Continuous Flow Synthesis of Morpholines and Oxazepanes with Silicon Amine Protocol (SLAP) Reagents and Lewis Acid Facilitated Photoredox Catalysis

Photocatalytic coupling of aldehydes and silicon amine protocol (SLAP) reagents enables the simple, scalable synthesis of substituted morpholines, oxazepanes, thiomorpholines, and thiazepanes under continuous flow conditions. Key to the success of this process is the combination of an inexpensive or...

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Published in:Organic letters 2017-09, Vol.19 (17), p.4696-4699
Main Authors: Jackl, Moritz K, Legnani, Luca, Morandi, Bill, Bode, Jeffrey W
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Language:English
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cited_by cdi_FETCH-LOGICAL-a390t-3f5ce417d118ed74d0b15678cd98ba62b4ede22291beed06a28bac7f610327c03
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creator Jackl, Moritz K
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description Photocatalytic coupling of aldehydes and silicon amine protocol (SLAP) reagents enables the simple, scalable synthesis of substituted morpholines, oxazepanes, thiomorpholines, and thiazepanes under continuous flow conditions. Key to the success of this process is the combination of an inexpensive organic photocatalyst (TPP) and a Lewis acid additive, which form an amine radical cation that is easily reduced to complete the catalytic cycle. Di- and trisubstituted SLAP reagents are formed in one step by an iron-catalyzed aminoetherification of olefins.
doi_str_mv 10.1021/acs.orglett.7b02395
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title Continuous Flow Synthesis of Morpholines and Oxazepanes with Silicon Amine Protocol (SLAP) Reagents and Lewis Acid Facilitated Photoredox Catalysis
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