-chloro-N-sodio-carbamate by the reaction of simpletert-butyl carbamate with sodium hypochlorite pentahydrate (NaOCl·5H2O) would be a practical and green method for the aziridination of α,β-unsaturated carbo

Diastereoselective aziridination of chiral electron-deficient olefins with N-chloro-N-sodiocarbamates catalyzed by chiral quaternary ammonium salts

Chiral quaternary ammonium salt-catalyzed diastereoselective aziridination of electron-deficient olefins that possess a chiral auxiliary with N-chloro-N-sodiocarbamates was developed. The key to high stereoselectivity was found to be the employment of the