408341-83-3

Upstream product

• 206055-84-7 [(5RS)-3-(4-methoxyphenyl)-4,5-dihydroisoxazol-5-yl]methanol 
• 38435-51-7 N-hydroxy-4-methoxy-benzenecarboximidoyl chloride 
• 154614-91-2 (5R)-5-hydroxymethyl-3-(p-methoxyphenyl)-4,5-dihydroisoxazole 
• 408341-82-2 [(5R)-3-(4-methoxyphenyl)-4,5-dihydroisoxazol-5-yl]methyl mesylate 

Relevant academic research and scientific papers

Mechanistic Insights into the Racemization of Fused Cyclopropyl Isoxazolines

Experimental and computational studies of the unexpected racemization of enantiopure fused cyclopropyl isoxazolines are reported. These studies offer insights into the mechanism of racemization, quantify the position of the transition state on the dipolar

Stereocontrolled approaches to 2-(2-aminoalkyl)-1-hydroxycyclopropanes

(1S,2S)-2[(S)-Amino(4-methoxyphenyl)methyl]cyclopropan-1-ol together with a range of racemic 2-(2-aminoalkyl)-1-hydroxycyclopropanes were prepared by a stepwise procedure involving a 1,3-dipolar cycloaddition of a nitrile oxide to a cyclopropene followed