Jiang et al., 2019 - Google Patents
Nucleophilic substitution of gem-difluoroalkenes with TMSNu promoted by catalytic amounts of Cs2CO3Jiang et al., 2019
- Document ID
- 1188946406370942029
- Author
- Jiang L
- Ren B
- Li B
- Zhang G
- Peng Y
- Guan Z
- Deng Q
- Publication year
- Publication venue
- The Journal of Organic Chemistry
External Links
Snippet
The efficient and practical nucleophilic cyanation and trifluoromethylation with appropriate trimethylsilyl nucleophiles were developed. Catalytic amounts of cheap and nontoxic Cs2CO3 were used to maintain a sufficiently high concentration of nucleophilic anion (CN …
- 230000003197 catalytic 0 title abstract description 34
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
- 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
- C07D213/24—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 with substituted hydrocarbon radicals attached to ring carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B37/00—Reactions without formation or introduction of functional groups containing hetero atoms, involving either the formation of a carbon-to-carbon bond between two carbon atoms not directly linked already or the disconnection of two directly linked carbon atoms
- C07B37/04—Substitution
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B53/00—Asymmetric syntheses
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B2200/00—Indexing scheme relating to specific properties of organic compounds
-
- 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
- C07C2101/00—Systems containing only non-condensed rings
- C07C2101/12—Systems containing only non-condensed rings with a six-membered ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B61/00—Other general methods
-
- 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
- C07F5/00—Compounds containing elements of Groups 3 or 13 of the Periodic System
-
- 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
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic System
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C67/00—Preparation of carboxylic acid esters
- C07C67/30—Preparation of carboxylic acid esters by modifying the acid moiety of the ester, such modification not being an introduction of an ester group
-
- 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
Similar Documents
Publication | Publication Date | Title |
---|---|---|
Jiang et al. | Nucleophilic substitution of gem-difluoroalkenes with TMSNu promoted by catalytic amounts of Cs2CO3 | |
Ahmed et al. | Access to Divergent Fluorinated Enynes and Arenes via Palladium-Catalyzed Ring-Opening Alkynylation of gem-Difluorinated Cyclopropanes | |
Su et al. | α-amino radical-mediated diverse difunctionalization of alkenes: construction of C–C, C–N, and C–S bonds | |
Xi et al. | Application of trimethylgermanyl-substituted bisphosphine ligands with enhanced dispersion interactions to copper-catalyzed hydroboration of disubstituted alkenes | |
He et al. | Copper-catalyzed regioselective 1, 4-selenosulfonylation of 1, 3-enynes to access cyanoalkylsulfonylated allenes | |
Zeng et al. | Copper-catalyzed decarboxylative difluoromethylation | |
Ahmed et al. | Palladium-catalyzed stereoselective defluorination arylation/alkenylation/alkylation of gem-difluorinated cyclopropanes | |
Yang et al. | Synthesis of alkylated monofluoroalkenes via Fe-catalyzed defluorinative cross-coupling of donor alkenes with gem-difluoroalkenes | |
Knauber et al. | Ru/Ni dual catalytic desulfinative photoredox Csp2–Csp3 cross-coupling of alkyl sulfinate salts and aryl halides | |
Kusakabe et al. | Radical relay trichloromethylacylation of alkenes through N-heterocyclic carbene catalysis | |
Huo et al. | Catalytic, enantioselective addition of alkyl radicals to alkenes via visible-light-activated photoredox catalysis with a chiral rhodium complex | |
Zhou et al. | Mechanism of silver-mediated geminal difluorination of styrenes with a fluoroiodane reagent: insights into Lewis-acid-activation model | |
Katcher et al. | Palladium-catalyzed asymmetric synthesis of allylic fluorides | |
Bhawal et al. | Catalytic transfer functionalization through shuttle catalysis | |
Suess et al. | Mechanism of copper-catalyzed hydroalkylation of alkynes: an unexpected role of dinuclear copper complexes | |
Ye et al. | Straightforward syntheses of hypervalent iodine (III) reagents mediated by selectfluor | |
Hu et al. | Copper-mediated trifluoromethylation of α-diazo esters with TMSCF3: the important role of water as a promoter | |
Teng et al. | Asymmetric C (sp)–H addition of terminal alkynes to cyclopropenes by a chiral gadolinium catalyst | |
Mo et al. | Dinuclear iron complex-catalyzed cross-coupling of primary alkyl fluorides with aryl Grignard reagents | |
Wu et al. | Pd (II)-catalyzed asymmetric oxidative 1, 2-diamination of conjugated dienes with ureas | |
Guo et al. | Redox neutral radical-relay cobalt catalysis toward C–H fluorination and amination | |
Ma et al. | Palladium-catalyzed stereoselective hydrodefluorination of tetrasubstituted gem-difluoroalkenes | |
Wang et al. | Synthesis of fluorinated compounds by nickel-catalyzed defluorinative cross-coupling reactions | |
Gupta et al. | FLP-catalyzed monoselective C–F functionalization in polyfluorocarbons at geminal or distal sites | |
Alam et al. | Direct synthesis of secondary benzylic alcohols enabled by photoredox/Ni dual-catalyzed cross-coupling |