866129-82-0

Upstream product

• 526197-85-3 4-tert-butyl-5-[3-(cyanomethyl)phenyl]-3,3-dimethyl-2,3-dihydrofuran 
• 866129-66-0 5-(3-bromophenyl)-4-tert-butyl-3,3-dimethyl-2,3-dihydrofuran 
• 866129-79-5 4-tert-butyl-5-[3-(1-cyanoethyl)phenyl]-3,3-dimethyl-2,3-dihydrofuran 
• 609-02-9 methyl-malonic acid dimethylester 
• 714964-21-3 5-tert-butyl-1-[3-(1-cyanoethenyl)phenyl]-4,4-dimethyl-2,6,7-trioxabicyclo[3.2.0]heptane 
• 866129-72-8 4-tert-butyl-5-[3-(hydroxymethyl)phenyl]-3,3-dimethyl-2,3-dihydrofuran 
• 866129-75-1 5-[3-(bromomethyl)phenyl]-4-tert-butyl-3,3-dimethyl-2,3-dihydrofuran 
• 866129-69-3 4-tert-butyl-5-(3-formylphenyl)-3,3-dimethyl-2,3-dihydrofuran 

Relevant academic research and scientific papers

Chemiluminescent decomposition of a dioxetane bearing a 3-(1-cyanoethenyl)phenyl moiety induced by Michael addition of an anion of malonate

A thermally stable dioxetane bearing a 3-(1-cyanoethenyl)phenyl group (1) was synthesized. Michael addition of an anion of malonate (3a,b) to a dioxetane (1) substituted with a 3-(1-cyanoethenyl)phenyl moiety took place to give an intermediary dioxetane b

Intramolecular charge-transfer-induced chemiluminescent decomposition of 1,2-dioxetanes bearing a phenylmethanide anion

Dioxetanes (1) bearing a phenyl moiety substituted with a methylène or methine having an electron-withdrawing group(s) (-CH2-Ew or -CH(X)-Ew) and dioxetane (2) bearing a 3-(l-cyanoethenyl)phenyl group were synthesized. Treatment of dioxetanes (