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

Patrick Perlmutter; Walailak Selajerern; Filisaty Vounatsos

doi:10.1039/b406280a

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

Patrick Perlmutter, Walailak Selajerern, Filisaty Vounatsos

School of Chemistry

Research output: Contribution to journal › Article › Research › peer-review

26 Citations (Scopus)

Abstract

Wacker-type cyclization reactions provide an effective entry into the dioxabicyclo[3.2.1]octane core of the zaragozic acid analogs. [on SciFinder(R)]

Original language	English
Pages (from-to)	2220 - 2228
Number of pages	9
Journal	Organic & Biomolecular Chemistry
Volume	2
Issue number	15
DOIs	https://doi.org/10.1039/b406280a
Publication status	Published - 2004

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10.1039/b406280a

Cite this

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

abstract = "Wacker-type cyclization reactions provide an effective entry into the dioxabicyclo[3.2.1]octane core of the zaragozic acid analogs. [on SciFinder(R)]",

author = "Patrick Perlmutter and Walailak Selajerern and Filisaty Vounatsos",

year = "2004",

doi = "10.1039/b406280a",

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AU - Vounatsos, Filisaty

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Y1 - 2004

N2 - Wacker-type cyclization reactions provide an effective entry into the dioxabicyclo[3.2.1]octane core of the zaragozic acid analogs. [on SciFinder(R)]

AB - Wacker-type cyclization reactions provide an effective entry into the dioxabicyclo[3.2.1]octane core of the zaragozic acid analogs. [on SciFinder(R)]

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DO - 10.1039/b406280a

M3 - Article

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VL - 2

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EP - 2228

JO - Organic & Biomolecular Chemistry

JF - Organic & Biomolecular Chemistry

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