Asymmetric and diastereoselective Mannich reactions using hydantoin as a chiral auxiliary
Author:
Publisher
Elsevier BV
Subject
Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Catalysis
Reference15 articles.
1. A factor affecting enantioselective reaction of a ternary complex of lithium ester enolate with imine
2. Asymmetric Synthesis of β-Substituted α-Methyl-β-amino Esters by Mannich Reaction of (S,S)-(+)-Pseudoephedrine Acetamide Derived Enolate with Imines
3. Stereocontrolled Mannich Reaction with Enolizable Imines Using (S,S)-(+)-Pseudoephedrine as Chiral Auxiliary. Asymmetric Synthesis of α,β-Disubstituted β-Aminoesters and β-Lactams
4. Addition of titanium ester enolates to aldimines containing a chiral α-methylbenzylamine moiety: synthesis of chiral syn-β-amino esters
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1. Enantioselective synthesis of hydantoins by chiral acid-catalysed condensation of glyoxals and ureas;Chemical Science;2023
2. Phase-Transfer-Catalyzed Alkylation of Hydantoins;ACS Organic & Inorganic Au;2022-02-09
3. Synthesis of Chiral Hydantoins and Thiazolidinediones via Iridium‐Catalyzed Asymmetric Hydrogenation;Chinese Journal of Chemistry;2022-01-23
4. Synthesis of N-aryl β-amino acid derivatives via Cu(ii)-catalyzed asymmetric 1,4-reduction in air;RSC Advances;2019
5. Stereoselective Coupling of N-tert-Butanesulfinyl Aldimines and β-Keto Acids: Access to β-Amino Ketones;The Journal of Organic Chemistry;2017-07-11
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