PL99516B1 - Sposob wytwarzania podstawionych pochodnych organocyny - Google Patents
Sposob wytwarzania podstawionych pochodnych organocyny Download PDFInfo
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- PL99516B1 PL99516B1 PL1975198721A PL19872175A PL99516B1 PL 99516 B1 PL99516 B1 PL 99516B1 PL 1975198721 A PL1975198721 A PL 1975198721A PL 19872175 A PL19872175 A PL 19872175A PL 99516 B1 PL99516 B1 PL 99516B1
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- formula
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- ethyltrimethyl
- carbon atoms
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- KHAVLLBUVKBTBG-UHFFFAOYSA-N dec-9-enoic acid Chemical compound OC(=O)CCCCCCCC=C KHAVLLBUVKBTBG-UHFFFAOYSA-N 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- XUDOZULIAWNMIU-UHFFFAOYSA-N delta-hexenoic acid Chemical compound OC(=O)CCCC=C XUDOZULIAWNMIU-UHFFFAOYSA-N 0.000 description 1
- 230000007682 dermal toxicity Effects 0.000 description 1
- MHDVGSVTJDSBDK-UHFFFAOYSA-N dibenzyl ether Chemical compound C=1C=CC=CC=1COCC1=CC=CC=C1 MHDVGSVTJDSBDK-UHFFFAOYSA-N 0.000 description 1
- 235000005911 diet Nutrition 0.000 description 1
- 230000037213 diet Effects 0.000 description 1
- USIUVYZYUHIAEV-UHFFFAOYSA-N diphenyl ether Chemical compound C=1C=CC=CC=1OC1=CC=CC=C1 USIUVYZYUHIAEV-UHFFFAOYSA-N 0.000 description 1
- 201000010099 disease Diseases 0.000 description 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 230000001804 emulsifying effect Effects 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- NKSJNEHGWDZZQF-UHFFFAOYSA-N ethenyl(trimethoxy)silane Chemical compound CO[Si](OC)(OC)C=C NKSJNEHGWDZZQF-UHFFFAOYSA-N 0.000 description 1
- CYHFPQIAMFXACF-UHFFFAOYSA-N ethenylsulfonylmethylbenzene Chemical compound C=CS(=O)(=O)CC1=CC=CC=C1 CYHFPQIAMFXACF-UHFFFAOYSA-N 0.000 description 1
- 239000004210 ether based solvent Substances 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 229940052303 ethers for general anesthesia Drugs 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 125000000816 ethylene group Chemical group [H]C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 235000013312 flour Nutrition 0.000 description 1
- 235000011389 fruit/vegetable juice Nutrition 0.000 description 1
- 239000000417 fungicide Substances 0.000 description 1
- 238000007429 general method Methods 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 125000001188 haloalkyl group Chemical group 0.000 description 1
- RWNJOXUVHRXHSD-UHFFFAOYSA-N hept-6-enoic acid Chemical compound OC(=O)CCCCC=C RWNJOXUVHRXHSD-UHFFFAOYSA-N 0.000 description 1
- 230000003301 hydrolyzing effect Effects 0.000 description 1
- 125000004356 hydroxy functional group Chemical group O* 0.000 description 1
- 239000005457 ice water Substances 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 239000012442 inert solvent Substances 0.000 description 1
- 208000015181 infectious disease Diseases 0.000 description 1
- 238000003780 insertion Methods 0.000 description 1
- 230000037431 insertion Effects 0.000 description 1
- INQOMBQAUSQDDS-UHFFFAOYSA-N iodomethane Chemical compound IC INQOMBQAUSQDDS-UHFFFAOYSA-N 0.000 description 1
- 108010047623 iridine Proteins 0.000 description 1
