An efficient route for the allylation of arylaldehydes to give enantiopure homoallylic alcohols
Author:
Publisher
Elsevier BV
Subject
Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Catalysis
Reference51 articles.
1. Enantioselective addition of organozinc reagents to aldehydes
2. Mild and efficient barbier allylation reaction mediated by magnesium powder under solvent-free conditions
3. Use of Cyclic Allylic Bromides in the Zinc–Mediated Aqueous Barbier–Grignard Reaction
4. The Solvent-Free Addition Reaction of Allylzinc Bromide and Carbonyl Compounds
5. Catalytic Asymmetric Cyanohydrin Synthesis
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1. Highly Enantioselective Allylation Reactions of Aldehydes with Allyltrimethylsilane Catalyzed by a Chiral Oxazaborolidinium Ion;Organic Letters;2020-06-18
2. Study on Tin Powder-Promoted Allylation of 3-Aryl-3-hydroxy-2-oxindoles;Chinese Journal of Organic Chemistry;2020
3. Organocatalyzed Synthesis of 2-Amino-4H-Chromenes: An Enantioselective Approach;Current Organocatalysis;2018-07-27
4. Tin Powder-Mediated One-Pot Protocols for Allylation Reactions by Allylic Halides;Current Organic Synthesis;2018-02-08
5. Stereoselective synthesis of vic-halohydrins and an unusual Knoevenagel product from an organocatalyzed aldol reaction: A non-enamine mode;Chinese Journal of Catalysis;2015-07
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