Bicatalytic Multistep Reactions En Route to the One-Pot Total Synthesis of Complex Molecules: Easy Access to Chromene and 1,2-Dihydroquinoline Derivatives from Simple Substrates

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• 作者：Pascal D. Giorgi ; Dr. Peter J. Miedziak ; Dr. Jennifer K. Edwards ; Prof. Dr. Graham J. Hutchings and Dr. Sylvain Antoniotti
• 刊名：ChemCatChem
• 出版年：2017
• 出版时间：January 9, 2017
• 年：2017
• 卷：9
• 期：1
• 页码：70-75
• 全文大小：836K
• ISSN：1867-3899

文摘

By combining nanocatalysis with base catalysis, a novel one-pot multistep process was found for the synthesis of substituted heterocycles of biological relevance from simple substrates. The process is based on the initial Au/O₂ oxidation of allylic alcohols, which is followed by base-catalyzed tandem hetero-Michael/aldolization/crotonization with ortho-hydroxy- or ortho-aminobenzaldehydes. The flexibility of the reaction even allowed the benzaldehyde partner to be prepared in situ in an example of a one-pot/five-step process.