Cyclocarbonylation of acyclic 1,3-dienes via their tricarbonyl iron complexes : Cyclopenten-2-ones and dicarbonyl cyclopentadienyl iron halides

doi:10.1016/S0040-4039(00)60188-0

Paper

Cyclocarbonylation of acyclic 1,3-dienes via their tricarbonyl iron complexes : Cyclopenten-2-ones and dicarbonyl cyclopentadienyl iron halides

Published Nov 24, 1992 · M. Franck-Neumann*, E. Michelotti, R. Simler

Tetrahedron Letters

Q3 SJR score

20

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0

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Abstract

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Study Snapshot

Cyclocarbonylation of 1,3-dienes can produce cyclopentenones under mild conditions, with 1,1,3-trialkylbutadiene complexes converting nearly quantitatively into cyclopentenones at room temperature.

PopulationOlder adults (50-71 years)

Sample size24

MethodsObservational

OutcomesBody Mass Index projections

ResultsSocial networks mitigate obesity in older groups.

Cyclocarbonylation of acyclic 1,3-dienes via their tricarbonyl iron complexes : Cyclopenten-2-ones and dicarbonyl cyclopentadienyl iron halides

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