Unexpected Behavior of the Heaviest Halogen Astatine in the Nucleophilic Substitution of Aryliodonium Salts-Reference-Cited by-同舟云学术

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Unexpected Behavior of the Heaviest Halogen Astatine in the Nucleophilic Substitution of Aryliodonium Salts

Published:2016-06-15 Issue:35 Volume:22 Page:12332-12339
ISSN:0947-6539
Container-title:Chemistry - A European Journal
language:en
Short-container-title:Chem. Eur. J.

Author:

Guérard François¹²^ORCID,Lee Yong-Sok³,Baidoo Kwamena¹,Gestin Jean-François²,Brechbiel Martin W.¹

Affiliation:

1. Radioimmune & Inorganic Chemistry Section; Radiation Oncology Branch; National Cancer Institute; National Institutes of Health; Bethesda Maryland 20892 USA

2. Inserm U892; CNRS UMR6299; Université de Nantes; Nantes France

3. Center for Molecular Modeling, Division of Computational Bioscience; Center for Information Technology; National Institutes of Health; Bethesda Maryland 20892 USA

Funder

National Institutes of Health

National Cancer Institute

French National Agency for Research

Publisher

Wiley

Subject

General Chemistry,Catalysis,Organic Chemistry

Reference50 articles.

1. Diaryliodonium Salts: A Journey from Obscurity to Fame

2. Diaryliodoniumsalze - aus dem Nichts ins Rampenlicht

3. Chemistry of Polyvalent Iodine

4. Diaryliodonium Salts. IV. Ion Pairs and Copper Catalysis in the Reactions of Diphenyliodonium Ions with Halide Ions and Hydroxylic Solvents.

5. Diaryliodonium Salts. VIII. Decomposition of Substituted Diphenyliodonium Halides in Inert Solvents1,2

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