Related Experiment Video
Updated: Aug 8, 2026

Preparation of Enantiopure Non-Activated Aziridines and Synthesis of Biemamide B, D, and epiallo-Isomuscarine
Published on: June 13, 2022
Natural products as templates for bioactive compound libraries: synthesis of biaryl derivatives of (+/-)-vasicine
Sergey V Shevyakov1, Olga I Davydova, Dmitry G Pershin
1Chemical Diversity Research Institute, Khimki, Moscow Reg., 114401 Russia.
Abstract:
A reliable and high-yielding procedure for preparation of 7-aryl and 7-heteroaryl derivatives of (+/-)-vasicine in two steps from the naturally occurring material is described. This protocol broadens the chemical space for selective modifications of the vasicine tricyclic structure, thereby making it a valuable starting point for the development of novel compound libraries with potentially beneficial biological profiles.
More Related Videos
Related Concept Videos
Diels–Alder Reaction Forming Bridged Bicyclic Products: Stereochemistry
Aromatic Compounds: Overview
In 1825, Faraday isolated benzene...
Synthesis of α-Substituted Carbonyl Compounds: The Stork Enamine Reaction
Diels–Alder Reaction Forming Cyclic Products: Stereochemistry
Structure-Activity Relationships and Drug Design
SAR studies the intricate relationship between a drug's chemical structure and biological activity. It focuses on understanding how modifications to a drug's structure can influence its...
Cholinergic Antagonists: Chemistry and Structure-Activity Relationship

