期刊
JOURNAL OF ORGANIC CHEMISTRY
卷 88, 期 18, 页码 13331-13338出版社
AMER CHEMICAL SOC
DOI: 10.1021/acs.joc.3c01145
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This paper presents the use of 7-oxa/azanorbornadienes as synthetic intermediates for the preparation of 3/4-substituted furans/pyrroles. The method involves the inverse electron demand Diels-Alder (iEDDA) cycloaddition and retro-Diels-Alder (rDA) reactions, resulting in the synthesis of beta-substituted furans/pyrroles. The study explores the application of this method in the preparation of 29 heterocycles and proposes a one-pot procedure.
The use of 7-oxa/azanorbornadienes as synthetic intermediates for the preparation of 3/4-substituted (beta-substituted) furans/ pyrroles is presented. The method lies in the inverse electron demand Diels-Alder (iEDDA) cycloaddition between a substituted heteronorbornadiene and an electron-poor tetrazine followed by spontaneous fragmentation of the resulting cycloadduct via two retro-Diels-Alder (rDA) reactions affording a beta-substituted furan/pyrrole. The scope of this tandem iEDDA/rDA/rDA reaction was explored in the preparation of 29 heterocycles. A one-pot procedure starting directly from the alkyne precursors of the heteronorbornadiene intermediates is also described.
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