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Synthesis of NovelN-substituted guanidine linked nucleoside dimers and their incorporation into oligonucleotides

Authors
Journal
Bioorganic & Medicinal Chemistry Letters
0960-894X
Publisher
Elsevier
Publication Date
Volume
3
Issue
2
Identifiers
DOI: 10.1016/s0960-894x(01)80875-1

Abstract

Abstract Dimer building blocks (5a-j) with an N substituted guanideine function were prepared by reaction of 5'-amino-5'-deoxythymidine (1) with S,S -dimethyl- N substituted iminodithicarbonimidates (2a-j) followed by reaction of the isothiourea (3a-j) with 3'-amino-3'-deoxythymidine (4). All dimers were protected at the primary hydroxyl group with dimethoxytrityl group, converted to the phosphoramidite building blocks and incorporated into DNA.

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