Einfach zu passieren schwingen Privilegiert n iodosuccinimide iodination mechanism Reiben Penny Disziplin
Scandium triflate-catalyzed 6,6′-diiodination of 2,2′-dimethoxy-1,1′-binaphthyl with 1,3-diiodo-5,5-dimethylhydantoin - ScienceDirect
Sunlight-promoted cyclization versus decarboxylation in the reaction of alkynoates with N -iodosuccinimide: easy access to 3-iodocoumarins - Green Chemistry (RSC Publishing) DOI:10.1039/C6GC01027J
N-Iodosuccinimide (NIS)
Catalysts | Free Full-Text | N-Iodosuccinimide as a Precatalyst for Direct Cross-Coupling of Alcohols with C-Nucleophiles under Solvent-Free Reaction Conditions | HTML
Iodination of industrially important aromatic compounds using N- iodosuccinimide by grinding method
N-Iodosuccinimide
N-Iodosuccinimide - Wikipedia
Organic Syntheses Procedure
PDF] Mild and regioselective iodination of electron-rich aromatics with N- iodosuccinimide and catalytic trifluoroacetic acid | Semantic Scholar
Sunlight-promoted cyclization versus decarboxylation in the reaction of alkynoates with N -iodosuccinimide: easy access to 3-iodocoumarins - Green Chemistry (RSC Publishing) DOI:10.1039/C6GC01027J
Efficient synthesis of 1-iodoalkynes via Al 2 O 3 mediated reaction of terminal alkynes and N -iodosuccinimide - RSC Advances (RSC Publishing) DOI:10.1039/D0RA00251H
Iodination Using N-Iodosuccinimide (NIS)
N‐Iodosuccinimide (NIS) in Direct Aromatic Iodination - Bergström - 2017 - European Journal of Organic Chemistry - Wiley Online Library
N‐Iodosuccinimide (NIS) in Direct Aromatic Iodination - Bergström - 2017 - European Journal of Organic Chemistry - Wiley Online Library
Photoinduced cyclization of alkynoates to coumarins with N-Iodosuccinimide as a free-radical initiator under ambient and metal-free conditions - ScienceDirect
Azidoblebbistatin, a photoreactive myosin inhibitor | PNAS
N-Iodosuccinimide
Regioselective Halogenation of 1,4-Benzodiazepinones via CH Activation | Scientific Reports