85388-85-8Relevant academic research and scientific papers
Gold(iii) promoted formation of dihydroquinazolinones: Double X-H activation by gold
Kadiyala, Veerabhushanam,Karunakar, Galla V.,Kumar, Perla Bharath,Raju, Chittala Emmaniel,Sridhar, Balasubramanian,Sunil, Komalla
, p. 35681 - 35691 (2020)
An efficient 2-furyl gold-carbene promoted synthetic method was developed for the formation of dihydroquinazolinones from enynones by dual insertion of anthranilamides. In this organic transformation a new C-O and two C-N bond formations occurred and dihy
Copper-catalyzed C-O bond formation: An efficient one-pot highly regioselective synthesis of furans from (2-furyl)carbene complexes
Cao, Hua,Zhan, Haiying,Cen, Jinghe,Lin, Jingxin,Lin, Yuanguang,Zhu, Qiuxia,Fu, Minling,Jiang, Huanfeng
supporting information, p. 1080 - 1083 (2013/03/29)
A convenient one-pot Cu(I)-catalyzed strategy for regioselective synthesis of trisubstituted furan derivatives has been developed via (2-furyl) carbene complexes. This process has opened a new synthetic route to a variety of α-carbonyl furans using air as
Synthesis of 2-acylfurans from 3-(1-alkynyl)-2-alken-1-ones via the oxidation of gold-carbene intermediates by H2O2
Wang, Tao,Zhang, Junliang
supporting information; experimental part, p. 4270 - 4273 (2010/07/04)
An efficient approach to 2,4,5-trisubstituted 2-acylfurans is described: treating 3-(1-alkynyl)-2-alken-1-ones with AuCl3 in DCM at rt in the presence of H2O2 afforded good yields of 2-acylfurans.
Reaction of selenonium ylides with activated acetylenes
Magdesieva, N. N.,Kyandzhetsian, R. A.,Gordeev, M. F.
, p. 2219 - 2227 (2007/10/02)
The reaction of dimethylaroylmethylselenonium bromides with dibenzoylacetylene in the presence of bases leads to the formation of a mixture of 2-aryl-3,5-diaroyl- and 2-aryl-4,5-diaroylfurans.The latter are easily converted into 2,4,7-triarylfuropy
