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Nitroselenation of conjugated dienes: Preparation of 3,4-epoxy-3-nitro-1-alkenes
Uppsala University, Disciplinary Domain of Science and Technology, Chemistry, Department of Biochemistry and Organic Chemistry, Organic Chemistry.
Uppsala University, Disciplinary Domain of Science and Technology, Chemistry, Department of Biochemistry and Organic Chemistry, Organic Chemistry.
Uppsala University, Disciplinary Domain of Science and Technology, Chemistry, Department of Biochemistry and Organic Chemistry, Organic Chemistry.
Uppsala University, Disciplinary Domain of Science and Technology, Chemistry, Department of Biochemistry and Organic Chemistry, Organic Chemistry I.
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1990 (English)In: Tetrahedron Letters, ISSN 0040-4039, E-ISSN 1359-8562, Vol. 31, no 29, 4199-4202 p.Article in journal (Refereed) Published
Abstract [en]

Conjugated dienes were transformed to synthetically useful 3,4-epoxy-3-nitro-1-alkenes via a nitroselenation-oxidation sequence.

Conjugated dienes were transformed to synthetically useful 3,4-epoxy-3-nitroalkenes via a nitroselenation-oxidation sequence.

Place, publisher, year, edition, pages
1990. Vol. 31, no 29, 4199-4202 p.
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Natural Sciences
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URN: urn:nbn:se:uu:diva-140731DOI: 10.1016/S0040-4039(00)97581-6OAI: oai:DiVA.org:uu-140731DiVA: diva2:384268
Available from: 2011-01-08 Created: 2011-01-08 Last updated: 2017-12-11Bibliographically approved

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Gogoll, Adolf

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