1416916-85-2

Upstream product

• 1416916-82-9 (S)-1-((1-((3,5-di-tert-butyl-4-methoxyphenyl)sulfonyl)-4,4-dimethylpyrrolidin-2-yl)methoxy)-2,2,6,6-tetramethylpiperidine 
• 1416916-78-3 3,5-di-tert-butyl-N-(2,2-dimethylpent-4-en-1-yl)-4-methoxybenzenesulfonamide 
• 73604-46-3 2,2-dimethyl-1-amino-pent-4-ene 
• 160252-94-8 3,5-di-tert-butyl-4-methoxybenzene-1-sulfonyl chloride 

Relevant academic research and scientific papers

Mechanistic analysis and optimization of the copper-catalyzed enantioselective intramolecular alkene aminooxygenation

The catalytic asymmetric aminooxygenation of alkenes provides an efficient and straightforward approach to prepare chiral vicinal amino alcohols. We have reported a copper(II)-catalyzed enantioselective intramolecular alkene aminooxygenation, using (2,2,6