GB773495A - New cophosphorylation products and method of producing same - Google Patents
New cophosphorylation products and method of producing sameInfo
- Publication number
- GB773495A GB773495A GB2733553A GB2733553A GB773495A GB 773495 A GB773495 A GB 773495A GB 2733553 A GB2733553 A GB 2733553A GB 2733553 A GB2733553 A GB 2733553A GB 773495 A GB773495 A GB 773495A
- Authority
- GB
- United Kingdom
- Prior art keywords
- lactone
- fructose
- pyrogallol
- glucono
- delta
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G79/00—Macromolecular compounds obtained by reactions forming a linkage containing atoms other than silicon, sulfur, nitrogen, oxygen, and carbon with or without the latter elements in the main chain of the macromolecule
- C08G79/02—Macromolecular compounds obtained by reactions forming a linkage containing atoms other than silicon, sulfur, nitrogen, oxygen, and carbon with or without the latter elements in the main chain of the macromolecule a linkage containing phosphorus
- C08G79/04—Phosphorus linked to oxygen or to oxygen and carbon
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Saccharide Compounds (AREA)
Abstract
The invention comprises reaction products of a phosphoryl compound with (a) an aromatic compound having at least two phenolic hydroxy groups and a polyhydric alcohol or a cycloaliphatic aldehyde, or (b) an aromatic compound having at least three phenolic hydroxy groups or a phenolic glycoside derived therefrom and an oxyheterocycloaliphatic aldehyde or alcohol. Specified dihydric phenols are catechol, 3- and 4-methyl-catechol, resorcinol, orcinol, 2,6-dimethyl hydroquinone, resacetophenone and 1,8- and 1,5-dihydroxyanthraquinone. As examples of trihydric or higher phenols are mentioned pyrogallol, gallic acid, phloracetophenone, hesperetin, quercetin and morin and the glycoside hesperidin. The alcohol is preferably a sugar or a derivative, e.g. glucose, fructose, galactose, maltose, sucrose, raffinose, glucono-delta-lactone, glucuronic acid lactone, glucosamine, methylated and acetylated glucose, sorbitol and inositol. The specified aldehyde is furfural. Reaction is preferably effected between phosphoryl chloride and the other components under anhydrous conditions in the presence of a hydrogen halide sequestering agent, e.g. pyridine and other amines or bases. The products, the structure of which is uncertain, have physiological applications. In the examples, phosphoryl chloride is reacted with: (1) hesperetin and fructose; (2) pyrogallol and glucose or fructose; (3) 1,5- and 1,8-dihydroxyanthraquinone and fructose; (4) morin and fructose; (5) pyrogallol and glucono-delta-lactone; (6) gallic acid and glucono - delta - lactone; (7) pyrogallol and sucrose; (8) quercetin and glucuronic acid lactone; (9) hesperidin and glucono-delta-lactone; (10) phloroglucinol and galactose; (11) phloracetophenone and glucuronic acid lactone; (12) pyrogallol and furfural. Specification 700,761, [Group IV (b)], is referred to. Reference has been directed by the Comptroller to Specification 706,410.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB2733553A GB773495A (en) | 1953-10-05 | 1953-10-05 | New cophosphorylation products and method of producing same |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB2733553A GB773495A (en) | 1953-10-05 | 1953-10-05 | New cophosphorylation products and method of producing same |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB773495A true GB773495A (en) | 1957-04-24 |
Family
ID=10257895
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB2733553A Expired GB773495A (en) | 1953-10-05 | 1953-10-05 | New cophosphorylation products and method of producing same |
Country Status (1)
| Country | Link |
|---|---|
