853406-73-2

Upstream product

• 233750-51-1 methyl 2-(3-{tert-butyldiphenylsilyloxy}propyl)-1,3-oxazole-4-carboxylate 
• 233750-78-2 2-[3-(tert-butyl-diphenyl-silanyloxy)-propyl]-oxazole-4-carboxylic acid 
• 853406-71-0 2-[3-(tert-butyl-diphenyl-silanyloxy)-propyl]-4,5-dihydro-oxazole-4-carboxylic acid methyl ester 
• 853406-72-1 2-({2-[3-(tert-butyl-diphenyl-silanyloxy)-propyl]-oxazole-4-carbonyl}-amino)-3-hydroxy-propionic acid ethyl ester 

Downstream Products

• 853406-74-3 2'-[3-(tert-butyl-diphenyl-silanyloxy)-propyl]-[2,4']bioxazolyl-4-carboxylic acid ethyl ester 
• 233750-48-6 2'-[3-(tert-butyl-diphenyl-silanyloxy)-propyl]-[2,4']bioxazolyl-4-carbaldehyde 

Relevant academic research and scientific papers

Dehydrative cyclization of serine, threonine, and cysteine residues catalyzed by molybdenum(VI) oxo compounds

Commercially available molybdenum(VI) oxides such as (NH4)2MoO4, (NH4)6Mo7O24·4H2O, MoO2(acac)2, and MoO2(TMHD)2 are highly

Molybdenum oxides as highly effective dehydrative cyclization catalysts for the synthesis of oxazolines and thiazolines

(Chemical Equation Presented) In the presence of molybdenum oxide the dehydrative cyclization of N-acylserines, N-acylthreonines, and N-acylcysteines can be carried out under Dean-Stark conditions in toluene to give oxazolines and thiazolines. The ammoniu