Investigation of the acid catalysed Diels-Alder reaction of furan derivatives with β-ferrocenyl-α-enones
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference19 articles.
1. The α:β ratio in the acetylation of furan and the “extended selectivity treatment” for electrophilic substitutions at the beta position of the furan ring
2. Electrophilic Substitutions of Five-Membered Rings
3. Catalytic enantioselective diels-alder addition to furan provides a direct synthetic route to many chiral natural products
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1. Cross-conjugated ferrocenyl derivative furan-2-yl-(ferrocenyl)methanone: synthesis, structural analysis, docking and antibacterial evaluation;Spectroscopy Letters;2021-05-28
2. Synthesis of ferrocene substituted dihydrofuran derivatives via manganese(III) acetate mediated radical addition-cyclization reactions;Tetrahedron;2017-12
3. Synthesis and biological activity of ferrocenyl furoyl derivatives;Inorganic and Nano-Metal Chemistry;2017-02-16
4. Redox-mediated reactions of vinylferrocene: toward redox auxiliaries;Dalton Transactions;2016
5. ChemInform Abstract: Investigation of the Acid-Catalyzed Diels-Alder Reaction of Furan Derivatives with β-Ferrocenyl-α-enones.;ChemInform;2010-06-18
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