- 238000002955 isolation Methods 0.000 description 1
- 239000003350 kerosene Substances 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 230000002147 killing effect Effects 0.000 description 1
- 230000001418 larval effect Effects 0.000 description 1
- 239000008263 liquid aerosol Substances 0.000 description 1
- 239000007791 liquid phase Substances 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- 239000002075 main ingredient Substances 0.000 description 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
- 239000010445 mica Substances 0.000 description 1
- 229910052618 mica group Inorganic materials 0.000 description 1
- 244000005700 microbiome Species 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- SNVLYCMNQBXYDI-UHFFFAOYSA-N n,2-dimethylundec-10-enamide Chemical compound CNC(=O)C(C)CCCCCCCC=C SNVLYCMNQBXYDI-UHFFFAOYSA-N 0.000 description 1
- CIHLCLZEHCHBDM-UHFFFAOYSA-N n-dodecylundec-10-enamide Chemical compound CCCCCCCCCCCCNC(=O)CCCCCCCCC=C CIHLCLZEHCHBDM-UHFFFAOYSA-N 0.000 description 1
- PQWQPTWZGWEGOQ-UHFFFAOYSA-N n-ethyl-2-methylbut-3-enamide Chemical compound CCNC(=O)C(C)C=C PQWQPTWZGWEGOQ-UHFFFAOYSA-N 0.000 description 1
- WKDIUZJIWOPQSX-UHFFFAOYSA-N n-ethylhex-5-enamide;n-propan-2-ylhept-6-enamide Chemical compound CCNC(=O)CCCC=C.CC(C)NC(=O)CCCCC=C WKDIUZJIWOPQSX-UHFFFAOYSA-N 0.000 description 1
- LRSCEVQEEBMAHN-UHFFFAOYSA-N n-methylbut-3-enamide Chemical compound CNC(=O)CC=C LRSCEVQEEBMAHN-UHFFFAOYSA-N 0.000 description 1
- 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- JFSKUFMRGRLRDM-UHFFFAOYSA-N n-tert-butylnon-8-enamide Chemical compound CC(C)(C)NC(=O)CCCCCCC=C JFSKUFMRGRLRDM-UHFFFAOYSA-N 0.000 description 1
- XFHJDMUEHUHAJW-UHFFFAOYSA-N n-tert-butylprop-2-enamide Chemical compound CC(C)(C)NC(=O)C=C XFHJDMUEHUHAJW-UHFFFAOYSA-N 0.000 description 1
- 210000003739 neck Anatomy 0.000 description 1
- 229910017464 nitrogen compound Inorganic materials 0.000 description 1
- 125000005187 nonenyl group Chemical group C(=CCCCCCCC)* 0.000 description 1
- CWMPPVPFLSZGCY-UHFFFAOYSA-N oct-2-enoic acid Chemical compound CCCCCC=CC(O)=O CWMPPVPFLSZGCY-UHFFFAOYSA-N 0.000 description 1
- 231100000418 oral toxicity Toxicity 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- MZDYAVCNKNXCIS-UHFFFAOYSA-N pent-2-enamide Chemical compound CCC=CC(N)=O MZDYAVCNKNXCIS-UHFFFAOYSA-N 0.000 description 1
- HVAMZGADVCBITI-UHFFFAOYSA-N pent-4-enoic acid Chemical compound OC(=O)CCC=C HVAMZGADVCBITI-UHFFFAOYSA-N 0.000 description 1
- PTLBXNLRIHABNM-UHFFFAOYSA-N pent-4-enyl(triphenoxy)silane Chemical compound C=1C=CC=CC=1O[Si](OC=1C=CC=CC=1)(CCCC=C)OC1=CC=CC=C1 PTLBXNLRIHABNM-UHFFFAOYSA-N 0.000 description 1
- RMAUSWGFDYWZDN-UHFFFAOYSA-N pent-4-enylsulfonylmethylbenzene Chemical compound C=CCCCS(=O)(=O)CC1=CC=CC=C1 RMAUSWGFDYWZDN-UHFFFAOYSA-N 0.000 description 1
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 1
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000002985 plastic film Substances 0.000 description 1
- 229920006255 plastic film Polymers 0.000 description 1
- 231100000614 poison Toxicity 0.000 description 1
- 230000007096 poisonous effect Effects 0.000 description 1
