Enantioselective synthesis of the dioxabicyclo[3.2.1]octane core of the zaragozic acids via intramolecular Wacker-type cyclisation reactions

Wacker-type cyclisation reactions provide an effective entry into the dioxabicyclo[3.2.1]octane core of the zaragozic acid analogues.

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Published in:Organic & biomolecular chemistry 2004-08, Vol.2 (15), p.2220-2228
Main Authors: Perlmutter, Patrick, Selajerern, Walailak, Vounatsos, Filisaty
Format: Article
Language:English
Subjects:
Antifungal Agents - chemical synthesis
Bridged Bicyclo Compounds, Heterocyclic - chemical synthesis
Cyclization
Farnesyl-Diphosphate Farnesyltransferase - antagonists & inhibitors
Molecular Structure
Octanes - chemical synthesis
Stereoisomerism
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container_issue 15
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container_title Organic & biomolecular chemistry
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creator Perlmutter, Patrick
Selajerern, Walailak
Vounatsos, Filisaty
description Wacker-type cyclisation reactions provide an effective entry into the dioxabicyclo[3.2.1]octane core of the zaragozic acid analogues.
doi_str_mv 10.1039/b406280a
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ispartof Organic & biomolecular chemistry, 2004-08, Vol.2 (15), p.2220-2228
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source Royal Society of Chemistry: Jisc Collections: Journals Archive 1841-2007 (2019-2023)
subjects Antifungal Agents - chemical synthesis
Bridged Bicyclo Compounds, Heterocyclic - chemical synthesis
Cyclization
Farnesyl-Diphosphate Farnesyltransferase - antagonists & inhibitors
Molecular Structure
Octanes - chemical synthesis
Stereoisomerism
title Enantioselective synthesis of the dioxabicyclo[3.2.1]octane core of the zaragozic acids via intramolecular Wacker-type cyclisation reactions
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