WebApr 19, 2012 · A method of preparing a cyclic monomer, comprising: forming a first mixture comprising a precursor compound, bis (pentafluorophenyl)carbonate, and a catalyst; wherein the precursor compound has a structure comprising a) two or more carbons, and b) two functional groups selected from the group consisting of primary amine, secondary … WebJan 31, 2024 · As for cyclic thiocarbonate 10, photoredox catalysts were ineffective to promote radical deoxygenation of thioimidazole 14; however, by using the Oshimás …
The catalyst systems for COS/epoxide copolymerization. a Metal...
WebThe polymerization was carried out with 2 mol% of trifluoromethanesulfonic acid, methyl trifluoromethanesulfonate, boron trifluoride etherate, or triethyloxonium tetrafluoroborate … WebJan 17, 2003 · The cationic ring‐opening polymerization of TC2 did not proceed with trifluoromethanesulfonic acid, methyl trifluoromethanesulfonate, triethyloxonium … baju nikah 2022
Chemoselective ring-opening copolymerization of five …
WebAug 1, 2024 · Design concepts of our catalytic systems were discussed based on experimental results. Our catalytic system could also be applied to cyclic thiocarbonate synthesis by the use of carbon disulfide... WebDec 11, 2013 · The key steps of this synthetic method involve the formation of a cyclic thiocarbonate and the regioselective radical opening of the thiocarbonate to yield the corresponding primary alcohol –CF 2 CH 2OH. Using this synthetic method, novel fluorinated analogs of ganciclovir and penciclovir have been prepared. Graphical abstract Web1. The 1,2-diol is converted to the cyclic thiocarbonate derivative using thiocarbonyldiimidazole, TCDI. 2. Cis-elimination reaction upon treatment with excess trimethylphosphite. 2.1. The phosphite attacks the sulfur atom leaving a carbene. 2.2. The carbene reacts with a second equivalent of phosphite, generating an ylide. 2.3. baju nikah 2023