1127435-37-3

Upstream product

• 67093-66-7 (E)-3-hydroxy-5-phenyl-pent-4-enoic acid tert-butyl ester 
• 540-88-5 acetic acid tert-butyl ester 
• 14371-10-9 (E)-3-phenylpropenal 
• 100-52-7 benzaldehyde 
• 145090-91-1 tert-butyl 4-(diethoxyphosphoryl)-3-oxobutanoate 

Downstream Products

• 1454283-61-4 tert-butyl 3-styryl-2H-azirine-2-carboxylate 
• 1454283-83-0 5-tert-butyl 2-ethyl 4-phenyl-6-styrylpyridine-2,5-dicarboxylate 
• 4743-97-9 (E)-3-oxo-5-phenylpent-4-enoic acid 
• 1225057-31-7 (E)-tert-butyl 2-phenyl-5-styryloxazole-4-carboxylate 
• 1202447-89-9 (E)-tert-butyl 2-fluoro-3-oxo-5-phenylpent-4-enoate 

Relevant academic research and scientific papers

Synthesis of pyridines by carbenoid-mediated ring opening of 2H-azirines

Roaming the range: The title reaction tolerates a wide range of substituents on the resulting pyridine ring using mild reaction conditions (see scheme; esp=α,α,α′,α′-tetramethyl-1,3- benzenedipropionic acid). The formation of the key intermediate is catal

Deslongchamps annulations with benzoquinone monoketals

The so-called Deslongchamps annulation of deprotonated γ, δ-unsaturated β-ketoesters 15 to 2-(alkoxycarbonyl)cyclohex-2-en-1- ones or similarly activated cyclohex-2-en-1-ones offers a versatile access to various kinds of decalindiones. The scope of Deslon