Combining Meyer–Schuster Rearrangement with Aldol and Mannich Reactions: Theoretical Study of the Intermediate Interception Strategy
Author:
Affiliation:
1. Department of Organic Chemistry, Arrhenius Laboratory, Stockholm University, S-106 91 Stockholm, Sweden
Publisher
American Chemical Society (ACS)
Subject
Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis
Link
https://pubs.acs.org/doi/pdf/10.1021/ja307892c
Reference21 articles.
1. Atom Economy—A Challenge for Organic Synthesis: Homogeneous Catalysis Leads the Way
2. Atom Economy: Aldol-Type Products by Vanadium-Catalyzed Additions of Propargyl Alcohols and Aldehydes
3. Vanadium-Catalyzed Addition of Propargyl Alcohols and Imines
4. The Rearrangement of ?-Acetylenic Alcohols to ?, ?-Unsaturated Carbonyl Compounds by Silylvanadate Catalysts
5. The Meyer–Schuster rearrangement for the synthesis of α,β-unsaturated carbonyl compounds
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