𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Protection of the phosphoryl group in oligonucleotides in the form of a dianilidate. Dianilidophosphochloridate as phosphorylating agent

✍ Scribed by J. Smrt


Publisher
Elsevier Science
Year
1973
Tongue
French
Weight
123 KB
Volume
14
Category
Article
ISSN
0040-4039

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


Trityloxyethylamino group for the protec
✍ Toshiki Tanaka; Yasuki Yamada; Morio Ikehara πŸ“‚ Article πŸ“… 1986 πŸ› Elsevier Science 🌐 French βš– 180 KB

Trityloxyethylamino group was used for the protection of 5'-phosphoryl group of deoxyribonucleoside. This group is not only protecting group of phosphate also the intermediate for the synthesis of d-ppA and d-pppA. The synthesis of deoxyoligonucleotide with a defined sequence is accomplished very

A comparison of histidine protecting gro
✍ Maite BeltrΓ‘n; Enrique Pedroso; Anna Grandas πŸ“‚ Article πŸ“… 1998 πŸ› Elsevier Science 🌐 French βš– 278 KB

Protection of the imidazole ring of the histidine residue is not required for the elongation of an oligonucleotide chain at the side chain hydroxyl group of an amino acid residue by the phosphite triester approach. For the assembly of the peptide chain, the 2,4-dinitrophenyl group is the best altern

Taurine might be acting as a trophic fac
✍ Lucimey Lima; Suzana Cubillos πŸ“‚ Article πŸ“… 1998 πŸ› John Wiley and Sons 🌐 English βš– 223 KB

Protein phosphorylation is involved in the regeneration of the nervous system. Taurine modulates the phosphorylation of specific proteins in the retina, and also increases outgrowth from ganglion cells. In order to test the possible role of protein phosphorylation on the outgrowth from the retina an

Application of levulinic acid ester as a
✍ H. J. Koeners; J. Verhoeven; J. H. van Boom πŸ“‚ Article πŸ“… 2010 πŸ› Elsevier Science 🌐 English βš– 989 KB

## Abstract The fast, selective and mild removal of levulinoyl groups with hydrazine from galactose, which also carries hydroxyl functions protected with acetyl groups, enabled us, under Koenigs‐Knorr conditions, to synthesize tri‐ and tetrasaccharides containing β‐linked galactose and glucose unit