Head et al., 1931 - Google Patents
CLXIV.—Hydroxy-carbonyl compounds. Part I. A synthesis of scopoletinHead et al., 1931
- Document ID
- 10328317790944437751
- Author
- Head F
- Robertson A
- Publication year
- Publication venue
- Journal of the Chemical Society (Resumed)
External Links
Snippet
In order to overcome the difficulties encountered in unsuccessful attempts to prepare 2: 4- dihydroxyanisole directly from 5-nitroguaiacol it was considered necessary to protect the hydroxyl group of the nitro-compound. Moreover, it was essential that the protecting group …
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 C1=CC(=O)OC2=C1C=C(OC)C(O)=C2 0 title description 17
Classifications
-
- 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
- C07D311/04—Benzo[b]pyrans, not hydrogenated in the carbocyclic ring
- C07D311/22—Benzo[b]pyrans, not hydrogenated in the carbocyclic ring with oxygen or sulfur atoms directly attached in position 4
- C07D311/26—Benzo[b]pyrans, not hydrogenated in the carbocyclic ring with oxygen or sulfur atoms directly attached in position 4 with aromatic rings attached in position 2 or 3
- C07D311/28—Benzo[b]pyrans, not hydrogenated in the carbocyclic ring with oxygen or sulfur atoms directly attached in position 4 with aromatic rings attached in position 2 or 3 with aromatic rings attached in position 2 only
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C39/00—Compounds having at least one hydroxy or O-metal group bound to a carbon atom of a six-membered aromatic ring
- C07C39/12—Compounds having at least one hydroxy or O-metal group bound to a carbon atom of a six-membered aromatic ring polycyclic with no unsaturation outside the aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D215/00—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
- C07D215/02—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
- C07D215/16—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
- C07C69/76—Esters of carboxylic acids having a carboxyl group bound to a carbon atom of a six-membered aromatic ring
-
- 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
- C07C45/45—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by condensation
- C07C45/46—Friedel-Crafts reactions
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C65/00—Compounds having carboxyl groups bound to carbon atoms of six-membered aromatic rings and containing any of the groups OH, O-metal, -CHO, keto, ether, groups, groups, or groups
- C07C65/01—Compounds having carboxyl groups bound to carbon atoms of six-membered aromatic rings and containing any of the groups OH, O-metal, -CHO, keto, ether, groups, groups, or groups containing hydroxy or O-metal groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C205/00—Compounds containing nitro groups bound to a carbon skeleton
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C37/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom of a six-membered aromatic ring
- C07C37/01—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom of a six-membered aromatic ring by replacing functional groups bound to a six-membered aromatic ring by hydroxy groups, e.g. by hydrolysis
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C49/00—Ketones; Ketenes; Dimeric ketenes; Ketonic chelates
- C07C49/76—Ketones containing a keto group bound to a six-membered aromatic ring
- C07C49/82—Ketones containing a keto group bound to a six-membered aromatic ring containing hydroxy groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C07D209/04—Indoles; Hydrogenated indoles
- C07D209/30—Indoles; Hydrogenated indoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to carbon atoms of the hetero ring
- C07D209/32—Oxygen atoms
- C07D209/34—Oxygen atoms in position 2
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C50/00—Quinones
- C07C50/26—Quinones containing groups having oxygen atoms singly bound to carbon atoms
- C07C50/28—Quinones containing groups having oxygen atoms singly bound to carbon atoms with monocyclic quinoid structure
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Narasimhachari et al. | A note on the components of the bark of Prunus puddum | |
Robertson et al. | CCXCIII.—A synthesis of pyrylium salts of anthocyanidin type. Part XIV | |
Levy et al. | CCCLXXIV.—Experiments on the synthesis of the anthocyanins. Part VIII. A synthesis of œnin chloride | |
Balakrishna et al. | Nuclear oxidation in flavones and related compounds: Part XXV. Isomers of pedicinin | |
Borrows et al. | 237. The chemistry of the pyrrocolines. Part II. Nitroso-derivatives of some substituted pyrrocolines | |
Baker et al. | 396. The synthesis of 5-hydroxy-8-methoxyflavone (primetin monomethyl ether) | |
Rao et al. | Isolation and constitution of quercetagitrin, a glucoside of quercetagetin | |
Narasimhachari et al. | Synthetic experiments in the benzopyrone series: Part XIV. Synthesis of santal | |
Bhattacharya et al. | A Synthesis of Morindone | |
Robinson et al. | XII.—Anthoxanthins. Part VIII. A synthesis of morin and of 5: 7: 2′: 4′-tetrahydroxyflavone | |
Heidelberger et al. | CERTAIN AMINO AND ACYLAMINO PHENOL ETHERS. | |
Gnagy | SOME DIHYDROXYPHENONES AND DERIVATIVES1 | |
Briggs et al. | 175. Flavonols from the bark of Melicope ternata. Part III. A synthesis of quercetin 3: 3′-dimethyl ether, quercetin 3: 7: 3′-trimethyl ether, quercetin 3: 5: 7: 3′-tetramethyl ether, ternatin, and related benzyl ethers | |
Morgan et al. | LXVI.—Researches on residual affinity and coordination. Part III. Reactions of selenium and tellurium acetylacetones | |
Chakravarti et al. | XXVII.—Synthesis of 3: 10-dimethoxytetrahydroprotoberberine | |
Robertson et al. | 182. Lichen acids. Part II. The constitution of evernic acid and the synthesis of methyl evernate | |
Reeves et al. | The Synthesis of a New Dimethyl-β-methyl-glucoside | |
Rapson | 57. Constituents of the leaves of certain Leucadendron species. Part I. Leucodrin |