- 238000005498 polishing Methods 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- FBCQUCJYYPMKRO-UHFFFAOYSA-N prop-2-enyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCC=C FBCQUCJYYPMKRO-UHFFFAOYSA-N 0.000 description 1
- VPJDULFXCAQHRC-UHFFFAOYSA-N prop-2-enylurea Chemical compound NC(=O)NCC=C VPJDULFXCAQHRC-UHFFFAOYSA-N 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 238000010926 purge Methods 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 230000010076 replication Effects 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 229910000077 silane Inorganic materials 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 229920002379 silicone rubber Polymers 0.000 description 1
- 239000004945 silicone rubber Substances 0.000 description 1
- 231100000438 skin toxicity Toxicity 0.000 description 1
- 235000002639 sodium chloride Nutrition 0.000 description 1
- 239000004550 soluble concentrate Substances 0.000 description 1
- 238000010183 spectrum analysis Methods 0.000 description 1
- 238000010561 standard procedure Methods 0.000 description 1
- 239000008261 styrofoam Substances 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 125000003107 substituted aryl group Chemical group 0.000 description 1
- 235000000346 sugar Nutrition 0.000 description 1
- 125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 description 1
- 125000001273 sulfonato group Chemical group [O-]S(*)(=O)=O 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 230000009885 systemic effect Effects 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 235000012222 talc Nutrition 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- RWRDLPDLKQPQOW-UHFFFAOYSA-N tetrahydropyrrole Substances C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 description 1
- CZDYPVPMEAXLPK-UHFFFAOYSA-N tetramethylsilane Chemical compound C[Si](C)(C)C CZDYPVPMEAXLPK-UHFFFAOYSA-N 0.000 description 1
- 238000005979 thermal decomposition reaction Methods 0.000 description 1
- 150000003568 thioethers Chemical class 0.000 description 1
- 150000003585 thioureas Chemical class 0.000 description 1
- HPGGPRDJHPYFRM-UHFFFAOYSA-J tin(iv) chloride Chemical compound Cl[Sn](Cl)(Cl)Cl HPGGPRDJHPYFRM-UHFFFAOYSA-J 0.000 description 1
- 125000003944 tolyl group Chemical group 0.000 description 1
- RFZAULIZNBRXEM-UHFFFAOYSA-N tricyclohexyloxy(oct-7-enyl)silane Chemical compound C1CCCCC1O[Si](OC1CCCCC1)(CCCCCCC=C)OC1CCCCC1 RFZAULIZNBRXEM-UHFFFAOYSA-N 0.000 description 1
- KQPIFPBKXYBDGV-UHFFFAOYSA-M triethylstannanylium;bromide Chemical compound CC[Sn](Br)(CC)CC KQPIFPBKXYBDGV-UHFFFAOYSA-M 0.000 description 1
- GPRLSGONYQIRFK-MNYXATJNSA-N triton Chemical compound [3H+] GPRLSGONYQIRFK-MNYXATJNSA-N 0.000 description 1
- LMWYHLXLBPELFF-UHFFFAOYSA-N undec-10-enoxymethylbenzene Chemical compound C=CCCCCCCCCCOCC1=CC=CC=C1 LMWYHLXLBPELFF-UHFFFAOYSA-N 0.000 description 1
- 150000003672 ureas Chemical class 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 229960000834 vinyl ether Drugs 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 239000011345 viscous material Substances 0.000 description 1
- 230000000007 visual effect Effects 0.000 description 1
- 239000011782 vitamin Substances 0.000 description 1
