Issue 24, 2009

Formation and [3,3]-sigmatropic rearrangement of O-allyl nitronic esters: a new route to γ,δ-unsaturated nitro compounds

Abstract

O-Allyl nitronic esters that are obtained from tin(IV) catalyzed Diels–Alder reactions undergo thermal rearrangement to γ,δ-unsaturated nitro compounds.

Graphical abstract: Formation and [3,3]-sigmatropic rearrangement of O-allyl nitronic esters: a new route to γ,δ-unsaturated nitro compounds

Supplementary files

Article information

Article type
Communication
Submitted
16 Feb 2009
Accepted
11 May 2009
First published
20 May 2009

Chem. Commun., 2009, 3531-3532

Formation and [3,3]-sigmatropic rearrangement of O-allyl nitronic esters: a new route to γ,δ-unsaturated nitro compounds

P. A. Wade, A. Pipic, M. Santhanaraman and H. T. Le, Chem. Commun., 2009, 3531 DOI: 10.1039/B902870F

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