η 6‐(1,2‐Dioxocyclobutabenzene)tricarbonyl‐chromium(0): Starting Material for Double Anionic Oxy‐Cope Rearrangements under Very Mild Conditions

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  • Max-Planck-Institut für Kohlenforschung
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Translated title of the contributionη6-(1,2-Dioxocyclobutabenzol)tricarbonylchrom(O): Edukt für doppelt anionische Oxy-Cope-Umlagerungen unter besonders milden Bedingungen
Original languageEnglish
Pages (from-to)267-269
Number of pages3
JournalAngewandte Chemie International Edition in English
Volume32
Issue number2
Publication statusPublished - Feb 1993
Externally publishedYes

Abstract

Certainly one of the most strained arene complexes known, the title compound 1 is described here. Its reactivity is characterized by the differentiation of the sides of attack at the bicyclic ligand. On addition of alkenyl metal reagents this leads to an ideal configuration for double anionic oxy‐Cope rearrangements, providing access to benzoannelated cyclooctan‐1,4‐dione derivatives. (Figure Presented.)

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η 6‐(1,2‐Dioxocyclobutabenzene)tricarbonyl‐chromium(0): Starting Material for Double Anionic Oxy‐Cope Rearrangements under Very Mild Conditions. / Brands, Michael; Goddard, Richard; Wey, Hans G. et al.
In: Angewandte Chemie International Edition in English, Vol. 32, No. 2, 02.1993, p. 267-269.

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abstract = "Certainly one of the most strained arene complexes known, the title compound 1 is described here. Its reactivity is characterized by the differentiation of the sides of attack at the bicyclic ligand. On addition of alkenyl metal reagents this leads to an ideal configuration for double anionic oxy‐Cope rearrangements, providing access to benzoannelated cyclooctan‐1,4‐dione derivatives. (Figure Presented.)",
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T2 - Starting Material for Double Anionic Oxy‐Cope Rearrangements under Very Mild Conditions

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AU - Goddard, Richard

AU - Wey, Hans G.

AU - Butenschön, Holger

PY - 1993/2

Y1 - 1993/2

N2 - Certainly one of the most strained arene complexes known, the title compound 1 is described here. Its reactivity is characterized by the differentiation of the sides of attack at the bicyclic ligand. On addition of alkenyl metal reagents this leads to an ideal configuration for double anionic oxy‐Cope rearrangements, providing access to benzoannelated cyclooctan‐1,4‐dione derivatives. (Figure Presented.)

AB - Certainly one of the most strained arene complexes known, the title compound 1 is described here. Its reactivity is characterized by the differentiation of the sides of attack at the bicyclic ligand. On addition of alkenyl metal reagents this leads to an ideal configuration for double anionic oxy‐Cope rearrangements, providing access to benzoannelated cyclooctan‐1,4‐dione derivatives. (Figure Presented.)

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