The University of Southampton
University of Southampton Institutional Repository

Samarium diiodide mediated intramolecular cyclisation of mixed enone-enoate systems: a simple preparation of spirocyclic ethers

Samarium diiodide mediated intramolecular cyclisation of mixed enone-enoate systems: a simple preparation of spirocyclic ethers
Samarium diiodide mediated intramolecular cyclisation of mixed enone-enoate systems: a simple preparation of spirocyclic ethers
Samarium(II) diiodide mediated intramolecular cyclisation of mixed enone–enoate substrates in THF/MeOH is described. Spirocyclic ethers are obtained, and the stereodefined preparation of 1-oxaspiro[4.4]nonan-7-one products is included.

samarium(II) diiodide, reductive cyclisation, michael addition, spirocycle, chelation control
0040-4039
928-931
Meng, Junxiu
4826e3e4-b519-4040-b4ab-98f24358f08a
Light, Mark E.
cf57314e-6856-491b-a8d2-2dffc452e161
Kilburn, Jeremy D.
e64ded70-825a-40ec-816b-c4605e007e7a
Dixon, Sally
943160fc-1b70-4c29-b2e3-b7785cee8a0c
Meng, Junxiu
4826e3e4-b519-4040-b4ab-98f24358f08a
Light, Mark E.
cf57314e-6856-491b-a8d2-2dffc452e161
Kilburn, Jeremy D.
e64ded70-825a-40ec-816b-c4605e007e7a
Dixon, Sally
943160fc-1b70-4c29-b2e3-b7785cee8a0c

Meng, Junxiu, Light, Mark E., Kilburn, Jeremy D. and Dixon, Sally (2011) Samarium diiodide mediated intramolecular cyclisation of mixed enone-enoate systems: a simple preparation of spirocyclic ethers. Tetrahedron Letters, 52 (8), 928-931. (doi:10.1016/j.tetlet.2010.12.077).

Record type: Article

Abstract

Samarium(II) diiodide mediated intramolecular cyclisation of mixed enone–enoate substrates in THF/MeOH is described. Spirocyclic ethers are obtained, and the stereodefined preparation of 1-oxaspiro[4.4]nonan-7-one products is included.

This record has no associated files available for download.

More information

Published date: 23 February 2011
Keywords: samarium(II) diiodide, reductive cyclisation, michael addition, spirocycle, chelation control

Identifiers

Local EPrints ID: 176335
URI: http://eprints.soton.ac.uk/id/eprint/176335
ISSN: 0040-4039
PURE UUID: 778ca998-512d-46c2-82db-9d594cf40425
ORCID for Mark E. Light: ORCID iD orcid.org/0000-0002-0585-0843
ORCID for Sally Dixon: ORCID iD orcid.org/0000-0003-2219-3635

Catalogue record

Date deposited: 08 Mar 2011 10:16
Last modified: 14 Mar 2024 02:46

Export record

Altmetrics

Contributors

Author: Junxiu Meng
Author: Mark E. Light ORCID iD
Author: Jeremy D. Kilburn
Author: Sally Dixon ORCID iD

Download statistics

Downloads from ePrints over the past year. Other digital versions may also be available to download e.g. from the publisher's website.

View more statistics

Atom RSS 1.0 RSS 2.0

Contact ePrints Soton: eprints@soton.ac.uk

ePrints Soton supports OAI 2.0 with a base URL of http://eprints.soton.ac.uk/cgi/oai2

This repository has been built using EPrints software, developed at the University of Southampton, but available to everyone to use.

We use cookies to ensure that we give you the best experience on our website. If you continue without changing your settings, we will assume that you are happy to receive cookies on the University of Southampton website.

×