Application of arylboron difluoride Lewis acid catalysts to the Diels-Alder reaction: Convenient, non-volatile alternatives to boron trifluoride
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference27 articles.
1. Diels-Alder-Reactions Part I: New Preparative Aspects
Cited by 9 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Leveraging Metal and Ligand Reactive Sites for One Pot Reactions: Ligand‐Centered Borenium Ions for Tandem Catalysis with Palladium;Chemistry – A European Journal;2022-09-26
2. Preparation of Organotrifluoroborate Salts: Precipitation-Driven Equilibrium under Non-Etching Conditions;Angewandte Chemie International Edition;2012-08-17
3. Preparation of Organotrifluoroborate Salts: Precipitation-Driven Equilibrium under Non-Etching Conditions;Angewandte Chemie;2012-08-17
4. Organotrifluoroborate Hydrolysis: Boronic Acid Release Mechanism and an Acid–Base Paradox in Cross-Coupling;Journal of the American Chemical Society;2012-04-19
5. ChemInform Abstract: Application of Arylboron Difluoride Lewis Acid Catalysts to the Diels-Alder Reaction: Convenient, Nonvolatile Alternatives to Boron Trifluoride.;ChemInform;2010-06-13
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