- 235000013343 vitamin Nutrition 0.000 description 1
- 229940088594 vitamin Drugs 0.000 description 1
- 229930003231 vitamin Natural products 0.000 description 1
- 239000004563 wettable powder Substances 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
- 210000002268 wool Anatomy 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/22—Tin compounds
- C07F7/2224—Compounds having one or more tin-oxygen linkages
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/22—Tin compounds
- C07F7/2208—Compounds having tin linked only to carbon, hydrogen and/or halogen
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Plural Heterocyclic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US53667874A | 1974-12-26 | 1974-12-26 | |
| US53667974A | 1974-12-26 | 1974-12-26 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| PL99516B1 true PL99516B1 (pl) | 1978-07-31 |
Family
ID=27065218
Family Applications (3)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PL1975198721A PL99516B1 (pl) | 1974-12-26 | 1975-12-24 | Sposob wytwarzania podstawionych pochodnych organocyny |
| PL1975198722A PL99518B1 (pl) | 1974-12-26 | 1975-12-24 | Sposob wytwarzania czteropodstawionych organicznych zwiazkow cyny |
| PL1975186046A PL99515B1 (pl) | 1974-12-26 | 1975-12-24 | Srodek szkodnikobojczy,zwlaszcza do zwalczania owadow,barw moskitow lub chwastow |
Family Applications After (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PL1975198722A PL99518B1 (pl) | 1974-12-26 | 1975-12-24 | Sposob wytwarzania czteropodstawionych organicznych zwiazkow cyny |
| PL1975186046A PL99515B1 (pl) | 1974-12-26 | 1975-12-24 | Srodek szkodnikobojczy,zwlaszcza do zwalczania owadow,barw moskitow lub chwastow |
Country Status (18)
| Country | Link |
|---|---|
| JP (1) | JPS51125220A (xx) |
| AU (1) | AU507615B2 (xx) |
| BG (6) | BG25229A3 (xx) |
| BR (1) | BR7508582A (xx) |
| CH (1) | CH613364A5 (xx) |
| DD (2) | DD125544A5 (xx) |
| DE (2) | DE2554790A1 (xx) |
| DK (1) | DK588675A (xx) |
| EG (1) | EG12249A (xx) |
| ES (4) | ES443820A1 (xx) |
| FR (1) | FR2355850A1 (xx) |
| GB (2) | GB1542281A (xx) |
| IL (1) | IL48716A (xx) |
| LU (1) | LU74105A1 (xx) |
| NL (1) | NL7514734A (xx) |
| PL (3) | PL99516B1 (xx) |
| SE (1) | SE7514546L (xx) |
| SU (1) | SU594884A3 (xx) |
Families Citing this family (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1598451A (en) * | 1977-01-17 | 1981-09-23 | Netherlands Central Org Scient | Antifungal and/or antibacterial organotin compounds there preparation and uses |
| US4178382A (en) * | 1978-06-19 | 1979-12-11 | Uniroyal, Inc. | N-substituted triorganostannylhydro-carbylcarboxylic acid hydrazides |
| EP0077296B1 (de) * | 1981-10-08 | 1985-08-28 | Ciba-Geigy Ag | Organozinnverbindungen |
| US5882356A (en) * | 1992-10-21 | 1999-03-16 | Courtaulds Fibres (Holdings) Limited | Fibre treatment |
| GB9304887D0 (en) * | 1993-03-10 | 1993-04-28 | Courtaulds Plc | Fibre treatment |
| GB9410912D0 (en) * | 1994-06-01 | 1994-07-20 | Courtaulds Plc | Fibre treatment |
| DE19726340C2 (de) * | 1996-08-16 | 1999-05-06 | Schering Ag | Zinndendrimere, ihre Verwendung als Röntgenkontrastmittel und Verfahren zu ihrer Herstellung |
