๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

Synthesis of oligonucleotides via phosphoramidite approach utilizing 2-diphenylmethylsilylethyl (DPSE) as a phosphorus protecting group

โœ Scribed by Vasulinga T. Ravikumar; Tadeusz K. Wyrzykiewicz; Douglas L. Cole


Publisher
Elsevier Science
Year
1994
Tongue
French
Weight
816 KB
Volume
50
Category
Article
ISSN
0040-4020

No coin nor oath required. For personal study only.

โœฆ Synopsis


Absbwct: 2-Diphenylmethylsilylethyl (DPSE) is a new protecting group for internucleotidic bonds in the synthesis of oligodeoqribo nucleotides by the phosphoramidite approach. This group is stable to acidic conditions and can be removed under mild /3$ragmentation conditions using aqueous ammonium hydroxide.


๐Ÿ“œ SIMILAR VOLUMES


Use of 2-methylsulfonylethyl as a phosph
โœ C. Claesen; G.I. Tesser; C.E. Dreef; J.E. Marugg; G.A. van der Marel; J.H. van B ๐Ÿ“‚ Article ๐Ÿ“… 1984 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 204 KB

2-Methylsulfonylethoxy dichlorophosphine has been converted into the mono-N-morpholino derivative and applied for the preparation of 5'-D,N-protected d-nucleoside-3'-phosphoramidites. The latter intermediates could be used in the presence of 1-hydroxyben~otriazole for the formation of 3'-5'-phosphot

4-Cyano-2-butenyl group: A new type of p
โœ Vasulinga T. Ravikumar; Zacharia S. Cheruvallath; Douglas L. Cole ๐Ÿ“‚ Article ๐Ÿ“… 1996 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 258 KB

4-Cyano-2-butenyl (CB) is a new type of protecting group for the intemucleotidic bonds in the synthesis of oligodeoxyribonucleotides by the phosphoramidite approach. This group is stable to acidic conditions and can be removed under mild conditions by a 8-elimination pathway using aqueous ammonium h