April | 2011 | New Reactions
Azidoblebbistatin, a photoreactive myosin inhibitor | PNAS
Scheme 1. Regioselective iodination of 4-bromoveratrole with... | Download Scientific Diagram
γ-Aluminum Oxide-Mediated Iodination of Terminal Alkynes
![PDF] Mild and regioselective iodination of electron-rich aromatics with N- iodosuccinimide and catalytic trifluoroacetic acid | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/857946e16a0a13e2aebbb7814400dc8f6bc9a574/2-Table1-1.png "PDF] Mild and regioselective iodination of electron-rich aromatics with N- iodosuccinimide and catalytic trifluoroacetic acid | Semantic Scholar")
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
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
Iodination Using N-Iodosuccinimide (NIS)
N-Iodosuccinimide (NIS)
N‐Iodosuccinimide as Bifunctional Reagent in (E)‐Selective C(sp2)−H Sulfonylation of Styrenes - Pramanik - 2019 - Asian Journal of Organic Chemistry - Wiley Online Library
N‐Iodosuccinimide (NIS) in Direct Aromatic Iodination - Bergström - 2017 - European Journal of Organic Chemistry - Wiley Online Library
BJOC - Palladium-catalyzed ortho-halogenations of acetanilides with N-halosuccinimides via direct sp2 C–H bond activation in ball mills
N-Iodosuccinimide
Catalysts | Free Full-Text | N-Iodosuccinimide as a Precatalyst for Direct Cross-Coupling of Alcohols with C-Nucleophiles under Solvent-Free Reaction Conditions | HTML
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 deactivated aromatic compounds with N-iodosuccinimide in... | Download Table
Regioselective Halogenation of 1,4-Benzodiazepinones via CH Activation | Scientific Reports
Organic Syntheses Procedure
N-Iodosuccinimide (NIS)
Organic Syntheses Procedure
![Iodination [Synthetic Reagents] | Tokyo Chemical Industry Co., Ltd.(APAC)](https://www.tcichemicals.com/assets/cms-images/01047.png "Iodination [Synthetic Reagents] | Tokyo Chemical Industry Co., Ltd.(APAC)")
Iodination [Synthetic Reagents] | Tokyo Chemical Industry Co., Ltd.(APAC)
![PDF] Highly Regioselective Iodination of Arenes via Iron(III)-Catalyzed Activation of N-Iodosuccinimide. | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/0c6f0edeacfadccc931009ae2c66114570d95279/2-Table2-1.png "PDF] Highly Regioselective Iodination of Arenes via Iron(III)-Catalyzed Activation of N-Iodosuccinimide. | Semantic Scholar")
PDF] Highly Regioselective Iodination of Arenes via Iron(III)-Catalyzed Activation of N-Iodosuccinimide. | Semantic Scholar
N-Iodosuccinimide (NIS)
Selective C–H Iodination of (Hetero)arenes - ScienceDirect
N-Iodosuccinimide (NIS)
