A Synthetic Equivalent of 3,5-Dimethoxyphenyl Lithium. A Facile Route to 5-Substituted Resorcinols
Author:
Publisher
Informa UK Limited
Subject
Organic Chemistry
Link
http://www.tandfonline.com/doi/pdf/10.1080/00397910008087392
Reference11 articles.
1. Research at the Interface between Chemistry and Virology: Development of a Molecular Flashlight
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3. Cyclization of 3-(arylchalcogeno)propenoyl chlorides. 2. Chalcogen and substituent control in the regiochemistry of intramolecular acylation. Preparation of benzo[b]telluropyrones
4. The pigments of “dragon's blood” resin. Part VI. 3 : 5-Dihydroxydiphenyl ether
5. Synthesis of 5-Substituted Resorcinol Derivatives via Cross-Coupling Reactions
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2. Design, synthesis and biological evaluation of a series of novel 2-benzamide-4-(6-oxy-N-methyl-1-naphthamide)-pyridine derivatives as potent fibroblast growth factor receptor (FGFR) inhibitors;European Journal of Medicinal Chemistry;2018-06
3. Solvent Choice and Kinetic Isotope Effects (KIEs) Dramatically Alter Regioselectivity in the DirectedorthoMetalation (DoM) of 1,5-Dichloro-2,4-dimethoxybenzene;Chemistry - A European Journal;2014-12-02
4. ChemInform Abstract: A Synthetic Equivalent of 3,5-Dimethoxyphenyl Lithium. A Facile Route to 5-Substituted Resorcinols.;ChemInform;2000-10-03
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