22495-85-8Relevant academic research and scientific papers
Efficient Diels-Alder reaction of 1,2-benzoquinones with arynes and its utility in one-pot reactions
Kaicharla, Trinadh,Bhojgude, Sachin Suresh,Biju, Akkattu T.
supporting information, p. 6238 - 6241 (2013/02/25)
A new protocol for the efficient Diels-Alder reaction of 1,2-benzoquinones with arynes is reported. The aryne generated by the fluoride-induced 1,2-elimination of 2-(trimethylsilyl)aryl triflates undergoes a facile Diels-Alder reaction with 1,2-benzoquinones, affording the dioxobenzobicyclooctadienes in moderate to excellent yields. In addition, this methodology has been applied to the one-pot synthesis of benzoquinoxalinobarrelene and naphthalene derivatives.
The alkylation of naphthalene over one-dimensional fourteen-membered ring zeolites. the influence of zeolite structure and alkylating agent on the selectivity for dialkylnaphthalenes
Sugi, Yoshihiro,Maekawa, Hiroyoshi,Naiki, Hiroaki,Komura, Kenichi,Kubota, Yoshihiro
experimental part, p. 1166 - 1174 (2009/05/06)
The alkylation, i.e., isopropylation, s-butylation, and t-butylation, of naphthalene (NP) was examined over one-dimensional fourteen-membered (14-MR) zeolites: CIT-5 (CF1), UTD-1 (DON), and SSZ-53 (SFH), and compared to the results over H-mordenite (MOR)
