Issue 6, 2013

Nucleophilic substitution of bromonorbornenes and derivatives by electron transfer reactions

Abstract

The photoinitiated substitution reactions of anti-7-bromobenzonorbornadiene (5), its syn isomer 6, exoanti-13-bromobenzocyclobutanorbornene (7), syn-7-bromonorbornene (8) and bromonorbornane (9) with Me3Sn and Ph2P anions, in liquid ammonia, are here informed to occur with good yields of substitution. The stereochemical outcome is discussed in terms of calculations with the B3LYP functional and the 6-31+G* basis set; the solvent being included as a continuum through the PCM model. The experimental relative chemical reactivity of pairs of substrates toward a given anion is also presented.

Graphical abstract: Nucleophilic substitution of bromonorbornenes and derivatives by electron transfer reactions

Supplementary files

Article information

Article type
Paper
Submitted
07 Sep 2012
Accepted
03 Dec 2012
First published
04 Dec 2012

Org. Biomol. Chem., 2013,11, 955-965

Nucleophilic substitution of bromonorbornenes and derivatives by electron transfer reactions

K. F. Crespo Andrada, L. E. Peisino, M. Güney, A. Daştan and A. B. Pierini, Org. Biomol. Chem., 2013, 11, 955 DOI: 10.1039/C2OB26768C

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements