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

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

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

April | 2011 | New Reactions
April | 2011 | New Reactions

The 3-Membered Ring In Alkene Halogenation, Oxymercuration & More
The 3-Membered Ring In Alkene Halogenation, Oxymercuration & More

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

Organic Syntheses Procedure
Organic Syntheses Procedure

N-Iodosuccinimide (NIS)
N-Iodosuccinimide (NIS)

NIS from NCS/NaI: Synthesis of alpha-Iodo Carbonyl Compounds and  trans-1,2-Iodoacetates - [www.rhodium.ws]
NIS from NCS/NaI: Synthesis of alpha-Iodo Carbonyl Compounds and trans-1,2-Iodoacetates - [www.rhodium.ws]

N-Iodosuccinimide (NIS)
N-Iodosuccinimide (NIS)

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

Iodination [Synthetic Reagents] | Tokyo Chemical Industry Co., Ltd.(APAC)
Iodination [Synthetic Reagents] | Tokyo Chemical Industry Co., Ltd.(APAC)

N-Iodosuccinimide (NIS)
N-Iodosuccinimide (NIS)

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

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

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

N-Iodosuccinimide
N-Iodosuccinimide

Organic Syntheses Procedure
Organic Syntheses Procedure

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

Azidoblebbistatin, a photoreactive myosin inhibitor | PNAS
Azidoblebbistatin, a photoreactive myosin inhibitor | PNAS

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

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

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
Photoinduced cyclization of alkynoates to coumarins with N-Iodosuccinimide as a free-radical initiator under ambient and metal-free conditions - ScienceDirect