Asymmetric aldol reaction of an isocyanoacetate with aldehydes bychiral ferrocenylphosphine-gold(I) complexes: Design and preparation of new efficient ferrocenylphosphine ligands
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference11 articles.
1. Catalytic asymmetric aldol reaction: reaction of aldehydes with isocyanoacetate catalyzed by a chiral ferrocenylphosphine-gold(I) complex
2. Asymmetric Synthesis Catalyzed by Chiral Ferrocenylphosphine–Transition Metal Complexes. I. Preparation of Chiral Ferrocenylphosphines
3. Asymmetric synthesis catalyzed by transition-metal complexes with functionalized chiral ferrocenylphosphine ligands
4. 15. Preparation ofL-threonine. Interconversion of the four stereoisomeric α-amino-β-hydroxybutyric acids
5. A stereoselective synthesis of threo-threonine reaction of isocyanoacetate with acetaldehyde.
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2. Silver‐Catalyzed Asymmetric Aldol Reaction of Isocyanoacetic Acid Derivatives Enabled by Cooperative Participation of Classical and Nonclassical Hydrogen Bonds;Advanced Synthesis & Catalysis;2022-06-21
3. Ferrocenyl Gold Complexes as Efficient Catalysts;European Journal of Inorganic Chemistry;2022-03-15
4. Catalytic Enantioselective Isocyanide‐Based Reactions: Beyond Passerini and Ugi Multicomponent Reactions;Chemistry – A European Journal;2021-03-05
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