SU192809A1 - - Google Patents
Info
- Publication number
- SU192809A1 SU192809A1 SU1060367A SU1060367A SU192809A1 SU 192809 A1 SU192809 A1 SU 192809A1 SU 1060367 A SU1060367 A SU 1060367A SU 1060367 A SU1060367 A SU 1060367A SU 192809 A1 SU192809 A1 SU 192809A1
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- mol
- temperature
- ethylene sulfide
- esters
- acids
- Prior art date
Links
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 9
- VOVUARRWDCVURC-UHFFFAOYSA-N thiirane Chemical compound C1CS1 VOVUARRWDCVURC-UHFFFAOYSA-N 0.000 description 6
- 239000002253 acid Substances 0.000 description 4
- 150000007513 acids Chemical class 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 150000002148 esters Chemical class 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- -1 arsine thiocyanates Chemical class 0.000 description 2
- SELUFQBSYXBQEB-UHFFFAOYSA-N 10H-phenoxarsinine Chemical compound C1=CC=C2OC3=CC=CC=C3[AsH]C2=C1 SELUFQBSYXBQEB-UHFFFAOYSA-N 0.000 description 1
- 239000013543 active substance Substances 0.000 description 1
- RQNWIZPPADIBDY-UHFFFAOYSA-N arsenic atom Chemical class [As] RQNWIZPPADIBDY-UHFFFAOYSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- XLJMAIOERFSOGZ-UHFFFAOYSA-M cyanate Chemical compound [O-]C#N XLJMAIOERFSOGZ-UHFFFAOYSA-M 0.000 description 1
- 239000000417 fungicide Substances 0.000 description 1
- 239000000543 intermediate Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 1
- 229910052753 mercury Inorganic materials 0.000 description 1
- MYWUZJCMWCOHBA-VIFPVBQESA-N methamphetamine Chemical compound CN[C@@H](C)CC1=CC=CC=C1 MYWUZJCMWCOHBA-VIFPVBQESA-N 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SU192809A1 true SU192809A1 (enExample) |
Family
ID=
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JPS63253048A (ja) | ９，１０−エンドエタノー９，１０−ジヒドロアントラセン−１１，１１−ジカルボン酸のモノエステルまたはジエステルの合成方法 | |
| Shiraishi et al. | The structure-activity relationships in coronatine analogs and amino compounds derived from (+)-coronafacic acid | |
| SU192809A1 (enExample) | ||
| US4943679A (en) | Process for the N-ω-trifluoroacetylation of saturated aliphatic monocarboxylic α,ω-diamino acids | |
| KR19990014781A (ko) | 2-시아노-3,3-디아릴 아크릴산 에스테르의 제조방법 | |
| IE912919A1 (en) | Acylaminomethylphosphinic acids, and a process for the¹preparation of acylaminomethylphosphonic acids and¹acylaminomethylphosphinic acids | |
| SU245783A1 (ru) | Способ получения 1-алкил-2-арил(алкил)-меркапто- метил-з-карбэтокси-5-окси индолов | |
| SU187014A1 (ru) | Способ получения эфиров феноксибицикло- | |
| SU785305A1 (ru) | Способ получени транс-1-арил (алкил) сульфонил-2-диалкиламиноэтенов | |
| ES3033407T3 (en) | Method for the preparation of alkyl-4-oxo-tetrahydrofuran-2-carboxylate | |
| SU1512481A3 (ru) | Способ получени тиотетроновой кислоты | |
| SU191531A1 (enExample) | ||
| SU213880A1 (ru) | Способ получения непредельных 3-алкил-5-пропил-д4- | |
| SU302337A1 (ru) | Способ получения 3-(фенил-\,\-диалкилсульфамидо)-1-ацетоксибутана | |
| SU222372A1 (ru) | Способ получения эфиров n-карбэтоксиметилкарба- | |
| SU237147A1 (enExample) | ||
| SU203681A1 (ru) | СПОШЁ ПОЛУЧЕНИЯ Ф1ЕНИЛГИД1>&АЗИДОВдиАЛкиЛФОСФОРИстых кислот | |
| SU173233A1 (ru) | Способ получения средних фосфатов 1 ечзлиотека | |
| SU250905A1 (enExample) | ||
| SU1564992A1 (ru) | Способ получени 1-амино-2Н-5,6-диоксо-1,2,3-триазина | |
| SU323398A1 (ru) | Способ получения диэфиров пероксидикарбоновыхкислот | |
| SU256766A1 (ru) | Способ получения 1-алкокси- или 1-арилокси- | |
| SU239314A1 (ru) | Способ получения n- | |
| SU306622A1 (ru) | Лжлиотека i | |
| SU340653A1 (ru) | СПОСОБ ПОЛУЧЕНИЯ ХЛОРАНГИДРИДОВ р-АЛКОКСИАКРИЛОВЫХ КИСЛОТ |