25294-56-8Relevant articles and documents
Facile synthesis of 3(2H)-furanones
Panda, Niranjan,Nayak, Dinesh K.
, p. 1093 - 1100 (2018/02/22)
Abstract: A practical method for the synthesis of 3(2H)-furanones including the bullatenone was described. Intramolecular cyclization of 4-hydroxyalkynones in the presence of KOH affords the biologically potent furanones in moderate-to-good yield at room temperature. Synthesis of 4-hydroxyalkynones from the reaction of acid chloride and terminal alkyne in the presence of copper iodide at room temperature was also reported.
Cationic gold(I)-catalyzed intramolecular cyclization of γ-hydroxyalkynones into 3(2H)-furanones
Egi, Masahiro,Azechi, Kenji,Saneto, Moriaki,Shimizu, Kaori,Akai, Shuji
supporting information; experimental part, p. 2123 - 2126 (2010/06/12)
"Chemical Equation Presented" The combination of (p-CF 3C6H4)3PAuCl and AgOTf generates a powerful catalyst for the intramolecular cyclizations of readily available y-hydroxyalkynones un-der mild conditions. The
A NEW AND FACILE SYNTHESIS OF 3(2H)-FURANONES VIA CARBOXYLATION-DECARBOXYLATION SEQUENCE
Inoue, Yoshio,Ohuchi, Kunihiro,Imaizumi, Shin
, p. 5941 - 5942 (2007/10/02)
One-pot synthesis of 3(2H)-furanones from α-ethynyl tertiary alcohols and acyl halides has been achieved in the presence of a palladium complex under CO2 pressure.