A Simple Four‐Step Synthesis of the Potato Alkaloid Demissidine from the Common Sapogenin Tigogenin
Year: 2023
Type: article
Abstract: A simple synthesis method of solanidane alkaloids from common steroidal sapogenins was developed. Previously described multi-step transformations of tigogenin to demissidine (8-12 steps) were shortened to four steps only. The key-step of the present synthesis was the epimerization at C25 of the lactam intermediate. Different approaches to this reaction, i. e., a classical one via enolate, and a chemoselective umpolung transformation, were thoroughly investigated. The epimerization step is unnecessary if the starting sapogenin has the same configuration at C25 as the target alkaloid because the configuration at C25 (either R or S) remains intact throughout the synthesis. Thus, the related solanidane alkaloids, 12β-hydroxy-25-epi-demissidine and 5-epi-demissidine, were synthesized in the three-step procedure with retention of configuration at this stereogenic center from rockogenin (25R-5α-sapogenin) or sarsasapogenin (25S-5β-sapogenin), respectively.
Source: Chemistry - A European Journal
Language: English
Subfield: Molecular Biology
Domain: Life Sciences
Open Access status: bronze
Award: G2116052537
OpenAlex ID: W4318693469
