The University of Southampton
University of Southampton Institutional Repository

Enantioselective synthesis and selective monofunctionalization of (4R,6R)-4,6-dihydroxy-2,8-dioxabicyclo[3.3.0]octane

Enantioselective synthesis and selective monofunctionalization of (4R,6R)-4,6-dihydroxy-2,8-dioxabicyclo[3.3.0]octane
Enantioselective synthesis and selective monofunctionalization of (4R,6R)-4,6-dihydroxy-2,8-dioxabicyclo[3.3.0]octane
An efficient, enantioselective synthesis of a disubstituted bis-THF scaffold 5 is described, as well as an efficient differentiation of the 1,3-diol unit.
hiv protease inhibitors, stereocontrolled synthesis, aspergillus-stellatus, furofurans, metathesis, mycotoxin, arabitol
1523-7060
5821-5824
Linclau, Bruno
19b9cacd-b8e8-4c65-af36-6352cade84ba
Jeffery, Martin J.
4d9d91dc-9d4d-4063-8d72-35db99db3967
Josse, Solen
512a0636-acc9-41fa-a587-152bd8ca13b5
Tomassi, Cyrille
51fbf42e-4b91-481c-8528-95ca06e30c40
Linclau, Bruno
19b9cacd-b8e8-4c65-af36-6352cade84ba
Jeffery, Martin J.
4d9d91dc-9d4d-4063-8d72-35db99db3967
Josse, Solen
512a0636-acc9-41fa-a587-152bd8ca13b5
Tomassi, Cyrille
51fbf42e-4b91-481c-8528-95ca06e30c40

Linclau, Bruno, Jeffery, Martin J., Josse, Solen and Tomassi, Cyrille (2006) Enantioselective synthesis and selective monofunctionalization of (4R,6R)-4,6-dihydroxy-2,8-dioxabicyclo[3.3.0]octane. Organic Letters, 8 (25), 5821-5824. (doi:10.1021/ol062431d).

Record type: Article

Abstract

An efficient, enantioselective synthesis of a disubstituted bis-THF scaffold 5 is described, as well as an efficient differentiation of the 1,3-diol unit.

Full text not available from this repository.

More information

Published date: 2006
Keywords: hiv protease inhibitors, stereocontrolled synthesis, aspergillus-stellatus, furofurans, metathesis, mycotoxin, arabitol

Identifiers

Local EPrints ID: 44490
URI: http://eprints.soton.ac.uk/id/eprint/44490
ISSN: 1523-7060
PURE UUID: 2e1ff1ca-8610-4110-acec-8993356599e0
ORCID for Bruno Linclau: ORCID iD orcid.org/0000-0001-8762-0170

Catalogue record

Date deposited: 06 Mar 2007
Last modified: 20 Jul 2019 01:07

Export record

Altmetrics

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.

×