Controlled couplings of quinone monoacetals using reusable polystyrene-anchored specific proton catalyst
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference79 articles.
1. Reviews on preparation and synthetic utility of quinone acetals:
2. Cyclohexadienone Ketals and Quinols: Four Building Blocks Potentially Useful for Enantioselective Synthesis
3. Masked o-Benzoquinones in Organic Synthesis
4. For selected examples, see:
5. Chemistry of 4,4-dimethoxycyclohexa-2,5-dienone. Unusual formation of bridged polycyclic compounds
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1. [3 + 2] Coupling of Quinone Monoacetals with Vinyl Ethers Effected by Tetrabutylammonium Triflate: Regiocontrolled Synthesis of 2-Oxygenated Dihydrobenzofurans;Organic Letters;2021-11-08
2. Controlled-Coupling of Quinone Monoacetals by New Activation Methods: Regioselective Synthesis of Phenol-Derived Compounds;Synlett;2019-03-25
3. A catalytic asymmetric one-pot [3+2] cyclization/semipinacol rearrangement sequence: an efficient construction of a multi-substituted 3H-spiro[benzofuran-2,1′-cyclopentane] skeleton;Chemical Communications;2019
4. OxidativeCCBond Formation (Couplings, Cyclizations, Cyclopropanation, etc.);PATAI'S Chemistry of Functional Groups;2018-12-10
5. Regioselective Synthesis of Bicyclic and Polycyclic Systems by Cycloaddition Reactions of Alkenyl p-Benzoquinones;The Journal of Organic Chemistry;2017-12-08
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