115852-13-6Relevant articles and documents
Regioselective synthesis of multisubstituted furans via metalloradical cyclization of alkynes with α-diazocarbonyls: Construction of functionalized α-oligofurans
Cui, Xin,Xu, Xue,Wojtas, Lukasz,Kim, Martin M.,Zhang, X. Peter
supporting information, p. 19981 - 19984 (2013/02/23)
Co(III)-carbene radicals generated from activation of α- diazocarbonyls by Co(II)-porphyrin complexes have been shown to undergo a new type of tandem radical addition reaction with alkynes that affords five-membered furan structures. The Co(II) complex of
Catalyst-controlled ring-opening cycloisomerization reactions of cyclopropenyl carboxylates for highly regioselective synthesis of different 2-alkoxyfurans
Chen, Jie,Ma, Shengming
experimental part, p. 2415 - 2421 (2011/06/25)
Differently substituted 2-alkoxyfurans (2,3,4- or 2,3,5-trisubstituted furans) were highly regioselectively synthesized by means of the ring-opening cycloisomerization of the same cyclopropenyl carboxylates with good yields in different solvents and excel
RhII-catalyzed cycloadditions of carbomethoxy iodonium ylides
Batsila, Christina,Kostakis, George,Hadjiarapoglou, Lazaros P
, p. 5997 - 6000 (2007/10/03)
Carbomethoxy iodonium ylides, generated from methyl acetoacetate and methyl malonate, respectively, are exploited in synthesis of cyclopropanes, cyclopropenes as well as various heterocycles.
