Backbone modified oligonucleotide analogs and solid phase synthesis thereof
US5541307A · kind A · utility
550Cited by
6References
32Claims
0Family size
Assignee
Inventors
Key dates
| Filing date | Dec 28, 1993 |
| Grant date | Jul 30, 1996 |
| Priority date | — |
| Expiry date | Dec 28, 2013 |
Classification
- Technology area (CPC C)Chemistry; Metallurgy
- CPC primaryC07H19/16
- WIPO fieldPharmaceuticals
- WIPO sectorChemistry
Abstract
Compounds and methods for preparing oligonucleotide analogs are provided. In preferred embodiments, the methods involve solid-phase coupling of synthons bearing either 3'-electrophillic groups and 5'-nucleophilic groups or 5'-electrophillic groups and 3'-nucleophilic groups to form neutral, achiral oligomers.
Source: USPTO / EPO open patent data. Objective bibliographic and citation counts.