EventsThe 3rd International Electronic Conference on Synthetic Organic Chemistry
Published
This submission belongs to the session a. General Organic Synthesis of the event The 3rd International Electronic Conference on Synthetic Organic Chemistry
Published date
01 Nov, 1999
Citation
Matthias Lormann, Stefan Dahmen, Stefan Bräse, The T1 Linker: Multidirectional Cleavage for Solid Phase Organic Synthesis., in Proceedings of The 3rd International Electronic Conference on Synthetic Organic Chemistry, 1 November–30 November 1999, MDPI: Basel, Switzerland, doi: 10.3390/ecsoc-3-01724
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The T1 Linker: Multidirectional Cleavage for Solid Phase Organic Synthesis.

Stefan Bräse 1
Stefan Dahmen 1
Matthias Lormann 1
1. RWTH Aachen, Institut für Organische Chemie, Professor-Pirlet-Str. 1, D-52074 Aachen, Germany
Abstract
The T1 linker for the attachment of arenes has been described. Various transformations yielded modified arenes. The cleavage from the resin has been conducted to give hydrocarbons ("Traceless linker"), heterocycles (Richter reaction), arylated, alkenylated and alkylated arenes (Heck cleavage protocol), haloarenes, phenols, biaryls and azo compounds. This method is applicable to parallel synthesis and automation.
Keywords
n/a
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