Isothiourea‐Catalyzed Enantioselective Functionalisation of Glycine Schiff Base Aryl Esters via 1,6‐ and 1,4‐Additions
Abstract The enantioselective α‐functionalisation of glycine Schiff base aryl esters through isothiourea catalysis is successfully demonstrated for 1,6‐additions to para‐quinone methides (21 examples, up to 95 : 5 dr and 96 : 4 er) and 1,4‐ additions to methylene substituted dicarbonyl or disulfonyl...
Main Authors: | Lotte Stockhammer, Rebecca Craik, Prof. Dr. Uwe Monkowius, Dr. David B. Cordes, Prof. Dr. Andrew D. Smith, Prof. Dr. Mario Waser |
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Format: | Article |
Language: | English |
Published: |
Wiley-VCH
2023-07-01
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Series: | ChemistryEurope |
Subjects: | |
Online Access: | https://doi.org/10.1002/ceur.202300015 |
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