Synthetic study of marine diterpenoid aberrarone: stereocontrolled construction of tetracyclic framework was written by Kobayashi, Toyoharu;Tokumoto, Kasumi;Tsuchitani, Yuki;Abe, Hideki;Ito, Hisanaka. And the article was included in Tetrahedron in 2015.Recommanded Product: 2-Bromomethyl-1,3-dioxolane This article mentions the following:
Highly stereocontrolled synthesis of the tetracyclic framework of the marine diterpenoid aberrarone (I), which possesses antimalarial activity against a chloroquine-resistant strain of Plasmodium, has been accomplished. A key feature of the synthesis is the complete stereocontrolled construction of C- and D-ring using stereoselective 1,4-addition followed by intramol. aldol reaction protocol. In the experiment, the researchers used many compounds, for example, 2-Bromomethyl-1,3-dioxolane (cas: 4360-63-8Recommanded Product: 2-Bromomethyl-1,3-dioxolane).
2-Bromomethyl-1,3-dioxolane (cas: 4360-63-8) belongs to dioxole derivatives. Dioxoles, particularly fluorinated dioxoles, are used as co-monomers to make polymers that find use in forming protective coatings for chemical resistance. Dioxole functionalized metal-organic frameworks have also been recently reported.Recommanded Product: 2-Bromomethyl-1,3-dioxolane
Referemce:
1,3-Benzodioxole – Wikipedia,
Dioxole | C3H4O2 – PubChem