CA1192186A - Process for preparing glucose penta-acetate and xyclose tetra-acetate - Google Patents
Process for preparing glucose penta-acetate and xyclose tetra-acetateInfo
- Publication number
- CA1192186A CA1192186A CA000424771A CA424771A CA1192186A CA 1192186 A CA1192186 A CA 1192186A CA 000424771 A CA000424771 A CA 000424771A CA 424771 A CA424771 A CA 424771A CA 1192186 A CA1192186 A CA 1192186A
- Authority
- CA
- Canada
- Prior art keywords
- acetate
- glucose
- xylose
- diacetate
- acetic acid
- 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
- 239000001083 [(2R,3R,4S,5R)-1,2,4,5-tetraacetyloxy-6-oxohexan-3-yl] acetate Substances 0.000 title claims abstract description 15
- UAOKXEHOENRFMP-ZJIFWQFVSA-N [(2r,3r,4s,5r)-2,3,4,5-tetraacetyloxy-6-oxohexyl] acetate Chemical compound CC(=O)OC[C@@H](OC(C)=O)[C@@H](OC(C)=O)[C@H](OC(C)=O)[C@@H](OC(C)=O)C=O UAOKXEHOENRFMP-ZJIFWQFVSA-N 0.000 title claims abstract description 14
- 238000004519 manufacturing process Methods 0.000 title abstract description 4
- MJOQJPYNENPSSS-XQHKEYJVSA-N [(3r,4s,5r,6s)-4,5,6-triacetyloxyoxan-3-yl] acetate Chemical compound CC(=O)O[C@@H]1CO[C@@H](OC(C)=O)[C@H](OC(C)=O)[C@H]1OC(C)=O MJOQJPYNENPSSS-XQHKEYJVSA-N 0.000 title 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims abstract description 102
- WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 claims abstract description 81
- SRBFZHDQGSBBOR-IOVATXLUSA-N D-xylopyranose Chemical compound O[C@@H]1COC(O)[C@H](O)[C@H]1O SRBFZHDQGSBBOR-IOVATXLUSA-N 0.000 claims abstract description 30
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 claims abstract description 23
- WQZGKKKJIJFFOK-VFUOTHLCSA-N beta-D-glucose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 claims abstract description 22
- 239000008103 glucose Substances 0.000 claims abstract description 22
- 238000006243 chemical reaction Methods 0.000 claims abstract description 18
- ZYPMNZKYVVSXOJ-YNEHKIRRSA-N [(2r,3s,4r)-2,3,4-triacetyloxy-5-oxopentyl] acetate Chemical compound CC(=O)OC[C@@H](OC(C)=O)[C@H](OC(C)=O)[C@@H](OC(C)=O)C=O ZYPMNZKYVVSXOJ-YNEHKIRRSA-N 0.000 claims abstract description 16
- PYMYPHUHKUWMLA-UHFFFAOYSA-N arabinose Natural products OCC(O)C(O)C(O)C=O PYMYPHUHKUWMLA-UHFFFAOYSA-N 0.000 claims abstract description 15
- 238000000034 method Methods 0.000 claims abstract description 15
- SRBFZHDQGSBBOR-UHFFFAOYSA-N beta-D-Pyranose-Lyxose Natural products OC1COC(O)C(O)C1O SRBFZHDQGSBBOR-UHFFFAOYSA-N 0.000 claims abstract description 14
- FUGNBFBPAQNNCV-GBQQWJQBSA-N acetic acid;(2r,3s,4r)-2,3,4,5-tetrahydroxypentanal Chemical compound CC(O)=O.CC(O)=O.OC[C@@H](O)[C@H](O)[C@@H](O)C=O FUGNBFBPAQNNCV-GBQQWJQBSA-N 0.000 claims abstract description 11
- GCRZMZYBFQQNLX-FAOVPRGRSA-N CC(O)=O.CC(O)=O.OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C=O Chemical compound CC(O)=O.CC(O)=O.OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C=O GCRZMZYBFQQNLX-FAOVPRGRSA-N 0.000 claims abstract description 10
- VMHLLURERBWHNL-UHFFFAOYSA-M Sodium acetate Chemical group [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 claims description 14
- 239000003054 catalyst Substances 0.000 claims description 10
- 229910052783 alkali metal Inorganic materials 0.000 claims description 5
- -1 alkali metal acetate Chemical class 0.000 claims description 5
