Related Experiment Video
Updated: Sep 26, 2026

Metabolic Glycoengineering of Sialic Acid Using N-acyl-modified Mannosamines
Published on: November 25, 2017
Cyclopentanes from N-amino-glyconolactams. A synthesis of mannostatin A
Guixian Hu1, Martin Zimmermann, Chepuri Venkata Ramana
1Laboratorium für Organische Chemie, ETH-Hönggerberg, CH-8093 Zürich, Switzerland.
Abstract:
Oxidation of a N-amino-ribonolactam with lead tetraacetate yields two cyclopentanes; the major one was transformed into the alpha-mannosidase inhibitor mannostatin A.
More Related Videos
10:17Efficient Construction of Drug-like Bispirocyclic Scaffolds Via Organocatalytic Cycloadditions of α-Imino γ-Lactones and Alkylidene Pyrazolones
Published on: February 7, 2019
08:46Regioselective O-Glycosylation of Nucleosides via the Temporary 2',3'-Diol Protection by a Boronic Ester for the Synthesis of Disaccharide Nucleosides
Published on: July 26, 2018
Related Concept Videos
Alkylation of β-Diester Enolates: Malonic Ester Synthesis
Nomenclature of Carboxylic Acid Derivatives: Amides and Nitriles
The IUPAC and common names of amides are derived from the parent carboxylic acid, by replacing the suffix “oic acid” and “ic acid,” respectively, with “amide.” In the following example, the IUPAC name ethanamide is derived from ethanoic acid, and the common name, acetamide, is obtained from acetic acid.
Loss of Carboxy Group as CO2: Decarboxylation of Malonic Acid Derivatives
Peptidoglycan Synthesis
Cyclohexenones via Michael Addition and Aldol Condensation: The Robinson Annulation
Biosynthesis of Polysaccharides