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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
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
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
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 (NIS)

N-Iodosuccinimide
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
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
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
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
N-Iodosuccinimide

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

Photo-mediated selective deconstructive geminal dihalogenation of  trisubstituted alkenes | Nature Communications
Photo-mediated selective deconstructive geminal dihalogenation of trisubstituted alkenes | Nature Communications

Organic Syntheses Procedure
Organic Syntheses Procedure

Arene C–H Iodination Using Aryl Iodides
Arene C–H Iodination Using Aryl Iodides

Regioselective Halogenation of 1,4-Benzodiazepinones via CH Activation |  Scientific Reports
Regioselective Halogenation of 1,4-Benzodiazepinones via CH Activation | Scientific Reports

N-Iodosuccinimide - Wikipedia
N-Iodosuccinimide - Wikipedia

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

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

N-Iodosuccinimide-Promoted Cascade Trifunctionalization of Alkynoates:  Access to 1,1-Diiodoalkenes | Organic Letters
N-Iodosuccinimide-Promoted Cascade Trifunctionalization of Alkynoates: Access to 1,1-Diiodoalkenes | Organic Letters

Iodination of industrially important aromatic compounds using N- iodosuccinimide by grinding method
Iodination of industrially important aromatic compounds using N- iodosuccinimide by grinding method

Iodination Using N-Iodosuccinimide (NIS)
Iodination Using N-Iodosuccinimide (NIS)

Iodination of deactivated aromatic compounds with N-iodosuccinimide in... |  Download Table
Iodination of deactivated aromatic compounds with N-iodosuccinimide in... | Download Table

γ-Aluminum Oxide-Mediated Iodination of Terminal Alkynes
γ-Aluminum Oxide-Mediated Iodination of Terminal Alkynes

Iodination of industrially important aromatic compounds using N- iodosuccinimide by grinding method
Iodination of industrially important aromatic compounds using N- iodosuccinimide by grinding method

Scheme 1. Regioselective iodination of 4-bromoveratrole with... | Download  Scientific Diagram
Scheme 1. Regioselective iodination of 4-bromoveratrole with... | Download Scientific Diagram

Organic Syntheses Procedure
Organic Syntheses Procedure

Scandium triflate-catalyzed 6,6′-diiodination of  2,2′-dimethoxy-1,1′-binaphthyl with 1,3-diiodo-5,5-dimethylhydantoin -  ScienceDirect
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
Catalysts | Free Full-Text | N-Iodosuccinimide as a Precatalyst for Direct Cross-Coupling of Alcohols with C-Nucleophiles under Solvent-Free Reaction Conditions | HTML