Related Experiment Video
Updated: Feb 11, 2026

Author Spotlight: Optimizing CFPS Systems for Synthetic Cell Construction
Published on: April 19, 2024
Heterocycles through Domino Reactions with Trimethyl Aconitate, a Versatile Synthetic Building Block
Daniel Witthaut1, Roland Fröhlich1, Hans J Schäfer1
1Organisch-chemisches Institut der Universität Corrensstrasse 40, 48149 Münster, Germany, Fax: (+49) 251-83-36523.
Abstract:
The multitalented synthetic reagent trimethyl aconitate (1) is a renewable raw material with a high density of functional groups that up to now has only been scarcely used as a C6 building block. Domino reactions with 1 consisting of imine additions and intramolecular acylations provide simple access to heteropolycycles in one-pot reactions. For example, 1 reacts with N-methylbenzylidenamine (2) to give the spiro[pyrrolidinone-3,3'-dihydropyrrolinone] 3 in 40 % yield.
More Related Videos
Related Concept Videos
Basicity of Heterocyclic Aromatic Amines
Nomenclature of Aryl and Heterocyclic Amines
Reaction Rate
The mathematical representation of the change in the concentration of reactants and products, over time, is the rate...
Synthetic Biology
Golden rice
Golden rice is a genetically modified...
Five-Membered Heterocyclic Aromatic Compounds: Overview
Movement Joints in Buildings
The simplest type of movement joints, working joints, are...

