Farmer et al., 1947 - Google Patents
298. The reaction of sulphur and sulphur compounds with olefinic substances. Part I. The reaction of sulphur with mono-olefins and with Δ 1: 5-diolefinsFarmer et al., 1947
- Document ID
- 11650168708384913037
- Author
- Farmer E
- Shipley F
- Publication year
- Publication venue
- Journal of the Chemical Society (Resumed)
External Links
Snippet
1520 Farmer and Shifiley: The Reaction of Sulphur and some redistribution appears to occur in the sulphides from hydroaromatic mono-olefins owing to the facility of occurrence of (probably secondary) dehydrogenation reactions. A1: 5-Olefins give in addition to diolefin …
- NINIDFKCEFEMDL-UHFFFAOYSA-N sulfur data:image/svg+xml;base64,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 data:image/svg+xml;base64,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 [S] 0 title abstract description 114
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C7/00—Purification; Separation; Use of additives
- C07C7/148—Purification; Separation; Use of additives by treatment giving rise to a chemical modification of at least one compound
-
- 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
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic System
- C07F9/02—Phosphorus compounds
- C07F9/06—Phosphorus compounds without P-C bonds
-
- 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
- C07C2101/16—The ring being unsaturated
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C11/00—Aliphatic unsaturated hydrocarbons
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C323/00—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C23/00—Compounds containing at least one halogen atom bound to a ring other than a six-membered aromatic ring
- C07C23/18—Polycyclic halogenated hydrocarbons
- C07C23/20—Polycyclic halogenated hydrocarbons with condensed rings none of which is aromatic
- C07C23/38—Polycyclic halogenated hydrocarbons with condensed rings none of which is aromatic with three condensed rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C317/00—Sulfones; Sulfoxides
- C07C317/02—Sulfones; Sulfoxides having sulfone or sulfoxide groups bound to acyclic carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C303/00—Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C5/00—Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms
- C07C5/02—Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms by hydrogenation
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C321/00—Thiols, sulfides, hydropolysulfides or polysulfides
Similar Documents
Publication | Publication Date | Title |
---|---|---|
Farmer et al. | 298. The reaction of sulphur and sulphur compounds with olefinic substances. Part I. The reaction of sulphur with mono-olefins and with Δ 1: 5-diolefins | |
Bordwell et al. | Elimination Reactions. VII. A Comparison of Some Eliminations in Open-chain and Cyclic Systems | |
Morvillo et al. | Reactions of organic halides and cyanides with bis (tricyclohexylphosphine) nickel (0) | |
Farmer et al. | Modern views on the chemistry of vulcanization changes. I. Nature of the reaction between sulfur and olefins | |
Cristol et al. | Homoallylic free radicals. A study of the rearrangement of 3, 5-cyclocholestanyl radical to cholesteryl radical | |
Bolland et al. | 111. The primary thermal oxidation product of squalene | |
Wardell et al. | Reactions of aromatic sulphenyl compounds with organotin compounds | |
Oswald et al. | Organic sulfur compounds. VII. Some addition and co-oxidation reactions of thiols with 2, 5-dimethyl-2, 4-hexadiene | |
Paquette et al. | . alpha.-Halo sulfones. VII. The Ramberg-Baecklund rearrangement of. alpha.,. alpha.-dichloromethyl sulfones | |
Williamson | The thermal decomposition of methyl linoleate hydroperoxide | |
Cunneen | 35. The addition of thio-compounds to olefins. Part II. Reactions of thiolacetic and mono-, di-, and tri-chlorothiolacetic acids | |
Hawthorne | Preparation of Trialkylboranes or Primary Alcohols from Pyridine Borane and Terminal Olefins | |
Wolfe Jr et al. | The Chemistry of Sulfur Curing. III. Effects of Zinc Oxide on the Mechanism of the Reaction of Cyclohexene with Sulfur | |
US3567608A (en) | Mercaptan synthesis using ultraviolet radiation and a promoter containing a phosphite and azobisisobutyronitrile | |
Naylor | 299. The reaction of sulphur and sulphur compounds with olefinic substances. Part II. Mechanism of the reaction of hydrogen sulphide with mono-olefins, di-isoprenes, and rubber | |
WO2003020843A1 (en) | Composition comprising phosphonium salts and their use | |
Bloomfield | 302. The reaction of sulphur and sulphur compounds with olefinic substances. Part IV. The thermal decomposition of organic polysulphides, and its contribution to the sulphur–olefin reaction | |
Neureiter | Convenient Preparations of α-Halo Sulfones and Their Use in the Synthesis of Deuterated Olefins, the Desulfurization of Alkyl Sulfones, and the Homologization of Olefins | |
Margolies et al. | 150. The products of the interaction of hydrogen selenide and ketones | |
CRONYN et al. | SULFONES. II.* ALKENES, DIENES, α, β-UNSATURATED SULFONES, AND MONOSULFONES FROM β-DISULFONES1 | |
Bloomfield | The Reaction of Sulfur and Sulfur Compounds with Olefinic Substances. IV. The Thermal Decomposition of Organic Polysulfides, and Its Contribution to the Sulfur Olefin-Reaction | |
DOUGLASS et al. | Methanesulfenyl Chloride. III. The Reactions with Methanol and Methyl Sulfite1 | |
Lyapina | The present state of research into organosulphur compounds in petroleum | |
Glazebrook et al. | The reactions of amines and sulphur with olefins. Part III. The reaction of diethylamine and sulphur with 1: 5-diolefins | |
Barton et al. | Reaction of sulfur dichloride with o-divinylbenzene |