Use of the hexafluoro-2-butyl protecting group in the synthesis of DNA fragments via the phosphoramidite approach on solid supports
β Scribed by Sung-Gug Kim; Kouichi Eida; Hiroshi Takaku
- Publisher
- Elsevier Science
- Year
- 1995
- Tongue
- English
- Weight
- 210 KB
- Volume
- 5
- Category
- Article
- ISSN
- 0960-894X
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β¦ Synopsis
The hexafluoro-2-butyl (HFB) group is a new protecting group for internucleotidic bonds in the synthesis of oligodeoxydbonuclootides by the phosphoramidite approach. This group can be removed rapidly under the same condition as the 2--eyanoethyl group. Furthermore, we have found that the phosphitylating agent, hexafluoro-2-butyl-N.N-dialkylaminochlorophosphine, is easy to prepare in terms of its stability during purification by distillation, which does not require high vacuum.
π SIMILAR VOLUMES
The development of the 2-(4-trifluoromethylphenylsulfonyl)ethoxycarbonyl (Tsc) function, a novel base-sensitive amino-protecting group, and its application to the preparation of DNA-binding polyamides are described. Pyrrole-imidazole polyamides were synthesized by an efficient solid-phase method und
The new base labile CPSEC group has been successfully employed for the protection of the 5'-hydroxyl function to synthesize a "universal Stop codon" DNA sequence: 5'd(TCAATCAATCA)3'.
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.