Protection of carboxamide functions by the trityl residue. Application to peptide synthesis
β Scribed by Peter Sieber; Bernhard Riniker
- Publisher
- Elsevier Science
- Year
- 1991
- Tongue
- French
- Weight
- 341 KB
- Volume
- 32
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
β¦ Synopsis
Carboxamlde fun&Ions may be tntylated by an aad-catalyzed reaction wth tnphenylmethanol and acetic anhydnde m glaaal acetic acid The w-tntyl group of asparagme and glutamme 1s cleavable by TFA, but stable to strong rnmeral aads m aqueous solution, as well as to nucleophlles and bases In pepbde syntheses, It 1s Ideally sulted for combmatlon with slde-cham protectlons of the t butyl-type
π SIMILAR VOLUMES
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a βFull Textβ option. The original article is trackable v
The picolinoyl group can be used as a convenient protective group for amines in peptide chemistry. Deprotection is performed by electrochemical reduction under mild acidic conditions.
## Abstract The 4βmethoxybenzyl thioether protecting group is deblocked efficiently by oxidation with the homogeneous electron transfer agent tris(4βbromophenyl)ammoniumyl (**2**^.β^) leading to the disulfide in high yields. __S__β(4βmethoxybenzyl)cysteine derivatives like **9** in this way can be