143364-69-6

Upstream product

• 72015-57-7 (Z)-2-(benzyloxycarbonylamino)but-2-enoic acid 

Downstream Products

• 143364-70-9 ((Z)-1-Thiocarbamoyl-propenyl)-carbamic acid benzyl ester 
• 1373888-88-0 methyl (Z)-2-[1-(((benzyloxy)carbonyl)amino)prop-1-en-1-yl]-5-isopropyloxazole-4-carboxylate 
• 1373888-89-1 methyl (Z)-2-[1-(((benzyloxy)carbonyl)amino)prop-1-en-1-yl]-5-phenyloxazole-4-carboxylate 
• 1373888-87-9 methyl (Z)-2-[1-(((benzyloxy)carbonyl)amino)prop-1-en-1-yl]-5-methyloxazole-4-carboxylate 
• 1373888-71-1 ethyl (Z)-2-[1-((1-(benzyloxy)carbonyl)amino)prop-1-en-1-yl]oxazole-4-carboxylate 
• 143364-71-0 (Cbz)-(ΔAbu)Thz-OEt 

Relevant academic research and scientific papers

Convenient Syntheses of Thiazoles Incorporated with α-Dehydroamino Acid and Dehydropeptide Structures

The convenient syntheses of various thiazole α-dehydroamino acids, thiazole valine ethyl ester, and their dehydrodi- and tripeptides, which are important moieties and segment of micrococcin P1 and noshiheptide, macrocyclic peptide antibiotics,

Scope and limitations of a modified hantzsch reaction for the synthesis of oxazole-dehydroamino acid derivatives from dehydroamino acid amides

A variety of oxazole derivatives that possess an α,β-unsaturated substituent at the 2-position were conveniently synthesized in good yields via a Hantzsch-type reaction between dehydroamino acid amides and β-bromopyruvate derivatives. Furthermore, oxazole