2 article(s) from Eller, Steffen
Solid-phase synthesis of biopolymers. X represents a reactive site such as an amino group for pepti...
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Different resins used for solid-phase synthesis. (A) Hydrophobic PS resins. (B) Water-compatible re...
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Design of linker 1. Cleavage by hydrogenolysis from a solid support reveals a conjugation site for ...
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Synthesis of linker 1. Reactions and conditions: (a) NEt3, DCM, rt, 84%; (b) DHP, pyridinium p-tolu...
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Coupling of linker 1 to different resins. Reactions and conditions: (a) 1. 1 and 16 or 17, Cs2CO3, ...
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Model glycosylation by using an automated oligosaccharide synthesizer. Reactions and conditions: (a...
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Representative HPLC chromatograms of glycosylation experiments on PS-based and water-compatible res...
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Glycosylation of 34 to linker 23 and subsequent Staudinger reduction of the azide. Reactions and co...
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Beilstein J. Org. Chem. 2013, 9, 97–105, doi:10.3762/bjoc.9.13
Structures of two novel linkers on different resins.
Synthesis of a new acylsulfonamide safety-catch linker. Reagents and conditions: (a) benzaldehyde, ...
Functionalization of different resins. Reagents and conditions: (a) Cs2CO3, DMF, TBAI, Merrifield c...
Glycosylation and cleavage reactions for analysis. Reagents and conditions: (a) automated glycosyla...
Further investigations of safety-catch linker. Reagents and conditions: (a) NaOMe, MeOH; (b) 19, NI...
Beilstein J. Org. Chem. 2012, 8, 2067–2071, doi:10.3762/bjoc.8.232
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