1174657-32-9

Upstream product

• 100-52-7 benzaldehyde 
• 120157-94-0 N-(tert-butoxycarbonyl)p-methoxybenzylamine 
• 86269-11-6 (Tributylstannyl)methyl methanesulfonate 
• 70-11-1 α-bromoacetophenone 
• 98-86-2 acetophenone 
• 2393-23-9 4-methoxy-benzylamine 
• 112698-36-9 2-<(4-methoxybenzyl)amino>-1-phenylethanone 
• 24424-99-5 di-tert-butyl dicarbonate 
• 81316-56-5 N-<(β-hydroxy-2-phenyl)ethyl>-(4-methoxyphenyl)methylamine 
• 96-09-3 styrene oxide 

Downstream Products

• 1174657-45-4 C₃₁H₃₄F₃NO₆ 
• 1345986-01-7 2-(tert-butoxycarbonyl(4-methoxybenzyl)amino)-1-phenylethyl 4-fluorobenzenesulfonate 
• 1345986-00-6 2-(tert-butoxycarbonyl(4-methoxybenzyl)amino)-1-phenylethyl 3-nitrobenzenesulfonate 

Relevant academic research and scientific papers

Synthesis and 2D QSAR of O-sulphonated β-aminols derivatives as novel antifungal and antibacterial agents

Synthesis of a series of b-aminol derivatives using regioselective opening reaction catalyzed by SiO2 (60-120 mesh) and O-sulphonation in THF-KOH system, comprising tert-butoxycarbonyl at secondary nitrogen and evaluate for various stains of bacteria and fungi. SAR study of synthesized compound using backward regression analysis.

Preparation of enantiopure chiral amino- [D1]methyllithium compounds and determination of their micro- and macroscopic configurational stabilities

Chiral amino-[D1]methyllithiums have been tested with regard to their microscopic and macroscopic configurational stabilities. The N-Boc-N-diethoxyphosphinyl-sub-stituted analogue immediately rearranged, showing complete retention of configuration at up t