206064-59-7

Upstream product

• 194286-83-4 3-ethoxy-4-methylisoxazole-5-carboxamide 
• 166180-70-7 (3-ethoxy-4-methylisoxazol-5-yl)carboxylic acid 
• 166180-69-4 3-ethoxy-5-hydroxymethyl-4-methylisoxazol 
• 194286-80-1 5-Bromomethyl-3-ethoxy-4-methyl-isoxazole 
• 127020-26-2 3-ethoxy-4,5-dimethylisoxazol 
• 76-83-5 trityl chloride 
• 194286-89-0 3-(3-Ethoxy-4-methylisoxazol-5-yl)-1H-1,2,4-triazole 

Downstream Products

• 194287-00-8 ethyl 2-acetamido-3-[3-ethoxy-5-(1-trityl-1H-1,2,4-triazol-3-yl)isoxazol-4-yl]-2-(ethoxycarbonyl)propionate 
• 194286-99-2 3-[4-(Bromomethyl)-3-ethoxyisoxazol-5-yl]-1-trityl-1H-1,2,4-triazole 

Relevant academic research and scientific papers

3-Alkoxyisoxazol-4-yl-substituted 2-amino carboxylic acid compounds

(3-Alkoxyisoxazol-4-yl)-substituted 2-amino carboxylic acid derivatives and sulfur analogues thereof having general formula (I) or (II), wherein R1is hydrogen, alkyl, alkenyl, alkynyl, cycloalk(en)yl, cycloalk(en)yl-alk(en/yn)yl or optionally s

Heteroaryl analogues of AMPA. Synthesis and quantitative structure- activity relationships

A number of 3-isoxazolol bioisosteres, 7a-i, of (S)-glutamic acid (Glu), in which the methyl group of (RS)-2-amino-3-(3-hydroxy-5-methylisoxazol-4- yl)propionic acid (AMPA, 1) was replaced by different 5-membered heterocyclic rings, were synthesized. Comp