Strategie Anerkennung Egal ob n iodosuccinimide iodination mechanism deutlich Billy genetisch
N‐Iodosuccinimide as Bifunctional Reagent in (E)‐Selective C(sp2)−H Sulfonylation of Styrenes - Pramanik - 2019 - Asian Journal of Organic Chemistry - Wiley Online Library
Selective C–H Iodination of (Hetero)arenes - ScienceDirect
Catalysts | Free Full-Text | N-Iodosuccinimide as a Precatalyst for Direct Cross-Coupling of Alcohols with C-Nucleophiles under Solvent-Free Reaction Conditions | HTML
N-Iodosuccinimide (NIS)
N-Iodosuccinimide
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
Azidoblebbistatin, a photoreactive myosin inhibitor | PNAS
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
N-Iodosuccinimide
PDF] Highly Regioselective Iodination of Arenes via Iron(III)-Catalyzed Activation of N-Iodosuccinimide. | Semantic Scholar
Scandium triflate-catalyzed 6,6′-diiodination of 2,2′-dimethoxy-1,1′-binaphthyl with 1,3-diiodo-5,5-dimethylhydantoin - ScienceDirect
Catalysts | Free Full-Text | N-Iodosuccinimide as a Precatalyst for Direct Cross-Coupling of Alcohols with C-Nucleophiles under Solvent-Free Reaction Conditions | HTML