Highly stereoselective and enantiodivergent synthesis of cyclopropylphosphonates with engineered carbene transferases
Xinkun Ren, Ajay L. Chandgude, Daniela Maria Carminati, Zhuofan Shen, Sagar D. Khare, Rudi Fasan
Abstract
gram scale) with up to 99% de and ee. Mechanistic studies provide insights into factors that contribute to make this reaction inherently more challenging than hemoprotein-catalyzed olefin cyclopropanation with ethyl diazoacetate investigated previously. This work expands the range of synthetically useful, enzyme-catalyzed transformations and paves the way to the development of metalloprotein catalysts for abiological carbene transfer reactions involving non-canonical carbene donor reagents.
Topics & Concepts
CyclopropanationCarbeneChemistryStereoselectivityCombinatorial chemistryEnantioselective synthesisDiazoOlefin fiberCarbenoidCatalysisReagentSubstrate (aquarium)StereochemistryEnantiomerEthyl diazoacetateOrganic chemistryRhodiumBiologyEcologyCyclopropane Reaction MechanismsClick Chemistry and ApplicationsFluorine in Organic Chemistry