Flexible Stereo- and Regioselective Synthesis of myo-Inositol Phosphates (Part 2): Via Nonsymmetrical Conduritol B Derivatives

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  • Bergische Universität Wuppertal
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OriginalspracheEnglisch
Seiten (von - bis)3116-3127
Seitenumfang12
FachzeitschriftEuropean Journal of Organic Chemistry
Jahrgang2005
Ausgabenummer14
PublikationsstatusVeröffentlicht - 4 Juli 2005
Extern publiziertJa

Abstract

A practical route is described for the preparation of myo-inositol phosphates. Optically pure compounds can be prepared, in both forms, from p-benzoquinone by enzymatic resolution of a diacetoxyconduritol key intermediate. Monosubstituted inositol derivatives can be obtained by breaking the C2 symmetry of conduritol B derivatives. A wide variety of myo-inositol phosphates can be synthesized by combining the previously reported symmetrical approach with this new non-symmetrical approach.

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Flexible Stereo- and Regioselective Synthesis of myo-Inositol Phosphates (Part 2): Via Nonsymmetrical Conduritol B Derivatives. / Podeschwa, Michael A.L.; Plettenburg, Oliver; Altenbach, Hans Josef.
in: European Journal of Organic Chemistry, Jahrgang 2005, Nr. 14, 04.07.2005, S. 3116-3127.

Publikation: Beitrag in FachzeitschriftArtikelForschungPeer-Review

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T1 - Flexible Stereo- and Regioselective Synthesis of myo-Inositol Phosphates (Part 2)

T2 - Via Nonsymmetrical Conduritol B Derivatives

AU - Podeschwa, Michael A.L.

AU - Plettenburg, Oliver

AU - Altenbach, Hans Josef

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KW - Asymmetric synthesis

KW - Biocatalytic resolution

KW - Inositol phosphates

KW - Natural products

KW - Phosphorylation

KW - Protecting groups

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JO - European Journal of Organic Chemistry

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