Reference of 1,3,5,7-Tetramethyl-6-phenyl-2,4,8-trioxa-6-phosphaadamantane. The mechanism of aromatic electrophilic substitution of aromatic heterocycles is consistent with that of benzene. Compound: 1,3,5,7-Tetramethyl-6-phenyl-2,4,8-trioxa-6-phosphaadamantane, is researched, Molecular C16H21O3P, CAS is 97739-46-3, about Palladium-catalyzed C-O and C-C coupling reactions of electron-rich indoles. Author is Schwarz, Nicolle; Pews-Davtyan, Anahit; Alex, Karolin; Tillack, Annegret; Beller, Matthias.
A novel palladium-catalyzed formation of indole aryl ethers is described. In general, the corresponding indole ethers are obtained in the presence of Pd(OAc)2 combined with N-phenyl-2-(di-1-adamantylphosphino)pyrrole in high yields.
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Reference:
Tetrahydropyran – Wikipedia,
Tetrahydropyran – an overview | ScienceDirect Topics