| Literature DB >> 26845521 |
Yuki Matsuno1, Takao Shoji1, Shokaku Kim1, Kazuhiro Chiba1.
Abstract
A straightforward method for the synthesis of oligonucleotide blocks using a Cbz-type alkyl-chain-soluble support (Z-ACSS) attached to the 3'-OH group of 3'-terminal nucleosides was developed. The Z-ACSS allowed for the preparation of fully protected deoxyribo- and ribo-oligonucleotides without chromatographic purification and released dimer- to tetramer-size oligonucleotide blocks via hydrogenation using a Pd/C catalyst without significant loss or migration of protective groups such as 5'-end 4,4'-dimethoxtrityl, 2-cyanoethyl on internucleotide bonds, or 2'-TBS.Entities:
Mesh:
Substances:
Year: 2016 PMID: 26845521 DOI: 10.1021/acs.orglett.6b00077
Source DB: PubMed Journal: Org Lett ISSN: 1523-7052 Impact factor: 6.005