| GB (1) | GB773495A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US11312922B2 (en) | 2019-04-12 | 2022-04-26 | Ecolab Usa Inc. | Antimicrobial multi-purpose cleaner comprising a sulfonic acid-containing surfactant and methods of making and using the same |
-
1953
- 1953-10-05 GB GB2733553A patent/GB773495A/en not_active Expired
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US11312922B2 (en) | 2019-04-12 | 2022-04-26 | Ecolab Usa Inc. | Antimicrobial multi-purpose cleaner comprising a sulfonic acid-containing surfactant and methods of making and using the same |
| US11891586B2 (en) | 2019-04-12 | 2024-02-06 | Ecolab Usa Inc. | Highly acidic antimicrobial multi-purpose cleaner and methods of making and using the same |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| Ponder et al. | Thermal synthesis and pyrolysis of a xylan | |
| US9181293B2 (en) | Method for the synthesis of aspalathin and analogues thereof | |
| Saito et al. | Saponins from the Leaves of Aralia elata SEEM.: Araliaceae | |
| Lázár et al. | Synthesis of the non-reducing end trisaccharide of the antithrombin-binding domain of heparin and its bioisosteric sulfonic acid analogues | |
| Herczeg et al. | Synthesis and anticoagulant activity of bioisosteric sulfonic‐acid analogues of the antithrombin‐binding pentasaccharide domain of heparin | |
| Jennemann et al. | Glycoinositolphosphosphingolipids (basidiolipids) of higher mushrooms | |
| Rosen et al. | Structural analysis of glycosyl-phosphatidylinositol antigens of Leishmania major | |
| Komarova et al. | Synthesis of a biotinylated penta-α-(1→ 6)-d-glucoside based on the rational design of an α-stereoselective glucosyl donor | |
| Herczeg et al. | New synthesis of idraparinux, the non-glycosaminoglycan analogue of the antithrombin-binding domain of heparin | |
| Ono et al. | Four new iridoid glucosides from Ajuga reptans | |
| Herczeg et al. | Novel syntheses of Idraparinux, the anticoagulant pentasaccharide with indirect selective factor Xa inhibitory activity | |
| GB773495A (en) | New cophosphorylation products and method of producing same | |
| Baer et al. | Synthesis of O-β-L-fucopyranosyl-(1→ 3)-O-β-D-galactopyranosyl-(1→ 4)-D-glucopyranose (3′-O-β-L-fucopyranosyllactose) | |
| Lindberg et al. | Structural studies of the capsular polysaccharide of Klebsiella type 33 | |
| Yamada et al. | Constituents of Holothuroidea, 13. Structure of neuritogenic active ganglioside molecular species from the sea cucumber Stichopus chloronotus | |
| Tsvetkov et al. | 8-O-Sialylation of derivatives of neuraminic acid 1, 7-lactone unusual stereoselectivity | |
| Demeter et al. | Short synthesis of Idraparinux by applying a 2‐O‐methyl‐4, 6‐O‐arylmethylene thioidoside as a 1, 2‐trans‐α‐selective glycosyl donor | |
| Pearson et al. | Towards the synthesis of aryl glucuronides as potential heparanase probes. An interesting outcome in the glycosidation of glucuronic acid with 4-hydroxycinnamic acid | |
| Inagaki et al. | Biologically active glycosides from asteroidea, 43. Isolation and structure of a new neuritogenic-active ganglioside molecular species from the starfish Linckia laevigata | |
| Salamone et al. | From d-glucuronic acid to l-iduronic acid derivatives via a radical tandem decarboxylation–cyclization | |
| Brade et al. | Identification of 2‐keto‐3‐deoxy‐1, 7‐dicarboxyheptonic acid as a constituent of the lipopolysaccharide of Acinetobacter calcoaceticus NCTC 10305 | |
| Whistler et al. | 5-thio-d-glucoyranose 1-phosphate and 6-phosphate | |
| Angibeaud et al. | Stereoselective reaction of methyl α-and β-D-glycopyranosides with acetic anhydride in the presence of trimethylsilyl trifluoromethanesulphonate | |
| Dutton et al. | Comparative NMR study of rhamnobioses—applications | |
| Cardona et al. | Syntheses of the. beta.-D-glucosides of 4-and 5-hydroxy-1-naphthyl N-methylcarbamate |