Light-fluorous safety-catch arylgermanes ? exceptionally robust, photochemically activated precursors for biaryl synthesis by Pd(0) catalysed cross-coupling-Reference-Cited by-同舟云学术

Light-fluorous safety-catch arylgermanes ? exceptionally robust, photochemically activated precursors for biaryl synthesis by Pd(0) catalysed cross-coupling

Published:2007 Issue:28 Volume: Page:2926
ISSN:1359-7345
Container-title:Chemical Communications
language:en
Short-container-title:Chem. Commun.

Author:

Spivey Alan C.,Tseng Chih-Chung,Hannah Joseph P.,Gripton Christopher J. G.,de Fraine Paul,Parr Nigel J.,Scicinski Jan J.

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,Metals and Alloys,Surfaces, Coatings and Films,General Chemistry,Ceramics and Composites,Electronic, Optical and Magnetic Materials,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2007/CC/B707517K

Reference23 articles.

1. The Combinatorial Synthesis of Bicyclic Privileged Structures or Privileged Substructures

2. Aryl−Aryl Bond Formation One Century after the Discovery of the Ullmann Reaction

3. Diversity Linker Units for Solid‐Phase Organic Synthesis

4. A novel solid-phase equivalent to the triflate group and its application to traceless linking and cross-coupling-release strategiesElectronic Supplementary Information (ESI) available: typical experimental procedures and data for preparation of polymers and subsequent cleavage. See http://www.rsc.org/suppdata/cc/b4/b408021a/

5. A ‘triflate-like’ tetrafluoroarylsulfonate linker for multifunctional solid-phase organic synthesis

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