A solid-phase synthesis of Park nucleotide as well as lipids I and II analogues, which is applicable to the synthesis of a range of analogues, is described in this work. This technique allows highly functionalized macromolecules to be modularly labeled. Multiple steps are used in a short time (4 d) with a single purification step to synthesize the molecules by solid-phase synthesis.
|ジャーナル||Chemical and Pharmaceutical Bulletin|
|出版物ステータス||Published - 2018 1 1|
ASJC Scopus subject areas
- Drug Discovery