Fujimoto et al., 2020 - Google Patents
Anion-Accelerated Aromatic Oxy-Cope Rearrangement in Geranylation/Nerylation of Xanthone: Stereochemical Insights and Synthesis of Fuscaxanthone FFujimoto et al., 2020
- Document ID
- 14278457865848207887
- Author
- Fujimoto Y
- Takahashi K
- Kobayashi R
- Fukaya H
- Yanai H
- Matsumoto T
- Publication year
- Publication venue
- Synlett
External Links
Snippet
An efficient installation of a 3, 7-dimethylocta-2, 6-dien-1-yl (geranyl or neryl) side chain at the C (1) position of a xanthone core by utilizing an anion-accelerated aromatic oxy-Cope rearrangement is described. Experiments revealed that this uncommon rearrangement takes …
- 238000006550 Oxy-Cope rearrangement reaction 0 title abstract description 25
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/06—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom containing only hydrogen and carbon atoms in addition to the ring nitrogen atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D311/00—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings
- C07D311/02—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings ortho- or peri-condensed with carbocyclic rings or ring systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C41/00—Preparation of ethers; Preparation of compounds having groups, groups or groups
- C07C41/01—Preparation of ethers
- C07C41/18—Preparation of ethers by reactions not forming ether-oxygen bonds
- C07C41/30—Preparation of ethers by reactions not forming ether-oxygen bonds by increasing the number of carbon atoms, e.g. by oligomerisation
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/02—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F17/00—Metallocenes
- C07F17/02—Metallocenes of metals of Groups 8, 9 or 10 of the Periodic System
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2103/00—Systems containing at least three condensed rings
Similar Documents
Publication | Publication Date | Title |
---|---|---|
Varala et al. | Chemoselective Michael type addition of aliphatic amines to α, β-ethylenic compounds using bismuth triflate catalyst | |
Fujita et al. | Nucleophilic 5-endo-trig cyclization of 3, 3-difluoroallylic ketone enolates: synthesis of 5-fluorinated 2-alkylidene-2, 3-dihydrofurans | |
Fujimoto et al. | Anion-Accelerated Aromatic Oxy-Cope Rearrangement in Geranylation/Nerylation of Xanthone: Stereochemical Insights and Synthesis of Fuscaxanthone F | |
Huang et al. | Samarium Diiodide Catalyzed Radical Cascade Cyclizations that Construct Quaternary Stereocenters | |
Kitamura et al. | 2-Azido-1, 3-dimethylimidazolinium chloride: an efficient diazo transfer reagent for 1, 3-dicarbonyl compounds | |
Tarui et al. | Stereoselective Suzuki Coupling Reaction of an α-Bromo-α-fluoro-β-lactam | |
Tumma et al. | Synthetic studies towards stachybotrin C | |
Capitta et al. | Enantioselective organocatalyzed desymmetrization of 3-substituted cyclobutanones through Michael addition to nitroalkenes | |
Cossy et al. | Synthesis of indatraline using a Suzuki cross-coupling reaction and a chemoselective hydrogenation: A versatile approach | |
Wang et al. | Halogen cation induced stereoselective semipinacol-type rearrangement of allylic alcohols: a highly efficient approach to α-quaternary β-haloketo compounds | |
Jovanović et al. | Acid-Catalyzed [3+ 2] Cycloaddition of Enones with Azomethine Imines for Easy Access to Tetrahydropyrazolopyrazolones | |
Ballini et al. | A General Procedure for theOne-pot Preparation of Polyfunctionalized Nitrocyclopropanes | |
Fujimoto et al. | Concise Total Synthesis of Elliptoxanthone A by Utilizing Aromatic Oxy-Cope Rearrangement for Efficient C-Isoprenylation of Xanthone Skeleton | |
Du et al. | Chiral Gold Complex Catalyzed Tandem Dehydrative Cyclization/Hetero-Diels–Alder Reaction | |
Millet et al. | Copper-catalyzed kinetic resolution of 1, 3-cyclohexadiene monoepoxide with Grignard reagents | |
Peppe et al. | Indium (I) bromide-mediated regioselective markovnikov hydroselenation, diselenation and hydration of terminal alkynes with diphenyldiselenide in aqueous media | |
Someya et al. | A new approach to 4-aryl-1, 3-butanediols by cobalt-catalyzed sequential radical cyclization-arylation reaction of silicon-tethered 6-iodo-1-hexene derivatives | |
Doi et al. | RuHCl (CO)(PPh3) 3-catalyzed reductive dimerization of α, β-unsaturated aldehydes leading to α-hydroxymethyl ketones | |
D’hooghe et al. | Coupling of 1-Alkyl-2-(bromomethyl) aziridines with Lithium Dialkylcuprates towards 1, 2-Dialkylaziridines | |
Wang et al. | Total Synthesis of (+)-Mintlactone and (–)-Isomintlactone via SmI2-Induced Radical Cyclization | |
Iwasaki et al. | Synthesis of β, γ-unsaturated ketones by allylation of pentamethylcyclopentadienyl ketones followed by removal of pentamethylcyclopentadiene | |
Morton et al. | Corey-Chaykovsky reaction of chiral sulfinyl imines: A convenient procedure for the formation of chiral aziridines | |
Lefranc et al. | Direct Organocatalytic Construction of Bicyclo [3.2. 1] octanes by Domino Michael/Aldol Reaction with β, γ-Unsaturated 1, 2-Keto Amides | |
Watanabe et al. | Novel synthesis of fused indoles by the palladium-catalyzed cyclization of N-cycloalkenyl-o-haloanilines | |
Rauhut et al. | Stereoselective Preparation of Cyclopropylmagnesium Reagents via a Br-Mg Exchange Using i-PrMgCl× LiCl in the Presence of Dioxane |