866129-67-1

Downstream Products

• 866129-70-6 4-tert-butyl-5-(4-formylphenyl)-3,3-dimethyl-2,3-dihydrofuran 
• 866129-73-9 4-tert-butyl-5-[4-(hydroxymethyl)phenyl]-3,3-dimethyl-2,3-dihydrofuran 
• 866129-76-2 4-tert-butyl-5-[4-(bromomethyl)phenyl]-3,3-dimethyl-2,3-dihydrofuran 
• 866129-78-4 4-tert-butyl-5-[4-(cyanomethyl)phenyl]-3,3-dimethyl-2,3-dihydrofuran 
• 526198-09-4 5-tert-butyl-1-[4-(cyanomethyl)phenyl]-4,4-dimethyl-2,6,7-trioxabicyclo[3.2.0]heptane 

Relevant academic research and scientific papers

Base-induced cyclization of 1-benzyloxy-2,2,4,4-tetramethylpentan-3-ones: Intramolecular nucleophilic addition of an anion of a benzyl ether to the carbonyl moiety without the Wittig rearrangement or protophilic decomposition

Alkyl benzyl ethers bearing a carbonyl moiety in the alkyl chain (1) cyclize effectively, without the Wittig rearrangement or protophilic decomposition, to give hydroxytetrahydrofurans (trans-2) on treatment with ButOK in DMSO at room temperatu

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 (