Highly Diastereoselective anti-Aldol Reactions of Glycolate Titanium Enolates
Author:
Affiliation:
1. Institut für Organische Chemie, Universität des Saarlandes, 66123 Saarbrücken, Germany
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo8025466
Reference60 articles.
1. The ester enolate Claisen rearrangement. Stereochemical control through stereoselective enolate formation
2. Acyclic stereoselection. 5. Use of double stereodifferentiation to enhance 1,2 diastereoselection in aldol condensations of chiral aldehydes
3. Chiral enolate design
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1. Stereoselective Aldol Additions of Glycolic Acid and Its Derivatives;Synthesis;2019-03-25
2. Synthesis of trans -Configured Enol Ethers by a Sequence of syn -Selective Glycolate Aldol Addition, Hydrolysis, and Grob Fragmentation;European Journal of Organic Chemistry;2017-10-11
3. Titanium Enolate Chemistry at the Beginning of the 21st Century;European Journal of Organic Chemistry;2016-02-24
4. Palladium-Catalyzed Allylic Alkylation Reactions of Glycolates as a Tool for the Synthesis of Functionalized α-Hydroxy Esters;European Journal of Organic Chemistry;2015-08-03
5. Stereoselective TiCl4-Mediated Aldol Reactions Starting from Acylsilanes;European Journal of Organic Chemistry;2014-12-16
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