Mild Reductive Functionalization of Amides into N ‐Sulfonylformamidines

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Location: Deutsche Nationalbibliothek Frankfurt am Main

Extent: Online-Ressource

Language: Englisch

Bibliographic citation: Mild Reductive Functionalization of Amides into N ‐Sulfonylformamidines ; volume:6 ; number:4 ; year:2017 ; pages:484-487 ; extent:4
ChemistryOpen ; 6, Heft 4 (2017), 484-487 (gesamt 4)

Creator: Trillo, Paz
Slagbrand, Tove
Tinnis, Fredrik
Adolfsson, Hans

DOI: 10.1002/open.201700087

URN: urn:nbn:de:101:1-2022100607272525429305

Rights: Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 15.08.2025, 7:27 AM CEST

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Trillo, Paz
Slagbrand, Tove
Tinnis, Fredrik
Adolfsson, Hans

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Mild Reductive Functionalization of Amides into N ‐Sulfonylformamidines

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Other Objects (12)

General α‐Amino 1,3,4‐Oxadiazole Synthesis via Late‐Stage Reductive Functionalization of Tertiary Amides and Lactams **

General α‐Amino 1,3,4‐Oxadiazole Synthesis via Late‐Stage Reductive Functionalization of Tertiary Amides and Lactams **

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General α‐Amino 1,3,4‐Oxadiazole Synthesis via Late‐Stage Reductive Functionalization of Tertiary Amides and Lactams **

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Iridium-catalyzed reductive Ugi-type reactions of tertiary amides

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Lattice Opening upon Bulk Reductive Covalent Functionalization of Black Phosphorus

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