Alkyl- and Arylthiodediazoniations of Dry Arenediazonium o-Benzenedisulfonimides. Efficient and Safe Modifications of the Stadler and Ziegler Reactions to Prepare Alkyl Aryl and Diaryl Sulfides-Reference-Cited by-同舟云学术

Alkyl- and Arylthiodediazoniations of Dry Arenediazonium o-Benzenedisulfonimides. Efficient and Safe Modifications of the Stadler and Ziegler Reactions to Prepare Alkyl Aryl and Diaryl Sulfides

Published:2000-08-17 Issue:18 Volume:65 Page:5600-5608
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Barbero Margherita¹,Degani Iacopo¹,Diulgheroff Nicola¹,Dughera Stefano¹,Fochi Rita¹,Migliaccio Mara¹

Affiliation:

1. Dip.to di Chimica Generale ed Organica Applicata dell'Università, C.so M. D'Azeglio 48, I-10125 Torino, Italy

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo0003347

Reference44 articles.

1. New Dry Arenediazonium Salts, Stabilized to an Exceptionally High Degree by the Anion of o-Benzenedisulfonimide

2. Preparation of Diazenes by Electrophilic C-Coupling Reactions of Dry Arenediazonium o-Benzenedisulfonimides with Grignard Reagents

3. A Simple Preparation of Aryl Methanesulfonates by Thermal Decomposition of Dry Arenediazonium o-Benzenedisulfonimides in Methanesulfonic Acid

4. Halodediazoniations of Dry Arenediazonium o-Benzenedisulfonimides in the Presence or Absence of an Electron Transfer Catalyst. Easy General Procedures To Prepare Aryl Chlorides, Bromides, and Iodides

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