Influence of electrochemical conditions on the regio- and stereoselectivity of selenocyclization of alkenyl hydantoins Short Communication

Main Article Content

Biljana Šmit
http://orcid.org/0000-0001-9799-4723
Petar Stanić
https://orcid.org/0000-0002-3655-6452
Ljubinka Joksović
https://orcid.org/0000-0001-8781-6915
Darko Ašanin
https://orcid.org/0000-0003-1098-400X
Zoran Simić

Abstract

5-Alkenyl hydantoins and alkenyl spirohydantoins are converted into bicyclic and tricyclic hydantoins, under indirect electrochemical conditions, generating the phenylselenyl cation in situ. The reactions proceeded in good to exelent yields. The influence of electrochemical conditions on regio- and diastereoselectivity of the selenocyclization reactions is investigated.

Article Details

How to Cite
[1]
B. Šmit, P. Stanić, L. Joksović, D. Ašanin, and Z. Simić, “Influence of electrochemical conditions on the regio- and stereoselectivity of selenocyclization of alkenyl hydantoins: Short Communication”, J. Serb. Chem. Soc., vol. 86, no. 6, pp. 585-590, Jun. 2021.
Section
Electrochemistry

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