Ferrer E, Wiersma M, Kazimierczak B, Müller C W, Eritja R
European Molecular Biology Laboratory, Heidelberg, Germany.
Bioconjug Chem. 1997 Sep-Oct;8(5):757-61. doi: 10.1021/bc970042l.
The behavior of oligonucleotides containing 5-iodouracil, 5-bromocytidine, and 5-iodocytidine in concentrated ammonia is described. 5-Aminouracil and 5-aminocytidine are obtained as side products when deprotection is performed at 60 degrees C. Small amounts, if any, of side products are obtained when ammonia deprotection is performed at room temperature. The base-pairing properties of these 5-halopyrimidines including triple helix are described.
描述了含有5-碘尿嘧啶、5-溴胞苷和5-碘胞苷的寡核苷酸在浓氨中的行为。当在60℃进行脱保护时,会得到5-氨基尿嘧啶和5-氨基胞苷作为副产物。在室温下进行氨脱保护时,若有副产物,其产量也很少。描述了这些5-卤代嘧啶的碱基配对特性,包括三链螺旋。