| US6417366B2 (en) | 1999-06-24 | 2002-07-09 | Abbott Laboratories | Preparation of quinoline-substituted carbonate and carbamate derivatives |
-
1975
- 1975-12-05 DE DE19752554790 patent/DE2554790A1/de active Pending
- 1975-12-18 NL NL7514734A patent/NL7514734A/xx not_active Application Discontinuation
- 1975-12-18 FR FR7538885A patent/FR2355850A1/fr active Granted
- 1975-12-22 DD DD190457A patent/DD125544A5/xx unknown
- 1975-12-22 DD DD75198309A patent/DD134323A5/xx unknown
- 1975-12-22 SE SE7514546A patent/SE7514546L/xx unknown
- 1975-12-23 IL IL48716A patent/IL48716A/xx unknown
- 1975-12-23 DE DE19752558163 patent/DE2558163A1/de not_active Withdrawn
- 1975-12-23 DK DK588675A patent/DK588675A/da unknown
- 1975-12-23 CH CH1671875A patent/CH613364A5/xx not_active IP Right Cessation
- 1975-12-23 BR BR7508582*A patent/BR7508582A/pt unknown
- 1975-12-23 ES ES443820A patent/ES443820A1/es not_active Expired
- 1975-12-24 AU AU87838/75A patent/AU507615B2/en not_active Expired
- 1975-12-24 PL PL1975198721A patent/PL99516B1/pl unknown
- 1975-12-24 EG EG759/75A patent/EG12249A/xx active
- 1975-12-24 PL PL1975198722A patent/PL99518B1/pl unknown
- 1975-12-24 LU LU74105A patent/LU74105A1/xx unknown
- 1975-12-24 PL PL1975186046A patent/PL99515B1/pl unknown
- 1975-12-25 JP JP50155747A patent/JPS51125220A/ja active Pending
- 1975-12-26 GB GB7549030A patent/GB1542281A/en not_active Expired
- 1975-12-26 SU SU752303951A patent/SU594884A3/ru active
- 1975-12-26 BG BG035346A patent/BG25229A3/xx unknown
- 1975-12-26 BG BG031926A patent/BG26352A3/xx unknown
- 1975-12-26 GB GB75@@3480778A patent/GB1542282A/en not_active Expired
- 1975-12-26 BG BG032848A patent/BG26397A3/xx unknown
- 1975-12-26 BG BG035349A patent/BG25097A3/xx unknown
- 1975-12-26 BG BG7535348A patent/BG26672A4/xx unknown
- 1975-12-26 BG BG035347A patent/BG25520A3/xx unknown
-
1977
- 1977-04-16 ES ES457899A patent/ES457899A1/es not_active Expired
- 1977-04-16 ES ES457898A patent/ES457898A1/es not_active Expired
- 1977-04-16 ES ES457897A patent/ES457897A1/es not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| AU507615B2 (en) | 1980-02-21 |
| CH613364A5 (en) | 1979-09-28 |
| DD125544A5 (xx) | 1977-05-04 |
| PL99515B1 (pl) | 1978-07-31 |
| NL7514734A (nl) | 1976-06-29 |
| FR2355850B1 (xx) | 1981-10-23 |
| SE7514546L (sv) | 1976-06-27 |
| AU8783875A (en) | 1977-06-30 |
| EG12249A (en) | 1978-09-30 |
| SU594884A3 (ru) | 1978-02-25 |
| BR7508582A (pt) | 1976-08-24 |
| ES457899A1 (es) | 1978-08-01 |
| IL48716A0 (en) | 1976-02-29 |
| IL48716A (en) | 1980-06-30 |
| BG26352A3 (bg) | 1979-03-15 |
| BG26397A3 (bg) | 1979-03-15 |
| DE2554790A1 (de) | 1976-07-01 |
| GB1542282A (en) | 1979-03-14 |
| ES443820A1 (es) | 1977-11-16 |
| ES457897A1 (es) | 1978-10-16 |
| BG25097A3 (en) | 1978-07-12 |
| GB1542281A (en) | 1979-03-14 |
| BG25229A3 (en) | 1978-08-10 |
| PL99518B1 (pl) | 1978-07-31 |
| FR2355850A1 (fr) | 1978-01-20 |
| BG25520A3 (en) | 1978-10-10 |
| DD134323A5 (de) | 1979-02-21 |
| DK588675A (da) | 1976-06-27 |
| BG26672A4 (xx) | 1979-05-15 |
| JPS51125220A (en) | 1976-11-01 |
| ES457898A1 (es) | 1978-11-01 |
| LU74105A1 (xx) | 1976-11-11 |
| DE2558163A1 (de) | 1976-07-08 |
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