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Development of new linkers for the formation of aliphatic C-H bonds on polymeric supports

✍ Scribed by Kyung Woon Jung; Xy-yang Zhao; Kim D. Janda


Book ID
104207729
Publisher
Elsevier Science
Year
1997
Tongue
French
Weight
532 KB
Volume
53
Category
Article
ISSN
0040-4020

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✦ Synopsis


Two polymeric linkers, 8 and II, were prepared in high yields. Aftachment of an alkyl group to these linkers was facile, and their cleavage from the MeO-PEG polymer support was accomplished by desulfurization using Raney nickel to yield the new carbon-hydrogen bond product 6. The protocol reported herein allows ejjicient preparation of new polymeric linkers as well as their possible application to combinatorial libraries. 0 1997


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A new aminoethyl-polystyrene linker, stable at low concentrations of TFA, has been developed for the solid phase synthesis of peptide amides. The described linker is stable under conditions which remove Bu(t) protecting groups (30-50% TFA in DCM) and the desired product can be finally cleaved off th