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Orthogonal solid-phase synthesis ofN-glycopeptides using backbone protection to eliminate aspartimide formation

✍ Scribed by Laszlo Urge; Laszlo Otvos


Publisher
Springer Netherlands
Year
1995
Tongue
English
Weight
381 KB
Volume
1
Category
Article
ISSN
1573-3149

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✦ Synopsis


The side reaction of aspartimide formation during the activation of aspartic acid-containing peptides was eliminated by using backbone protection. The methodology was applied in the orthogonal solid-phase synthesis of N-glycopeptides.


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Solid-phase synthesis of tailed cyclic p
✍ Dominique Delforge; Marc Dieu; Edouard Delaive; Muriel Art; Barbara Gillon; Bart πŸ“‚ Article πŸ“… 1996 πŸ› Springer Netherlands 🌐 English βš– 651 KB

This paper discusses the application of a method developed for cyclic peptide synthesis using allyl-based sidechain-protecting groups to obtain a so-called tailed cyclic peptide, a cyclic peptide bearing a side-chain anchoring tail. The method used for the synthesis ofcyclo[-D-Val-Arg-Gly-Asp-Asp(-e