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Protection of tyrosine in solid-phase peptide synthesis

✍ Scribed by Yamashiro, Donald; Li, Choh Hao

Book ID
111917339
Publisher
American Chemical Society
Year
1973
Tongue
English
Weight
299 KB
Volume
38
Category
Article
ISSN
0022-3263

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📜 SIMILAR VOLUMES

Solid phase synthesis of fully protected
Solid phase synthesis of fully protected peptide alcohols
✍ M. Mergler; F. Dick; J. Gosteli; R. Nyfeler 📂 Article 📅 1999 🏛 Elsevier Science 🌐 French ⚖ 158 KB

A mild and efticient method to obtaia fully t-&tyl type protected alcohols based on the alkylation of Fmoc amino alcohols with the "polymeric dipheayldiazomethane" 1 followed by StanQrd Fmoc solid phase synthesis is presented. The resulting pepidyl benzhydryl ethers 3 can he cleaved with 1 -2% trlfl

Solid phase synthesis of protected pepti
Solid phase synthesis of protected peptide nucleic acids
✍ Oliver Seitz 📂 Article 📅 1999 🏛 Elsevier Science 🌐 French ⚖ 234 KB

Boc/'Z-protected PNA oligomers were synthesised on solid phase. The use of the allylic HYCRON resin allowed for the application of both Boc-and Fmoc-protecting groups. Highest yields were obtained when the monomeric building block was synthesised on solid phase rather than loaded as preformed unit.

N-Tetrachlorophthaloyl (TCP) Protection
N-Tetrachlorophthaloyl (TCP) Protection for Solid-Phase Peptide Synthesis
✍ Esther Cros; Marta Planas; George Barany; Eduard Bardají 📂 Article 📅 2004 🏛 John Wiley and Sons 🌐 English ⚖ 184 KB

## Abstract The __N__‐tetrachlorophthaloyl‐(TCP‐)amino protecting group has been evaluated for use in solid‐phase peptide synthesis. The TCP group was unaffected by exposure to either piperidine or __N__,__N__‐diisopropylethylamine (DIEA), which suggests compatibility with both Fmoc and Boc solid‐p