Yousefi-Salakdeh Esmail, Murtola Merita, Zetterberg Anders, Yeheskiely Esther, Strömberg Roger
Division of Organic and Bioorganic Chemistry, MBB, Scheele Laboratory, Karolinska Institutet, S-17177 Stockholm, Sweden.
Bioorg Med Chem. 2006 Apr 15;14(8):2653-9. doi: 10.1016/j.bmc.2005.11.049. Epub 2005 Dec 20.
A short and efficient route for the synthesis of aminoalkyl 8-aminoadenylates, potential aminoacyl-tRNA synthetase inhibitors, is presented. Aminoalkyl 8-aminoadenylates were synthesized using a 5'-H-phosphonate strategy involving minimal protecting group manipulations and a single final deprotection step.
本文介绍了一种合成氨基烷基8-氨基腺苷酸酯(潜在的氨酰-tRNA合成酶抑制剂)的简短而高效的路线。氨基烷基8-氨基腺苷酸酯是采用5'-H-膦酸酯策略合成的,该策略涉及最少的保护基操作和单一的最终脱保护步骤。