Issue 105, 2016, Issue in Progress

Tellurium-promoted stereoselective hydrodebromination of 1,1-dibromoalkenes: synthesis of (E)-bromoalkenes

Abstract

We describe herein an efficient and simple method for the stereoselective hydrodebromination of 1,1-dibromoalkenes by using a catalytic amount of the nucleophilic species of tellurium, generated in situ by the reaction of elemental tellurium with NaBH4. By this methodology, (E)-bromoalkenes were obtained in moderate to excellent yields under mild reaction conditions, without the use of transition metals or base. Furthermore, a high stereoselectivity for the (E)-isomer was observed when 1,1-dibromoarylalkenes were used, thus indicating a promising alternative for future applications in organic synthesis.

Graphical abstract: Tellurium-promoted stereoselective hydrodebromination of 1,1-dibromoalkenes: synthesis of (E)-bromoalkenes

Supplementary files

Article information

Article type
Paper
Submitted
29 Sep 2016
Accepted
25 Oct 2016
First published
26 Oct 2016

RSC Adv., 2016,6, 103657-103661

Tellurium-promoted stereoselective hydrodebromination of 1,1-dibromoalkenes: synthesis of (E)-bromoalkenes

G. Perin, Angelita M. Barcellos, T. J. Peglow, P. C. Nobre, R. Cargnelutti, E. J. Lenardão, F. Marini and C. Santi, RSC Adv., 2016, 6, 103657 DOI: 10.1039/C6RA24295B

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