Application of 95715-86-9, Catalysts function by providing an alternate reaction mechanism that has a lower activation energy than would be found in the absence of the catalyst. In some cases, the catalyzed mechanism may include additional steps.In a article, 95715-86-9, molcular formula is C12H21NO5, introducing its new discovery.
A 5-step synthesis of alpha-alkoxymethyl-, alpha-siloxymethyl-and alpha- (carbamoyloxy)methyl-substituted enediynes 7 from type 23 beta-oxo esters was developed following the strategy of Scheme 2. Specifically, the beta-oxo esters 33, 36 and 38 (prepared as shown in Scheme 4) and NaH (or t-BuLi) gave Z- enolates in THF and E-enolates in DMF which were scavenged as enol triflates Z-27a-c and E-27a-c, respectively, upon treatment with triflimides 40 or 41 (Scheme 5). The Z-configurated enol triflates underwent Cacchi couplings with (trimethylsilyl)acetylene to give the pent-2-en-4-yne-1-carboxylates E-42a-c (Scheme 5). These were reduced to the corresponding aldehydes E-44a-c (Scheme 6) which were homologated with lithio(trimethylsilyl)diazomethane to furnish the desired enediynes 45a-c as pure E-isomers.
The proportionality constant is the rate constant for the particular unimolecular reaction. the reaction rate is directly proportional to the concentration of the reactant. I hope my blog about 95715-86-9 is helpful to your research. Related Products of 95715-86-9
Reference：
Oxazolidine – Wikipedia,
Oxazolidine | C3H2515NO – PubChem