JP2005510605A5 - - Google Patents
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- JP2005510605A5 JP2005510605A5 JP2003547493A JP2003547493A JP2005510605A5 JP 2005510605 A5 JP2005510605 A5 JP 2005510605A5 JP 2003547493 A JP2003547493 A JP 2003547493A JP 2003547493 A JP2003547493 A JP 2003547493A JP 2005510605 A5 JP2005510605 A5 JP 2005510605A5
- Authority
- JP
- Japan
- Prior art keywords
- aryl
- formula
- compound
- cycloalkyl
- branched
- 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.)
- Granted
Links
- 239000000203 mixture Substances 0.000 claims description 29
- 125000003118 aryl group Chemical group 0.000 claims description 28
- 125000000217 alkyl group Chemical group 0.000 claims description 24
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 20
- 238000000034 method Methods 0.000 claims description 17
- 229910052698 phosphorus Inorganic materials 0.000 claims description 17
- 150000001875 compounds Chemical class 0.000 claims description 15
- -1 ketal Chemical group 0.000 claims description 14
- LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 claims description 14
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims description 11
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 claims description 11
- 239000011574 phosphorus Substances 0.000 claims description 11
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 10
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 10
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims description 10
- DHKHKXVYLBGOIT-UHFFFAOYSA-N acetaldehyde Diethyl Acetal Natural products CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 claims description 10
- 125000002777 acetyl group Chemical class [H]C([H])([H])C(*)=O 0.000 claims description 10
- 125000004104 aryloxy group Chemical group 0.000 claims description 10
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 10
- 229910052794 bromium Inorganic materials 0.000 claims description 10
- 239000000460 chlorine Substances 0.000 claims description 10
- 229910052801 chlorine Inorganic materials 0.000 claims description 10
- 150000004292 cyclic ethers Chemical class 0.000 claims description 10
- 125000000000 cycloalkoxy group Chemical group 0.000 claims description 10
- 150000002148 esters Chemical class 0.000 claims description 10
- 229910052731 fluorine Inorganic materials 0.000 claims description 10
- 239000011737 fluorine Substances 0.000 claims description 10
- 229910052739 hydrogen Inorganic materials 0.000 claims description 10
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 10
- 238000005801 aryl-aryl coupling reaction Methods 0.000 claims description 8
- 239000001257 hydrogen Substances 0.000 claims description 8
- 125000001624 naphthyl group Chemical group 0.000 claims description 8
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 8
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 claims description 6
- 125000004390 alkyl sulfonyl group Chemical group 0.000 claims description 6
- 125000001118 alkylidene group Chemical group 0.000 claims description 6
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 6
- 238000007334 copolymerization reaction Methods 0.000 claims description 6
- 229910052760 oxygen Inorganic materials 0.000 claims description 6
- 239000001301 oxygen Substances 0.000 claims description 6
- 125000004437 phosphorous atom Chemical group 0.000 claims description 6
- 150000003335 secondary amines Chemical class 0.000 claims description 6
- 150000003457 sulfones Chemical class 0.000 claims description 6
- 150000003462 sulfoxides Chemical class 0.000 claims description 6
- 150000003512 tertiary amines Chemical class 0.000 claims description 6
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 4
- 229910052783 alkali metal Inorganic materials 0.000 claims description 4
- 150000001340 alkali metals Chemical class 0.000 claims description 4
- 125000004183 alkoxy alkyl group Chemical group 0.000 claims description 4
- 125000003545 alkoxy group Chemical group 0.000 claims description 4
- 125000005243 carbonyl alkyl group Chemical group 0.000 claims description 4
- 150000003983 crown ethers Chemical class 0.000 claims description 4
- 125000004185 ester group Chemical group 0.000 claims description 4
- 150000002431 hydrogen Chemical class 0.000 claims description 4
- 150000002825 nitriles Chemical class 0.000 claims description 4
- 229920000642 polymer Polymers 0.000 claims description 4
- 125000006835 (C6-C20) arylene group Chemical group 0.000 claims description 2
- PPTXVXKCQZKFBN-UHFFFAOYSA-N (S)-(-)-1,1'-Bi-2-naphthol Chemical compound C1=CC=C2C(C3=C4C=CC=CC4=CC=C3O)=C(O)C=CC2=C1 PPTXVXKCQZKFBN-UHFFFAOYSA-N 0.000 claims description 2
