Palladium-catalyzed desymmetric [2+2+2] cycloaddition of 1,6-enyne and alkyne was written by Zhao, Wei-Cheng;Wang, Xin;Feng, Juhua;Tian, Ping;He, Zhi-Tao. And the article was included in Tetrahedron in 2021.Electric Literature of C6H10O2 This article mentions the following:
A novel and straightforward palladium-catalyzed desym. [2+2+2] cycloaddition reaction of alkyne-tethered cyclohexadienone and internal alkyne is established. Widely existing fused tricyclic hydronaphthofuran and hydronaphthopyrrole frameworks are prepared diastereoselectively in moderate to excellent yields. One-step aromatization process provides a new and facile access to important benzene-containing tricycles from above cycloaddition products. In the experiment, the researchers used many compounds, for example, 1,4-Dimethoxy-2-butyne (cas: 16356-02-8Electric Literature of C6H10O2).
1,4-Dimethoxy-2-butyne (cas: 16356-02-8) belongs to ethers. Relative to alcohols, ethers are generally less dense, are less soluble in water, and have lower boiling points. They are relatively unreactive. Ethers are good solvents partly because they are not very reactive. Most ethers can be cleaved, however, by hydrobromic acid (HBr) to give alkyl bromides or by hydroiodic acid (HI) to give alkyl iodides.Electric Literature of C6H10O2
Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem