CS274863B2 - Method of d-ribose preparation - Google Patents
Method of d-ribose preparationInfo
- Publication number
- CS274863B2 CS274863B2 CS1030587A CS1030587A CS274863B2 CS 274863 B2 CS274863 B2 CS 274863B2 CS 1030587 A CS1030587 A CS 1030587A CS 1030587 A CS1030587 A CS 1030587A CS 274863 B2 CS274863 B2 CS 274863B2
- Authority
- CS
- Czechoslovakia
- Prior art keywords
- ribose
- preparation
- arabinose
- ion exchange
- exchange resin
- Prior art date
Links
- PYMYPHUHKUWMLA-LMVFSUKVSA-N aldehydo-D-ribose Chemical compound OC[C@@H](O)[C@@H](O)[C@@H](O)C=O PYMYPHUHKUWMLA-LMVFSUKVSA-N 0.000 title abstract 9
- SRBFZHDQGSBBOR-UHFFFAOYSA-N beta-D-Pyranose-Lyxose Natural products OC1COC(O)C(O)C1O SRBFZHDQGSBBOR-UHFFFAOYSA-N 0.000 abstract 8
- PYMYPHUHKUWMLA-UHFFFAOYSA-N arabinose Natural products OCC(O)C(O)C(O)C=O PYMYPHUHKUWMLA-UHFFFAOYSA-N 0.000 abstract 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 3
- NWUYHJFMYQTDRP-UHFFFAOYSA-N 1,2-bis(ethenyl)benzene;1-ethenyl-2-ethylbenzene;styrene Chemical compound C=CC1=CC=CC=C1.CCC1=CC=CC=C1C=C.C=CC1=CC=CC=C1C=C NWUYHJFMYQTDRP-UHFFFAOYSA-N 0.000 abstract 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract 2
- SRBFZHDQGSBBOR-OWMBCFKOSA-N L-ribopyranose Chemical compound O[C@H]1COC(O)[C@@H](O)[C@H]1O SRBFZHDQGSBBOR-OWMBCFKOSA-N 0.000 abstract 2
- 239000003456 ion exchange resin Substances 0.000 abstract 2
- 229920003303 ion-exchange polymer Polymers 0.000 abstract 2
- YGKTUPPJEIOGMZ-QHPFDFDXSA-N (3r,4s,5r)-2-anilino-5-(hydroxymethyl)oxolane-3,4-diol Chemical compound O[C@@H]1[C@H](O)[C@@H](CO)OC1NC1=CC=CC=C1 YGKTUPPJEIOGMZ-QHPFDFDXSA-N 0.000 abstract 1
- SRBFZHDQGSBBOR-IOVATXLUSA-N D-xylopyranose Chemical compound O[C@@H]1COC(O)[C@H](O)[C@H]1O SRBFZHDQGSBBOR-IOVATXLUSA-N 0.000 abstract 1
- SRBFZHDQGSBBOR-STGXQOJASA-N alpha-D-lyxopyranose Chemical compound O[C@@H]1CO[C@H](O)[C@@H](O)[C@H]1O SRBFZHDQGSBBOR-STGXQOJASA-N 0.000 abstract 1
- 150000004982 aromatic amines Chemical class 0.000 abstract 1
- YOUGRGFIHBUKRS-UHFFFAOYSA-N benzyl(trimethyl)azanium Chemical group C[N+](C)(C)CC1=CC=CC=C1 YOUGRGFIHBUKRS-UHFFFAOYSA-N 0.000 abstract 1
- 230000007062 hydrolysis Effects 0.000 abstract 1
- 238000006460 hydrolysis reaction Methods 0.000 abstract 1
- 229910052751 metal Inorganic materials 0.000 abstract 1
- 239000002184 metal Substances 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- 229910052750 molybdenum Inorganic materials 0.000 abstract 1
- 239000011733 molybdenum Substances 0.000 abstract 1
- -1 molybdenum ions Chemical class 0.000 abstract 1
- 239000012452 mother liquor Substances 0.000 abstract 1
- 239000011541 reaction mixture Substances 0.000 abstract 1
- 235000000346 sugar Nutrition 0.000 abstract 1
- 150000008163 sugars Chemical class 0.000 abstract 1
- 125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 abstract 1
Landscapes
- Saccharide Compounds (AREA)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CS1030587A CS274863B2 (en) | 1987-12-31 | 1987-12-31 | Method of d-ribose preparation |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CS1030587A CS274863B2 (en) | 1987-12-31 | 1987-12-31 | Method of d-ribose preparation |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CS1030587A2 CS1030587A2 (en) | 1991-11-12 |
| CS274863B2 true CS274863B2 (en) | 1991-11-12 |
Family
ID=5448594
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CS1030587A CS274863B2 (en) | 1987-12-31 | 1987-12-31 | Method of d-ribose preparation |
Country Status (1)
| Country | Link |
|---|---|
| CS (1) | CS274863B2 (cs) |
-
1987
- 1987-12-31 CS CS1030587A patent/CS274863B2/cs unknown
Also Published As
| Publication number | Publication date |
|---|---|
| CS1030587A2 (en) | 1991-11-12 |
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