[go: up one dir, main page]
More Web Proxy on the site http://driver.im/

Fujimoto et al., 2020 - Google Patents

Anion-Accelerated Aromatic Oxy-Cope Rearrangement in Geranylation/Nerylation of Xanthone: Stereochemical Insights and Synthesis of Fuscaxanthone F

Fujimoto 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 …
Continue reading at www.thieme-connect.com (other versions)

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D213/00Heterocyclic 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
    • C07D213/02Heterocyclic 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
    • C07D213/04Heterocyclic 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
    • C07D213/06Heterocyclic 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D487/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by C07D451/00 - C07D477/00
    • C07D487/02Heterocyclic 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
    • C07D487/04Ortho-condensed systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C45/00Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D311/00Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings
    • C07D311/02Heterocyclic 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C41/00Preparation of ethers; Preparation of compounds having groups, groups or groups
    • C07C41/01Preparation of ethers
    • C07C41/18Preparation of ethers by reactions not forming ether-oxygen bonds
    • C07C41/30Preparation of ethers by reactions not forming ether-oxygen bonds by increasing the number of carbon atoms, e.g. by oligomerisation
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D307/00Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
    • C07D307/02Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07FACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F17/00Metallocenes
    • C07F17/02Metallocenes of metals of Groups 8, 9 or 10 of the Periodic System
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2103/00Systems 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