76226-32-9Relevant articles and documents
Switchable synthesis of cyclic carbamates by carbon dioxide fixation at atmospheric pressure
Toda, Yasunori,Shishido, Minoru,Aoki, Tatsuya,Sukegawa, Kimiya,Suga, Hiroyuki
supporting information, p. 6672 - 6675 (2021/07/13)
The base-promoted switchable synthesis of five- and six-membered cyclic carbamates using atmospheric pressure carbon dioxide as the C1 source was developed. The chemoselectivity of products was simply controlled by changing bases and solvents. The reaction proceeds effectively under mild conditions, affording valuable cyclic carbamates. Experimental results and DFT studies revealed the reaction mechanism.
Substituted piperazines as novel potential radioprotective agents
Cizkova, Jana,Filipova, Alzbeta,Havelek, Radim,Jelicova, Marcela,Koutova, Darja,Kucera, Tomas,Majorosova, Martina,Marek, Jan,Muckova, Lubica,Pejchal, Jaroslav,Prchal, Lukas,Psotka, Miroslav,Rezacova, Martina,Sinkorova, Zuzana,Tichy, Ales,Zivna, Natalie
supporting information, (2020/02/11)
The increasing risk of radiation exposure underlines the need for novel radioprotective agents. Hence, a series of novel 1-(2-hydroxyethyl)piperazine derivatives were designed and synthesized. Some of the compounds protected human cells against radiation-
Enzyme- and ruthenium-catalyzed dynamic kinetic resolution involving cascade alkoxycarbonylations for asymmetric synthesis of 5-Substituted N-Aryloxazolidinones
Zhang, Yang,Xie, Sheng,Yan, Mingdi,Ramstr?m, Olof
, p. 138 - 144 (2019/04/10)
Asymmetric synthesis of N-aryloxazolidinones via dynamic kinetic resolution was developed. A ruthenium-based catalyst was used in the racemization of β-anilino alcohols, while Candida antarctica lipase B (CAL-B) was applied for two selective alkoxycarbony
