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The Bucherer–Bergs Multicomponent Synthesis of Hydantoins—Excellence in Simplicity
The Bucherer–Bergs Multicomponent Synthesis of Hydantoins—Excellence in Simplicity
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The Bucherer–Bergs Multicomponent Synthesis of Hydantoins—Excellence in Simplicity
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The Bucherer–Bergs Multicomponent Synthesis of Hydantoins—Excellence in Simplicity
The Bucherer–Bergs Multicomponent Synthesis of Hydantoins—Excellence in Simplicity
Journal Article

The Bucherer–Bergs Multicomponent Synthesis of Hydantoins—Excellence in Simplicity

2021
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Overview
Hydantoins and their hybrids with other molecules represent a very important group of heterocycles because they exhibit diverse biological and pharmacological activities in medicinal and agrochemical applications. They also serve as key precursors in the chemical or enzymatic synthesis of significant nonnatural α-amino acids and their conjugates with medical potential. This review provides a comprehensive treatment of the synthesis of hydantoins via the Bucherer–Bergs reaction including the Hoyer modification but limited to free carbonyl compounds or carbonyl compounds protected as acetals (ketals) and cyanohydrins used as starting reaction components. In this respect, the Bucherer–Bergs reaction provides an efficient and simple method in the synthesis of important natural products as well as for the preparation of new organic compounds applicable as potential therapeutics. The scope and limitations, as well as a comparison with some other methods for preparing hydantoins, are also discussed.