- 239000001632 sodium acetate Substances 0.000 claims description 5
- 235000017281 sodium acetate Nutrition 0.000 claims description 5
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical group CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 claims description 5
- 239000003377 acid catalyst Substances 0.000 claims description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 4
- 239000011541 reaction mixture Substances 0.000 claims description 2
- CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 claims 1
- 229930006000 Sucrose Natural products 0.000 claims 1
- 239000005720 sucrose Substances 0.000 claims 1
- 235000000346 sugar Nutrition 0.000 abstract description 12
- 239000000047 product Substances 0.000 abstract description 10
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 abstract description 6
- 239000006227 byproduct Substances 0.000 abstract description 4
- 238000011282 treatment Methods 0.000 abstract description 4
- 229960000583 acetic acid Drugs 0.000 description 26
- 235000011054 acetic acid Nutrition 0.000 description 26
- 229960001031 glucose Drugs 0.000 description 18
- 235000001727 glucose Nutrition 0.000 description 17
- 229960003487 xylose Drugs 0.000 description 11
- 229940040526 anhydrous sodium acetate Drugs 0.000 description 9
- 229940022663 acetate Drugs 0.000 description 6
- 150000001242 acetic acid derivatives Chemical class 0.000 description 6
- 150000008064 anhydrides Chemical class 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 229960004249 sodium acetate Drugs 0.000 description 4
- 238000003756 stirring Methods 0.000 description 4
- 238000006640 acetylation reaction Methods 0.000 description 3
- 238000005194 fractionation Methods 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- 150000008163 sugars Chemical class 0.000 description 3
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 2
- KFSLWBXXFJQRDL-UHFFFAOYSA-N Peracetic acid Chemical compound CC(=O)OO KFSLWBXXFJQRDL-UHFFFAOYSA-N 0.000 description 2
- VJHCJDRQFCCTHL-BTVCFUMJSA-N acetic acid;(2r,3s,4r,5r)-2,3,4,5,6-pentahydroxyhexanal Chemical compound CC(O)=O.OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C=O VJHCJDRQFCCTHL-BTVCFUMJSA-N 0.000 description 2
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 description 2
- 230000021736 acetylation Effects 0.000 description 2
- KJIFKLIQANRMOU-UHFFFAOYSA-N oxidanium;4-methylbenzenesulfonate Chemical compound O.CC1=CC=C(S(O)(=O)=O)C=C1 KJIFKLIQANRMOU-UHFFFAOYSA-N 0.000 description 2
- 238000004064 recycling Methods 0.000 description 2
- 238000010992 reflux Methods 0.000 description 2
- 239000000725 suspension Substances 0.000 description 2
- 241000282326 Felis catus Species 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- VJMAITQRABEEKP-UHFFFAOYSA-N [6-(phenylmethoxymethyl)-1,4-dioxan-2-yl]methyl acetate Chemical group O1C(COC(=O)C)COCC1COCC1=CC=CC=C1 VJMAITQRABEEKP-UHFFFAOYSA-N 0.000 description 1
- 239000012345 acetylating agent Substances 0.000 description 1
- 239000012190 activator Substances 0.000 description 1
- GZCGUPFRVQAUEE-VANKVMQKSA-N aldehydo-L-glucose Chemical compound OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)C=O GZCGUPFRVQAUEE-VANKVMQKSA-N 0.000 description 1
