Journal
JOURNAL OF ORGANIC CHEMISTRY
Volume 87, Issue 20, Pages 13469-13479Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acs.joc.2c01783
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Funding
- Consejo Nacional de Investigaciones Cientificas y Tecnicas (CONICET) [PUE-2016, PIP 2021-2023-1045]
- Agencia Nacional de Promocion Cientifica y Tecnologica (ANPCyT) [PICT-2017-2694, PICT-2018-4150]
- Agencia Santafesina de Ciencia, Tecnologia e Innovacion (ASACTEI) [AC-2015-00005]
- Universidad Nacional de Rosario [BIO 580, UNR-80020180300024UR]
- CNRS
- Ecole Polytechnique
- UPSaclay
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This article presents a synthetic strategy for constructing 2-cyclopentenones through acid-promoted cyclization of all-trans linearly conjugated dienones and dienals.
The acid-promoted cyclization of all-trans linearly conjugated dienones and dienals constitutes a synthetic strategy for the construction of 2-cyclopentenones.
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