Michael addition/pericyclization/rearrangement – a multicomponent strategy for the synthesis of substituted resorcinols
Author:
Publisher
Royal Society of Chemistry (RSC)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2012/OB/C2OB25776A
Reference18 articles.
1. Enhanced Substituted Resorcinol Hydrophobicity Augments Tyrosinase Inhibition Potency
2. Radester, a Novel Inhibitor of the Hsp90 Protein Folding Machinery
3. Total Synthesis of the Highly Potent Anti-HIV Natural Product Daurichromenic Acid along with Its Two Chromane Derivatives, Rhododaurichromanic Acids A and B
4. Selective Protein Tyrosine Phosphatase 1B Inhibitors: Targeting the Second Phosphotyrosine Binding Site with Non-Carboxylic Acid-Containing Ligands
5. Novel Synthesis of Desymmetrized Resorcinol Derivatives: Aryl Fluoride Displacement on Deactivated Substrates
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