- VTIIJXUACCWYHX-UHFFFAOYSA-L disodium;carboxylatooxy carbonate Chemical compound [Na+].[Na+].[O-]C(=O)OOC([O-])=O VTIIJXUACCWYHX-UHFFFAOYSA-L 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- CCGKOQOJPYTBIH-UHFFFAOYSA-N ethenone Chemical compound C=C=O CCGKOQOJPYTBIH-UHFFFAOYSA-N 0.000 description 1
- 229960002163 hydrogen peroxide Drugs 0.000 description 1
- 238000009776 industrial production Methods 0.000 description 1
- IPBVNPXQWQGGJP-UHFFFAOYSA-N phenyl acetate Chemical compound CC(=O)OC1=CC=CC=C1 IPBVNPXQWQGGJP-UHFFFAOYSA-N 0.000 description 1
- ZNCXUFVDFVBRDO-UHFFFAOYSA-N pyridine;sulfuric acid Chemical compound [H+].[O-]S([O-])(=O)=O.C1=CC=[NH+]C=C1 ZNCXUFVDFVBRDO-UHFFFAOYSA-N 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 229960001922 sodium perborate Drugs 0.000 description 1
- 229940045872 sodium percarbonate Drugs 0.000 description 1
- YKLJGMBLPUQQOI-UHFFFAOYSA-M sodium;oxidooxy(oxo)borane Chemical compound [Na+].[O-]OB=O YKLJGMBLPUQQOI-UHFFFAOYSA-M 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H13/00—Compounds containing saccharide radicals esterified by carbonic acid or derivatives thereof, or by organic acids, e.g. phosphonic acids
- C07H13/02—Compounds containing saccharide radicals esterified by carbonic acid or derivatives thereof, or by organic acids, e.g. phosphonic acids by carboxylic acids
- C07H13/04—Compounds containing saccharide radicals esterified by carbonic acid or derivatives thereof, or by organic acids, e.g. phosphonic acids by carboxylic acids having the esterifying carboxyl radicals attached to acyclic carbon atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Health & Medical Sciences (AREA)
- Biochemistry (AREA)
- Biotechnology (AREA)
- General Health & Medical Sciences (AREA)
- Genetics & Genomics (AREA)
- Molecular Biology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Saccharide Compounds (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB8209936 | 1982-04-02 | ||
| GB8209936 | 1982-04-02 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA1192186A true CA1192186A (en) | 1985-08-20 |
Family
ID=10529507
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA000424771A Expired CA1192186A (en) | 1982-04-02 | 1983-03-29 | Process for preparing glucose penta-acetate and xyclose tetra-acetate |
Country Status (9)
| Country | Link |
|---|---|
| US (1) | US4675393A (Sortimente) |
| EP (1) | EP0091159B1 (Sortimente) |
| JP (1) | JPS58185600A (Sortimente) |
| AU (1) | AU541026B2 (Sortimente) |
| BR (1) | BR8301659A (Sortimente) |
| CA (1) | CA1192186A (Sortimente) |
| DE (1) | DE3360762D1 (Sortimente) |
| ES (1) | ES8405419A1 (Sortimente) |
| ZA (1) | ZA832347B (Sortimente) |
Families Citing this family (47)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| ATE43612T1 (de) * | 1985-05-08 | 1989-06-15 | Akzo Nv | Verfahren zur herstellung eines esters von staerke und einer monocarbonsaeure und zusammensetzung auf basis von so hergestellter staerke. |
| DE3601098C1 (de) * | 1986-01-16 | 1987-03-26 | Maizena Gmbh | Verfahren zur Herstellung peracetylierter Zuckeralkohole mit mindestens vier C-Atomen |
| SK278834B6 (sk) * | 1992-01-17 | 1998-03-04 | Unilever Nv | Časticová bieliaca detergentná zmes |
| SK278833B6 (sk) * | 1992-01-17 | 1998-03-04 | Unilever Nv | Časticová bieliaca detergentná zmes |
| US5424420A (en) * | 1993-10-05 | 1995-06-13 | Kraft Foods, Inc. | Method for preparing saccharide polyesters by transesterification |
