80697-46-7Relevant academic research and scientific papers
Chalcogenopyranones from disodium chalcogenide additions to 1,4- pentadiyn-3-ones. The role of enol ethers as intermediates
Leonard, Kristi,Nelen, Marina,Raghu, Madhavi,Detty, Michael R.
, p. 707 - 717 (2007/10/03)
Enol ethers 9 are formed as a mixture of E- and Z-isomers from the addition of ethanol to 1,4-pentadiyn-3-ones 2 in sodium ethoxide/ethanol. The enol ethers react with disodium chalcogenides to give the corresponding 2,6- disubstituted chalcogenopyranones
Δ4,4'-4-CHALCOGENAPYRANYL-4H-CHALCOGENAPYRANS SYNTHESIS, ELECTROCHEMICAL OXIDATION, AND ESR INVESTIGATIONS OF RADICAL-CATION STATES
Detty, Michael R.,Hassett, James W.,Murray, Bruce J.,Reynolds, George A.
, p. 4853 - 4860 (2007/10/02)
The O-, S-, Se- and Te-containing Δ4,4'-2,2',6,6'-tetramethyl-, -tetra-t-butyl- and -tetraphenyl-4-(chalcogenapyranyl)-4H-chalcogenapyrans were prepared from the corresponding chalcogenapyran-4-ones.The thia-, selena- and tellurapyran-4-ones we
Telluropyrylium Dyes. 1. 2,6-Diphenyltelluropyrylium Dyes
Detty, Michael R.,Murray, Bruce J.
, p. 5235 - 5239 (2007/10/02)
Methine and polymethine dyes containing at least one 2,6-diphenyltelluropyrylo group as well as another 2,6-diphenylchalcogenopyrylo group have been prepared by the condensation of 2,6-diphenyl-4-methylchalcogenopyrylium salts with 4H-2,6-diphenyltellurop
