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Recent advances in asymmetric synthesis <i>via</i> cyclopropanol intermediates

Marharyta V. Laktsevich‐Iskryk, Alaksiej L. Hurski, Maksim Ošeka, Dzmitry G. Kananovich

2024Organic & Biomolecular Chemistry19 citationsDOIOpen Access PDF

Abstract

ring-opening or with retention of the cyclopropane ring. This review summarizes stereoselective and stereoretentive transformations suitable for asymmetric synthesis. The utility of cyclopropanols is discussed for two main strategies: (i) substrate-controlled transformations using enantiomerically enriched cyclopropanol intermediates through a traditional approach, and (ii) the use of nonchiral or racemic cyclopropanols, where asymmetric induction is achieved through a chiral catalyst, representing a direction that has recently emerged.

Topics & Concepts

ChemistryComputer scienceBiochemical engineeringEngineeringCyclopropane Reaction MechanismsAsymmetric Synthesis and CatalysisAsymmetric Hydrogenation and Catalysis