Ring‐Opening of a Bicyclo[3.2.0]hepta‐1,3‐dienyl‐cobalt(I) Complex Followed by Cycloaddition

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  • Max-Planck-Institut für Kohlenforschung
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Translated title of the contributionVierringöffnung eines Bicyclo[3.2.0]hepta-1,3-dienylcobalt(I)-Komplexes mit nachfolgender Cycloaddition
Original languageEnglish
Pages (from-to)1057-1059
Number of pages3
JournalAngewandte Chemie International Edition in English
Volume29
Issue number9
Publication statusPublished - Sept 1990
Externally publishedYes
EventChemiedozenten-Tagung - Ulm, Germany
Duration: 1 Jan 1990 → …

Abstract

The four‐membered ring of the cobalt complex 1 is opened at only 200°C. The resulting allyl diene system 2 can be trapped by [2 + 4] cycloaddition with dienophiles to give cycloadducts such as 3 in good yields. The stereochemistry of the cycloadducts is strongly influenced by the coordination behavior of the dienophile. L = tetraphenylcyclobutadiene, E = COOCH3. (Figure Presented.)

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Ring‐Opening of a Bicyclo[3.2.0]hepta‐1,3‐dienyl‐cobalt(I) Complex Followed by Cycloaddition. / Butenschön, Holger.
In: Angewandte Chemie International Edition in English, Vol. 29, No. 9, 09.1990, p. 1057-1059.

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abstract = "The four‐membered ring of the cobalt complex 1 is opened at only 200°C. The resulting allyl diene system 2 can be trapped by [2 + 4] cycloaddition with dienophiles to give cycloadducts such as 3 in good yields. The stereochemistry of the cycloadducts is strongly influenced by the coordination behavior of the dienophile. L = tetraphenylcyclobutadiene, E = COOCH3. (Figure Presented.)",
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