| US5440027A (en) * | 1993-10-05 | 1995-08-08 | Kraft General Foods, Inc. | Method for preparing saccharide fatty acid polyesters by transesterification |
| US5596085A (en) * | 1995-04-11 | 1997-01-21 | Kraft Foods, Inc. | Method for preparing polyol fatty acid polyesters by transesterification |
| DE19600159A1 (de) | 1996-01-04 | 1997-07-10 | Hoechst Ag | Bleichmittelsysteme enthaltend Bis- und Tris-(mu-oxo)-di-Mangan-Komplexsalze |
| DE19606343A1 (de) | 1996-02-21 | 1997-08-28 | Hoechst Ag | Bleichmittel |
| US5850086A (en) * | 1996-06-21 | 1998-12-15 | Regents Of The University Of Minnesota | Iron complexes for bleach activation and stereospecific oxidation |
| GB0011527D0 (en) | 2000-05-12 | 2000-06-28 | Unilever Plc | Bleach catalyst and composition and method for bleaching a substrate |
| GB0106285D0 (en) | 2001-03-14 | 2001-05-02 | Unilever Plc | Air bleaching catalysts with moderating agent |
| BR0208098A (pt) | 2001-03-14 | 2004-03-02 | Unilever Nv | Composição branqueadora |
| GB0118936D0 (en) * | 2001-08-02 | 2001-09-26 | Unilever Plc | Improvements relating to colour-safe fabric treatment compositions |
| AU2002331940B2 (en) * | 2001-09-28 | 2007-07-12 | Hydrogienic Global Technology Limited | Fluid delivery system |
| JP4708706B2 (ja) * | 2002-01-16 | 2011-06-22 | イーストマン ケミカル カンパニー | ポリマー用可塑剤としての新規炭水化物エステル及びポリオールエステル、そのような可塑剤を含む組成物及び製品並びにこれらの使用方法 |
| CA2472189A1 (en) * | 2002-02-28 | 2003-09-04 | Unilever Plc | Bleach catalyst enhancement |
| GB0205276D0 (en) * | 2002-03-06 | 2002-04-17 | Unilever Plc | Bleaching composition |
| GB0222105D0 (en) * | 2002-09-24 | 2002-10-30 | Unilever Plc | Thermally labile bleaching composition |
| EP1942117A1 (en) * | 2006-12-29 | 2008-07-09 | Sigea S.R.L. | Derivatives of acid polysaccharides |
| CN101245085B (zh) * | 2007-12-19 | 2012-02-01 | 上海同辰生物科技有限公司 | 一种三氯蔗糖的合成及纯化工艺 |
| CN101990464B (zh) | 2008-04-09 | 2013-10-23 | 巴斯夫欧洲公司 | 金属酰肼配位化合物作为氧化催化剂的用途 |
| JP5878528B2 (ja) | 2010-06-28 | 2016-03-08 | ビーエーエスエフ ソシエタス・ヨーロピアＢａｓｆ Ｓｅ | 金属を含まない漂白用組成物 |
| PL2651907T3 (pl) | 2010-12-13 | 2015-03-31 | Basf Se | Katalizatory wybielania |
| PT3011004T (pt) | 2013-06-20 | 2017-10-19 | Chemsenti Ltd | Catalisador de branqueamento e oxidação |
| WO2015022502A1 (en) | 2013-08-16 | 2015-02-19 | Chemsenti Limited | Composition |
| CN103665063B (zh) * | 2013-12-12 | 2016-04-27 | 济南尚博生物科技有限公司 | 一种制备异丙基-β-D-硫代半乳糖苷的方法 |
| WO2017076771A1 (en) | 2015-11-03 | 2017-05-11 | Basf Se | Bleach catalysts |
| EP3176157A1 (en) | 2015-12-01 | 2017-06-07 | Basf Se | Bleach catalysts |
| WO2017182295A1 (en) | 2016-04-18 | 2017-10-26 | Basf Se | Liquid cleaning compositions |
| WO2017186480A1 (en) | 2016-04-26 | 2017-11-02 | Basf Se | Metal free bleaching composition |
| EP3372663A1 (en) | 2017-03-10 | 2018-09-12 | Basf Se | Bleach catalysts |
| BR112022016985A2 (pt) | 2020-02-28 | 2022-10-25 | Catexel Tech Limited | Método de degradação |
| EP3967742A1 (en) | 2020-09-15 | 2022-03-16 | WeylChem Performance Products GmbH | Compositions comprising bleaching catalyst, manufacturing process thereof, and bleaching and cleaning agent comprising same |
| EP4008765A1 (en) | 2020-12-07 | 2022-06-08 | WeylChem Performance Products GmbH | Compositions comprising protonated triazacyclic compounds and bleaching agent and cleaning agent comprising same |
