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BY-NC-ND 3.0 license Open Access Published by De Gruyter June 2, 2014

Cyclization of Unsaturated Alcohols. Mild and Efficient Selenocyclization of Pent-4-en-1-ol

  • Marina D. Rvović , Vera M. Divac , Ninko Radenković and Zorica M. Bugarčić EMAIL logo

An innovative route for intramolecular cyclization of pent- 4-en-1-ol has been delineated through a ring closing reaction with phenylselenyl halides, in good yield. Several catalysts (triethylamine, quinoline, 2,2ʹ-bipyridine, pyridine, CoCl2 and SnCl2) enable fast, facile and efficient cyclization.

Graphical Abstract

 Cyclization of Unsaturated Alcohols. Mild and Efficient Selenocyclization of Pent-4-en-1-ol

Cyclization of Unsaturated Alcohols. Mild and Efficient Selenocyclization of Pent-4-en-1-ol

Received: 2011-11-4
Published Online: 2014-6-2
Published in Print: 2011-12-1

© 1946 – 2014: Verlag der Zeitschrift für Naturforschung

This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License.

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