Enantioselective Diels-Alder reactions between cyclopentadiene and α,β-acetylenic aldehydes catalyzed by a chiral super Lewis acid
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference11 articles.
1. Mechanistic studies of a CAB-catalyzed asymmetric Diels-Alder reaction
2. The origin of greater than 200:1 enantioselectivity in a catalytic Diels-Alder reaction as revealed by physical and chemical studies
3. C2-Symmetric Cationic Copper(II) Complexes as Chiral Lewis Acids: Counterion Effects in the Enantioselective Diels–Alder Reaction
4. A New Powerful and Practical BLA Catalyst for Highly Enantioselective Diels−Alder Reaction: An Extreme Acceleration of Reaction Rate by Brønsted Acid
5. Demonstration of the Synthetic Power of Oxazaborolidine-Catalyzed Enantioselective Diels-Alder Reactions by Very Efficient Routes to Cassiol and Gibberellic Acid
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3. Designing aromatic heterocyclic superacids in terms of Brønsted and Lewis perspectives;Physical Chemistry Chemical Physics;2020
4. Chiral Supramolecular U-Shaped Catalysts Induce the Multiselective Diels–Alder Reaction of Propargyl Aldehyde;Journal of the American Chemical Society;2018-11-07
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