Details
Original language | English |
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Pages (from-to) | 999-1000 |
Number of pages | 2 |
Journal | Journal of the Chemical Society, Chemical Communications |
Issue number | 8 |
Publication status | Published - 1994 |
Externally published | Yes |
Abstract
Tricarbonyl(η6-1,2-dioxobenzocyclobutene)chromium(0) 1 can be converted into benzocyclooctenedione derivatives 3, 7 and 8 as well as fused five-membered ring systems 2, 4 and 6 by addition of vinyl lithium derivatives and following double anionic oxy-Cope rearrangement under very mild reaction conditions (-78 °C); product ratios depend on the method of hydrolysis.
ASJC Scopus subject areas
- Biochemistry, Genetics and Molecular Biology(all)
- Molecular Medicine
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In: Journal of the Chemical Society, Chemical Communications, No. 8, 1994, p. 999-1000.
Research output: Contribution to journal › Article › Research › peer review
}
TY - JOUR
T1 - Syntheses of Benzocyclooctenedione Derivatives, Cyclopenta[a]indanones and a Benzo-anellated Tetraquinane via Sequential Transformations of Tricarbonyl(η6-1,2-dioxobenzocyclobutene)chromium(0)
AU - Brands, Michael
AU - Bruckmann, Joachim
AU - Krüger, Carl
AU - Butenschön, Holger
PY - 1994
Y1 - 1994
N2 - Tricarbonyl(η6-1,2-dioxobenzocyclobutene)chromium(0) 1 can be converted into benzocyclooctenedione derivatives 3, 7 and 8 as well as fused five-membered ring systems 2, 4 and 6 by addition of vinyl lithium derivatives and following double anionic oxy-Cope rearrangement under very mild reaction conditions (-78 °C); product ratios depend on the method of hydrolysis.
AB - Tricarbonyl(η6-1,2-dioxobenzocyclobutene)chromium(0) 1 can be converted into benzocyclooctenedione derivatives 3, 7 and 8 as well as fused five-membered ring systems 2, 4 and 6 by addition of vinyl lithium derivatives and following double anionic oxy-Cope rearrangement under very mild reaction conditions (-78 °C); product ratios depend on the method of hydrolysis.
UR - http://www.scopus.com/inward/record.url?scp=37049067780&partnerID=8YFLogxK
U2 - 10.1039/C39940000999
DO - 10.1039/C39940000999
M3 - Article
AN - SCOPUS:37049067780
SP - 999
EP - 1000
JO - Journal of the Chemical Society, Chemical Communications
JF - Journal of the Chemical Society, Chemical Communications
SN - 0022-4936
IS - 8
ER -