期刊:Synlett [Thieme Medical Publishers (Germany)] 日期:2024-06-24
标识
DOI:10.1055/a-2351-4828
摘要
Abstract We report a practical scalable synthesis of the natural product (±)-tylophorine by using an operationally simple protecting-group-free route from readily accessible starting materials. Synthesis of a cyclic N-acetyl diester compound through cyclization, followed by two key steps (decarboxylation and a Clemmensen reduction), provides access to the target molecule.