Related Experiment Video
Updated: Feb 16, 2026

Asymmetric Walkway: A Novel Behavioral Assay for Studying Asymmetric Locomotion
Published on: January 15, 2016
Asymmetric Total Synthesis of (-)-Stemonamine and Its Stereochemical Stability
Satoshi Fujita1, Keisuke Nishikawa2, Takayuki Iwata2
1Interdisciplinary Graduate School of Engineering Sciences, Kyushu University, Kasuga-koen, Kasuga, 816-8580, Japan.
Abstract:
The first asymmetric total synthesis of (-)-stemonamine is described. The key reactions included intramolecular acylation to construct the seven-membered ring and a tandem [2+2] cycloaddition-Dieckmann condensation reaction using an ynolate to form the fully substituted cyclopentenone moiety. Racemization and epimerization of the natural product were first experimentally demonstrated.
Related Concept Videos
Stereochemical Effects of Enolization
Rotation of Asymmetric Top
The relationship between the angular momentum of any rigid body and its angular velocity, both of which are vectors, involves the moment of inertia. The moment of inertia is a scalar quantity only for spherically symmetric...
Asymmetric Lipid Bilayer
Nuclear Stability
To hold positively charged protons together...
RNA Stability
mRNA Stability and Gene Expression
Cis-acting Elements involved in mRNA stability

