sunsaary : The carboxamidomethyl esters (CAM esters) are proposed for carboxyl protection in peptide synthesis. Amino acid CAM ester derivatives were easily prepared and showed good stability in the deblocking conditions of other convaon protecting groups used in peptide synthesis. The CAn esters we
9-fluorenylmethyl esters as carboxyl protecting group
β Scribed by Horst Kessler; Rainer Siegmeier
- Publisher
- Elsevier Science
- Year
- 1983
- Tongue
- French
- Weight
- 90 KB
- Volume
- 24
- Category
- Article
- ISSN
- 0040-4039
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β¦ Synopsis
The use of 9-fluorenylmethyl esters for the protection of carboxyl groups is proposed. The advantage of this group is the selective deprotection under mild conditions using secondary amines without racemization.
Recently we got knowledge about the use of 9-fluorenylmethyl (Fm) esters for the protection of carboxyl groups'. This leads us to publish our own results in this field2 which differ in the preparation procedure of the Fm ester, whereas the cleavage conditions are similar to those reported by Bodanszky'.
π SIMILAR VOLUMES
Carboxylic acids were protected as their corresponding 3-butenyl esters. Deprotection was carried out via ozonolysis and P-elimination of the resultant 3acyloxypropanal.
## Abstract Elimination of the hydrazide group was studied with the model compounds Nβbenzoylβglycine hydrazide and NβbenzoylβLβphenylalanine hydrazide, using phosphorus oxychloride, hydrogen bromide or hydrogen chloride in acetic acid, or 60% perchloric acid. It was found that treatment of Nβbenzo
## Abstract For Abstract see ChemInform Abstract in Full Text.