| EP4296343A1 (en) | 2022-06-24 | 2023-12-27 | WeylChem Performance Products GmbH | Compositions comprising protonated triazacyclic compounds and manganese(ii) acetate, manufacturing thereof, and bleaching and cleaning agent comprising same |
| CN120731240A (zh) | 2023-02-21 | 2025-09-30 | 巴斯夫欧洲公司 | 改性的烷氧基化聚亚烷基亚胺或改性的烷氧基化多胺 |
| WO2024175401A1 (en) | 2023-02-21 | 2024-08-29 | Basf Se | Modified alkoxylated polyalkylene imines or modified alkoxylated polyamines |
| WO2024175409A1 (en) | 2023-02-21 | 2024-08-29 | Basf Se | Modified hyperbranched alkoxylated polyalkylene imines |
| CN120882779A (zh) | 2023-03-13 | 2025-10-31 | 巴斯夫欧洲公司 | 烷氧基化含氮聚合物及其用途 |
| CN120981505A (zh) | 2023-05-05 | 2025-11-18 | 巴斯夫欧洲公司 | 可生物降解的多元醇丙氧基化物、其制备、用途以及包含它们的组合物 |
| WO2024256175A1 (en) | 2023-06-13 | 2024-12-19 | Basf Se | Stabilized cleaning compositions comprising edds and enzymes and their use |
| WO2025125117A1 (en) | 2023-12-15 | 2025-06-19 | Basf Se | Biodegradable propoxylated ethylenediamines, their preparation, uses, and compositions comprising them |
| WO2025131888A1 (en) | 2023-12-19 | 2025-06-26 | Basf Se | Modified alkoxylated polyalkylene imines or modified alkoxylated polyamines |
| WO2025180874A1 (en) | 2024-02-27 | 2025-09-04 | Basf Se | Substituted 1,3-dioxolane sulfates and their use |
| WO2025195856A1 (en) | 2024-03-19 | 2025-09-25 | Basf Se | Compositions of guerbet alkyl sulfates and their use |
| WO2025202032A1 (en) | 2024-03-26 | 2025-10-02 | Basf Se | Biodegradable alkoxylated polyols, their preparation, uses, and compositions comprising them |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2013034A (en) * | 1932-06-22 | 1935-09-03 | Niacet Chemicals Corp | Sugar acylation |
| US2174541A (en) * | 1936-03-09 | 1939-10-03 | Walthausen Victor | Solid solution of acetates of sugars |
| US2376378A (en) * | 1941-09-20 | 1945-05-22 | John D Murray | Acetylation process and product |
| US2857378A (en) * | 1956-05-15 | 1958-10-21 | Atlas Powder Co | Purification of beta-glucose pentaacetate |
| US3824286A (en) * | 1970-07-07 | 1974-07-16 | Lever Brothers Ltd | Preparation of polyacetylalkylene diamines |
| JPS5527069B2 (Sortimente) * | 1973-04-28 | 1980-07-17 |
-
1983
- 1983-03-28 DE DE8383200424T patent/DE3360762D1/de not_active Expired
- 1983-03-28 EP EP83200424A patent/EP0091159B1/en not_active Expired
- 1983-03-29 AU AU12956/83A patent/AU541026B2/en not_active Ceased
- 1983-03-29 CA CA000424771A patent/CA1192186A/en not_active Expired
- 1983-03-30 ES ES521193A patent/ES8405419A1/es not_active Expired
- 1983-03-30 BR BR8301659A patent/BR8301659A/pt not_active IP Right Cessation
- 1983-03-31 ZA ZA832347A patent/ZA832347B/xx unknown
- 1983-04-01 JP JP58057727A patent/JPS58185600A/ja active Granted
-
1985
- 1985-05-13 US US06/733,413 patent/US4675393A/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| US4675393A (en) | 1987-06-23 |
| EP0091159B1 (en) | 1985-09-11 |
| ES521193A0 (es) | 1984-06-01 |
| ZA832347B (en) | 1984-11-28 |
| DE3360762D1 (en) | 1985-10-17 |
| AU1295683A (en) | 1983-10-06 |
| JPH029035B2 (Sortimente) | 1990-02-28 |
| JPS58185600A (ja) | 1983-10-29 |
| EP0091159A1 (en) | 1983-10-12 |
| AU541026B2 (en) | 1984-12-13 |
| BR8301659A (pt) | 1983-12-13 |
| ES8405419A1 (es) | 1984-06-01 |
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