172841-59-7Relevant academic research and scientific papers
Gold-Catalyzed Cycloisomerization and Diels-Alder Reaction of 1,6-Diyne Esters with Alkenes and Diazenes to Hydronaphthalenes and -cinnolines
Yan, Jianming,Tay, Guan Liang,Neo, Cuien,Lee, Bo Ra,Chan, Philip Wai Hong
supporting information, p. 4176 - 4179 (2015/09/15)
A method for the efficient preparation of hydronaphthalene and -cinnoline derivatives by Au(I)-catalyzed cycloisomerzation of 1,6-diyne esters followed by a Diels-Alder reaction with alkenes or diazenes under mild conditions at room temperature with catal
Enantioselective preparation of 8-oxabicyclo[3.2.1]octane derivatives via asymmetric [3+2]-cycloaddition of platinum-containing carbonyl ylides with vinyl ethers
Ishida, Kento,Kusama, Hiroyuki,Iwasawa, Nobuharu
supporting information; experimental part, p. 8842 - 8843 (2010/08/21)
A catalytic asymmetric synthesis of 8-oxabicyclo[3.2.1]octane derivatives was achieved through the [3+2]-cycloaddition of the platinum-containing carbonyl ylides generated from acyclic γ,δ-ynones on treatment with 10 mol % of PtCl2-Walphos and
