protected The allylic handle -0-CH2-CH-CH-CH2-0-CH2-CO-has been used in the synthesis of peptide fro ments on aminomethyl polystyrene. The palladium-catalyzed hydrostannolytic cleavage il of t e peptide fragments from the resin occurs under very mild conditions.
Enzymatic removal of acyl protecting groups. The use of dihydrocinnamoyl group in oligonucleotide synthesis and its cleavage by α-chymotrypsin
✍ Scribed by H.S. Sachdev; N.A. Starkovsky
- Publisher
- Elsevier Science
- Year
- 1969
- Tongue
- French
- Weight
- 204 KB
- Volume
- 10
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
✦ Synopsis
One of the major problems,in oligonucleotide synthesis is the design of suitable protecting groups for the reactive hydroxyl and amino functions of nucleosides and nucleotides.
Ideally, these protecting groups should satisfy the following conditions: 1) they should be stable under the reaction conditions; 2) they should be removable under essentially neutral conditions, and 3) they should display selectivity for the one or the other of the hydroxyl or amino functions.
📜 SIMILAR VOLUMES
Phosphate protection in the phosphotriester approach is improved by the new, versatile p-nitrophenylethyl group due to its stability in the condensation step and its clean removal by DBU and DBN respectively. Recent investigations in the field of oligonucleotide synthesis [l-4] have re-