SU188508A1 - - Google Patents
Info
- Publication number
- SU188508A1 SU188508A1 SU1030129A SU1030129A SU188508A1 SU 188508 A1 SU188508 A1 SU 188508A1 SU 1030129 A SU1030129 A SU 1030129A SU 1030129 A SU1030129 A SU 1030129A SU 188508 A1 SU188508 A1 SU 188508A1
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- alanine
- optically active
- aminoanabazine
- hydrazone
- anabazine
- Prior art date
Links
- QNAYBMKLOCPYGJ-UWTATZPHSA-N D-alanine Chemical compound C[C@@H](N)C(O)=O QNAYBMKLOCPYGJ-UWTATZPHSA-N 0.000 description 5
- QNAYBMKLOCPYGJ-UHFFFAOYSA-N D-alpha-Ala Natural products CC([NH3+])C([O-])=O QNAYBMKLOCPYGJ-UHFFFAOYSA-N 0.000 description 5
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- 150000007857 hydrazones Chemical class 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- XXRCUYVCPSWGCC-UHFFFAOYSA-N Ethyl pyruvate Chemical compound CCOC(=O)C(C)=O XXRCUYVCPSWGCC-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- QNAYBMKLOCPYGJ-REOHCLBHSA-N L-alanine Chemical compound C[C@H](N)C(O)=O QNAYBMKLOCPYGJ-REOHCLBHSA-N 0.000 description 2
- 235000004279 alanine Nutrition 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 230000003287 optical effect Effects 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- JIAARYAFYJHUJI-UHFFFAOYSA-L zinc dichloride Chemical compound [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 0.000 description 2
- MTXSIJUGVMTTMU-JTQLQIEISA-N (S)-anabasine Chemical compound N1CCCC[C@H]1C1=CC=CN=C1 MTXSIJUGVMTTMU-JTQLQIEISA-N 0.000 description 1
- 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 description 1
- 241000935968 Alania Species 0.000 description 1
- -1 acyl hydrazones Chemical class 0.000 description 1
- 230000001476 alcoholic effect Effects 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 239000000706 filtrate Substances 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 239000003456 ion exchange resin Substances 0.000 description 1
- 229920003303 ion-exchange polymer Polymers 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 229920001467 poly(styrenesulfonates) Polymers 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011592 zinc chloride Substances 0.000 description 1
- 235000005074 zinc chloride Nutrition 0.000 description 1
Publications (2)
| Publication Number | Publication Date |
|---|---|
| SU188508A1 true SU188508A1 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | |
| SU188507A1 SU188507A1 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) |
Family
ID=
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| Vega et al. | The preparation of L-and D-α-amino-β-methylaminopropionic acids and the identification of the compound isolated from Cycas circinalis as the L-isomer | |
| Waisvisz et al. | The structure of the sulfur-containing moiety of bottromycin | |
| US3901942A (en) | Tetracycline derivatives substituted in the 7 position and process for preparing the same | |
| US3813317A (en) | Resolution of racemates of ring-substituted phenylalanines | |
| US3733352A (en) | Preparation of d-threo-1-p-methyl-sulfonylphenyl-2-dichloro-acet-amidopropane-1,3-diol | |
| US4436910A (en) | Process for the production of aqueous solutions of sodium salts of α-a | |
| SU188508A1 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | ||
| EP0213785A1 (en) | Method for optical resolution of DL-cysteine and (R,S)-1-(1-naphthyl)ethylamine | |
| Kanazawa et al. | Isolation and identification of γ-L-glutamylglycine from bovine brain | |
| Sheehan et al. | The synthesis of cis-and trans-3-hydroxy-L-proline, two new amino acids from the antibiotic telomycin | |
| De Haas et al. | Synthesis of mixed‐acid phosphatidylserine containing unsaturated fatty acids | |
| US4562152A (en) | Process for obtaining pure L-leucine | |
| US2833821A (en) | Preparation of calcium lysinate | |
| US3741948A (en) | Process for the preparation of n-protected - alpha - l-glutamyl - s -benzyl-l-cysteinylglysines | |
| Noll et al. | Kinetic studies on the alkali-catalyzed hydrolysis and epimerization of model alkyl and hydroxyalkyl di and tripeptides | |
| US4108723A (en) | Method for optical resolution of DL-lysine compounds | |
| US4562153A (en) | Process for the separation of L-leucine and L-isoleucine | |
| Wolfrom et al. | Amino Derivatives of Starches. Derivatives of 3, 6-Diamino-3, 6-dideoxy-D-altrose1, 2 | |
| Effenberger et al. | Amino acids; 13: Investigations on the synthesis of dl-serine from α-haloacrylic acid derivatives | |
| Seto et al. | Isolation and Structure of Urochloralic Acid from Urine of Calves Fed Trichloroethylene1 | |
| Beatty et al. | The Synthesis of D-, L-and DL-2-amino-2-carboxyethyl 2-Guanidinoethyl Hydrogen Phosphate (Lombricine) and the Identity of the Natural Compound with the D Isomer | |
| US3692781A (en) | Recovery of pure cephalexin from acidic reaction mixtures | |
| KAZUNO et al. | Stero-bile Acids and Bile Alcohols LXXV. Studies on Bile of Rana nigromaculata | |
| Gillett et al. | The Synthesis of L-glycero-Tetrulose 1-Phosphate (L-Erythrulose 1-Phosphate) | |
| US4061650A (en) | 5-Trihalogenomethyl-4,5-dihyro-oxazole-4-carboxylic acid esters |