๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

New C-protective group for peptide synthesis

โœ Scribed by MUTULIS, F. ;MUTULE, I. ;BALODIS, J. ;SEKACIS, I. ;BRIVKALNE, L. ;IPENS, G.


Book ID
115099450
Publisher
Wiley (Blackwell Publishing)
Year
2009
Tongue
English
Weight
598 KB
Volume
42
Category
Article
ISSN
0367-8377

No coin nor oath required. For personal study only.


๐Ÿ“œ SIMILAR VOLUMES


New protective groups for peptide synthe
โœ D.S. Kemp; David C. Roberts ๐Ÿ“‚ Article ๐Ÿ“… 1975 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 261 KB

Prutecting groups which permit modification of solubility properties of peptide derivatives or which can act as "handles",1 allowing isolation by selective affinity, offer great potential for facilitating the manipulations of peptide chemistry."2 We report preparation and properties of p-dihydroxybo

Acetol: a useful new protecting group fo
โœ Bijoy Kundu ๐Ÿ“‚ Article ๐Ÿ“… 1992 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 152 KB

Acetol can be conveniently used as a reagent for the protection of carboxylic acids in peptide synthesis. It has been found to be inert and stable to hydrogenolytic and acidolytic conditions normally used in peptide synthesis. Deblocking has been selectively achieved under mild conditions using Bu4N

(p-Phenylazophenyl)-Isopropyloxycarbonyl
โœ Aung Tun-Kyi; Robert Schwyzer ๐Ÿ“‚ Article ๐Ÿ“… 1976 ๐Ÿ› John Wiley and Sons ๐ŸŒ German โš– 267 KB

## Abstract The preparation and properties of thirty two N(ฮฑ)โ€[2โ€(__p__โ€phenylazophenyl)โ€isopropylcarbonyl]โ€aminoโ€acids and derivatives are described. The new coloured protecting group (AZOCโ€) can be easily and selectively removed with mild acid treatment, much the same as the 2โ€(biphenyl)โ€isopropy

Protecting Groups for the Enzymatic Pept
โœ A. FLร–RSHEIMER; A. SCHWARZ; D. STEINKE; M. KITTELMANN; G. HERRMANN; M. R. KULA; ๐Ÿ“‚ Article ๐Ÿ“… 1990 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 178 KB