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- W4239455850 endingPage "4135" @default.
- W4239455850 startingPage "4131" @default.
- W4239455850 abstract "Abstract Selective three‐component 1,2‐diamination of 1,3‐dienes with concurrent introduction of two orthogonally protected amino groups remains unknown despite its significant synthetic potential. We report herein that reaction of conjugated dienes with N ‐aminopyridinium salts and TMSNCS affords 1,2‐aminoisothiocyanation products in a highly chemo‐ and regio‐selective manner under mild photoredox catalytic conditions. Mechanistic studies indicate that the facile isomerization of allyl thiocyanates to allyl isothiocyanates under photocatalytic conditions is responsible for the selective formation of the observed products. The mild isomerization protocol is expected to find applications in the synthesis of allyl isothiocyanates in a broad sense." @default.
- W4239455850 created "2022-05-12" @default.
- W4239455850 creator A5034016630 @default.
- W4239455850 creator A5046225712 @default.
- W4239455850 creator A5055586375 @default.
- W4239455850 date "2020-12-23" @default.
- W4239455850 modified "2023-10-03" @default.
- W4239455850 title "Selective 1,2‐Aminoisothiocyanation of 1,3‐Dienes Under Visible‐Light Photoredox Catalysis" @default.
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- W4239455850 doi "https://doi.org/10.1002/ange.202014518" @default.
- W4239455850 hasPublicationYear "2020" @default.
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