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Versatile Dde-based primary amine linkers for solid phase synthesis

✍ Scribed by Siri Ram Chhabra; Azra N. Khan; Barrie W. Bycroft


Publisher
Elsevier Science
Year
1998
Tongue
French
Weight
253 KB
Volume
39
Category
Article
ISSN
0040-4039

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πŸ“œ SIMILAR VOLUMES


A Dde-based carboxy linker for solid-pha
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The Dde-derived carboxy protecting group, 4-{N-[1-(4,4-dimethyl-2,6-dioxocyclohexylidene)-3-methylbutyl]amino}benzyl ester (ODmab) has been developed into a carboxy functional linker. The stability of the linker to standard acid and base conditions employed in Fmoc/tBu SPPS has been demonstrated and

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A novel linker for the solid-phase synthesis of secondary amines based on an intramolecular cyclization was developed. The linker allows for a stepwise built-up of the secondary amines on the support. The feasibility was demonstrated in the parallel synthesis of a small set of different secondary am

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The synthesis of 9-(4-hydroxyphenyl)-9-H-fluoren-9-ol and 5-(4-(9-hydroxy-9H-fluoren-9-yl)-phenoxy)pentanoic acid and their applications as new linkers for solid phase synthesis is reported. These supports show higher acid stability compared to standard trityl resins. Carboxylic acids and amines are

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A new and cost-effective linker for the generation of carboxylic acid end groups on Multipin supports (SynPhaseβ„’ crowns) has been developed. Synthesis of the linker was based on modification of grafted polystyrene (PS) crowns to generate a hydroxyethyl moiety which is acid labile in 10 -20% trifluor

A novel, thioacetal based linker for sol
✍ Christoph M Huwe; Hermann KΓΌnzer πŸ“‚ Article πŸ“… 1999 πŸ› Elsevier Science 🌐 French βš– 286 KB

Commercially available (+)-ct-lipoic acid was employed as a novel, chemically robust linker for the immobilization of ketones. The utility of this thioacetal based linker in solid-phase synthesis was demonstrated by synthesizing several 4-acetylbiphenyls and 4-alkoxyacetophenones via Suzuki and Mits