Related Experiment Video
Updated: Jul 11, 2026

Preparation of Enantiopure Non-Activated Aziridines and Synthesis of Biemamide B, D, and epiallo-Isomuscarine
Published on: June 13, 2022
Total synthesis of iejimalide B. An application of the Shiina macrolactonization
Dirk Schweitzer1, John J Kane, Daniel Strand
1Department of Chemistry and Biochemistry and Walther Cancer Research Center, University of Notre Dame, Notre Dame, Indiana 46556, USA.
Abstract:
The potent anticancer compound iejimalide B (1) was prepared by a total synthesis through a strategy that features Julia olefinations, Wittig olefinations, a Carreira enantioselective alkynylation, a Heck reaction, a Marshall propargylation reaction, a Stille coupling, and a Shiina macrolactonization.
Related Concept Videos
Alkylation of β-Diester Enolates: Malonic Ester Synthesis
Production of Pharmaceuticals
Alkylation of β-Ketoester Enolates: Acetoacetic Ester Synthesis
Preparation of Amides
The DCC-promoted synthesis of amides begins with the protonation of DCC by carboxylic acid. The protonation makes it a better acceptor. Next, the addition of carboxylate to the protonated carbodiimide gives a reactive acylating agent.
Subsequently, the amine acts as a nucleophile that attacks the acylating agent to form a tetrahedral intermediate. In the...
Intramolecular Claisen Condensation of Dicarboxylic Esters: Dieckmann Cyclization

