3,4-Unsubstituted 2-<i>tert</i>-Butyl-pyrrolidine-1-oxyls with Hydrophilic Functional Groups in the Side Chains

Pyrrolidine nitroxides with four bulky alkyl substituents adjacent to N–O group are known for their high resistance to bioreduction. The 3,4-unsubstituted 2-<i>tert</i>-butyl-2-ethylpyrrolidine-1-oxyls were prepared from the corresponding 2-<i>tert</i>-butyl-1-pyrroline-1-oxides via either the addit...

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Auteurs principaux:	Andrey I. Taratayko, Yurii I. Glazachev, Ilia V. Eltsov, Elena I. Chernyak, Igor A. Kirilyuk
Format:	Artigo
Langue:	Inglês
Publié:	MDPI AG 2022-03-01
Collection:	Molecules
Sujets:	nitroxides nitrones organometallic compounds pyrrolidine reduction kinetics
Accès en ligne:	https://www.mdpi.com/1420-3049/27/6/1922
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