Acylsulfonamide safety-catch linker: promise and limitations for solid–phase oligosaccharide synthesis
Safety-catch linkers are useful for solid-phase oligosaccharide synthesis as they are orthogonal to many common protective groups. A new acylsulfonamide safety-catch linker was designed, synthesized and employed during glycosylations using an automated carbohydrate synthesizer. The analysis of the c...
Main Authors: | Jian Yin, Steffen Eller, Mayeul Collot, Peter H. Seeberger |
---|---|
Format: | Article |
Language: | English |
Published: |
Beilstein-Institut
2012-11-01
|
Series: | Beilstein Journal of Organic Chemistry |
Subjects: | |
Online Access: | https://doi.org/10.3762/bjoc.8.232 |
Similar Items
-
Glycosylation efficiencies on different solid supports using a hydrogenolysis-labile linker
by: Mayeul Collot, et al.
Published: (2013-01-01) -
Safety-Catch Linkers for Solid-Phase Peptide Synthesis
by: Sikabwe Noki, et al.
Published: (2024-03-01) -
Role for Gag-CA Interdomain Linker in Primate Lentiviral Replication
by: Naoya Doi, et al.
Published: (2019-08-01) -
Photolabile linkers for solid-phase synthesis
by: Mikkelsen, Remi J. T., et al.
Published: (2020) -
Linker, loading, and reaction scale influence automated glycan assembly
by: Marlene C. S. Dal Colle, et al.
Published: (2023-07-01)