Diastereoselective Functionalization of Chiral N‐Acyl‐1,3‐oxazolidines and Their Applications in the Synthesis of Bioactive Molecules
Author:
Affiliation:
1. Laboratory of Organic Chemistry BUAP (Science Institute) 72570, Ciudad Universitaria Puebla México
Publisher
Wiley
Subject
Organic Chemistry,Physical and Theoretical Chemistry
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/ejoc.202200267
Reference88 articles.
1. The Oxazolidines.
2. Chiral non-racemic bicyclic lactams. Vehicles for the construction of natural and unnatural products containing quaternary carbon centers.
3. The Use of N ‐Boc‐1,3‐Oxazolidines as Chiral Auxiliaries in Asymmetric Synthesis
4. Control of stereochemistry in free radical reactions with oxazolidine auxiliaries
5. Origins of stereoselectivity in radical additions: reactions of alkenes and radicals bearing oxazolidine and thiazolidine amide groups
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1. Corey-Chaykovsky Reaction and Related Processes;Reference Module in Chemistry, Molecular Sciences and Chemical Engineering;2024
2. Evans’ Chiral Auxiliary‐Based Asymmetric Synthetic Methodology and Its Modern Extensions;European Journal of Organic Chemistry;2023-12-13
3. Organocatalytic Asymmetric [3 + 2]-Annulations of γ-Sulfonamido/γ-Hydroxy-α,β-Unsaturated Ketones with Cyclic N-Sulfimines: Synthesis of Chiral Polyheterotricyclic Imidazolidines and Oxazolidines;The Journal of Organic Chemistry;2022-12-29
4. Synthesis of Chiral 1,4,2-Oxazaphosphorinanes Bearing Pyridyl Substituents;Russian Journal of General Chemistry;2022-12
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