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1,3-hydron transfer in some 5- or 7-substituted 1-methylindenes. Reaction rates and kinetic isotope effects
Uppsala University, Disciplinary Domain of Science and Technology, Chemistry, Department of Chemistry.
Uppsala University, Disciplinary Domain of Science and Technology, Chemistry, Department of Chemistry.
Uppsala University, Disciplinary Domain of Humanities and Social Sciences, Faculty of Arts, Centre for Gender Research. Uppsala University, Disciplinary Domain of Science and Technology, Chemistry, Department of Chemistry.
Uppsala University, Disciplinary Domain of Science and Technology, Chemistry, Department of Chemistry.
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1998 (English)In: Acta Chemica Scandinavica, ISSN 0904-213X, E-ISSN 1902-3103, Vol. 52, no 7, 911-920 p.911-920 p.Article in journal (Refereed) Published
Abstract [en]

Rate constants and primary deuterium kinetic isotope effects (KIEs) have been determined for the base-catalysed 1,3-hydrotropic rearrangements of 1-methyl-5-nitroindene (12), 1-methyl-7-nitroindene (13), 5-methoxy-1-methylindene (14) and 5-fluoro-1-methy

Place, publisher, year, edition, pages
MUNKSGAARD INT PUBL LTD , 1998. Vol. 52, no 7, 911-920 p.911-920 p.
Keyword [en]
CATALYZED 1;3-PROTON TRANSFER; SOLVENT DEPENDENCE; REARRANGEMENT; ELIMINATION
National Category
Organic Chemistry
Identifiers
URN: urn:nbn:se:uu:diva-84765OAI: oai:DiVA.org:uu-84765DiVA: diva2:112673
Note

Addresses: Aune M, Uppsala Univ, Inst Chem, POB 531, S-75121 Uppsala, Sweden. Uppsala Univ, Inst Chem, S-75121 Uppsala, Sweden.

Available from: 2008-10-17 Created: 2008-10-17 Last updated: 2016-05-03

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Hussenius, Anita

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