- 238000005727 Friedel-Crafts reaction Methods 0.000 claims description 2
- 125000002947 alkylene group Chemical group 0.000 claims description 2
- 150000001412 amines Chemical class 0.000 claims description 2
- 125000005418 aryl aryl group Chemical group 0.000 claims description 2
- ZADPBFCGQRWHPN-UHFFFAOYSA-N boronic acid Chemical compound OBO ZADPBFCGQRWHPN-UHFFFAOYSA-N 0.000 claims description 2
- 125000005620 boronic acid group Chemical group 0.000 claims description 2
- 229910052799 carbon Inorganic materials 0.000 claims description 2
- 239000011203 carbon fibre reinforced carbon Substances 0.000 claims description 2
- 125000002993 cycloalkylene group Chemical group 0.000 claims description 2
- 125000005028 dihydroxyaryl group Chemical group 0.000 claims description 2
- 125000001188 haloalkyl group Chemical group 0.000 claims description 2
- 230000001590 oxidative effect Effects 0.000 claims description 2
- 238000005954 phosphonylation reaction Methods 0.000 claims description 2
- OJMIONKXNSYLSR-UHFFFAOYSA-N phosphorous acid Chemical compound OP(O)O OJMIONKXNSYLSR-UHFFFAOYSA-N 0.000 claims description 2
- 238000006116 polymerization reaction Methods 0.000 claims description 2
- 230000000379 polymerizing effect Effects 0.000 claims description 2
- 239000002243 precursor Substances 0.000 claims description 2
- 125000001424 substituent group Chemical group 0.000 claims description 2
- OBSZRRSYVTXPNB-UHFFFAOYSA-N tetraphosphorus Chemical compound P12P3P1P32 OBSZRRSYVTXPNB-UHFFFAOYSA-N 0.000 claims 2
- 238000006467 substitution reaction Methods 0.000 claims 1
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 17
- 229910052751 metal Inorganic materials 0.000 description 14
- 239000002184 metal Substances 0.000 description 14
- 239000003054 catalyst Substances 0.000 description 10
- 238000005669 hydrocyanation reaction Methods 0.000 description 8
- 150000007517 lewis acids Chemical class 0.000 description 7
- 229910052759 nickel Inorganic materials 0.000 description 7
- 150000002978 peroxides Chemical class 0.000 description 7
- 239000002841 Lewis acid Substances 0.000 description 6
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 6
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 6
- 150000002894 organic compounds Chemical class 0.000 description 6
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 5
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 5
- CFEYBLWMNFZOPB-UHFFFAOYSA-N Allylacetonitrile Natural products C=CCCC#N CFEYBLWMNFZOPB-UHFFFAOYSA-N 0.000 description 4
- 229910021591 Copper(I) chloride Inorganic materials 0.000 description 4
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 4
- RAHZWNYVWXNFOC-UHFFFAOYSA-N Sulphur dioxide Chemical compound O=S=O RAHZWNYVWXNFOC-UHFFFAOYSA-N 0.000 description 4
- OXBLHERUFWYNTN-UHFFFAOYSA-M copper(I) chloride Chemical compound [Cu]Cl OXBLHERUFWYNTN-UHFFFAOYSA-M 0.000 description 4
- 238000007037 hydroformylation reaction Methods 0.000 description 4
- FBAFATDZDUQKNH-UHFFFAOYSA-M iron chloride Chemical compound [Cl-].[Fe] FBAFATDZDUQKNH-UHFFFAOYSA-M 0.000 description 4
- 238000006317 isomerization reaction Methods 0.000 description 4
- JMANVNJQNLATNU-UHFFFAOYSA-N oxalonitrile Chemical compound N#CC#N JMANVNJQNLATNU-UHFFFAOYSA-N 0.000 description 4
- MHOVAHRLVXNVSD-UHFFFAOYSA-N rhodium atom Chemical compound [Rh] MHOVAHRLVXNVSD-UHFFFAOYSA-N 0.000 description 4
- JIAARYAFYJHUJI-UHFFFAOYSA-L zinc dichloride Chemical compound [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 0.000 description 4
- 0 CC=C(C(C(C(OP(*)*)=CC)=C(C=CC=C1)C1=I)=C(C=CC=C1)C1=C)OP(C)* Chemical compound CC=C(C(C(C(OP(*)*)=CC)=C(C=CC=C1)C1=I)=C(C=CC=C1)C1=C)OP(C)* 0.000 description 3
- 229910017052 cobalt Inorganic materials 0.000 description 3
- 239000010941 cobalt Substances 0.000 description 3
- 229910052763 palladium Inorganic materials 0.000 description 3
- 229910052703 rhodium Inorganic materials 0.000 description 3
- 239000010948 rhodium Substances 0.000 description 3
- UVKXJAUUKPDDNW-NSCUHMNNSA-N (e)-pent-3-enenitrile Chemical compound C\C=C\CC#N UVKXJAUUKPDDNW-NSCUHMNNSA-N 0.000 description 2
- WBAXCOMEMKANRN-UHFFFAOYSA-N 2-methylbut-3-enenitrile Chemical compound C=CC(C)C#N WBAXCOMEMKANRN-UHFFFAOYSA-N 0.000 description 2
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 2
- 229910007926 ZrCl Inorganic materials 0.000 description 2
- XXROGKLTLUQVRX-UHFFFAOYSA-N allyl alcohol Chemical compound OCC=C XXROGKLTLUQVRX-UHFFFAOYSA-N 0.000 description 2
- 150000002118 epoxides Chemical class 0.000 description 2
- 229910052741 iridium Inorganic materials 0.000 description 2
- GKOZUEZYRPOHIO-UHFFFAOYSA-N iridium atom Chemical compound [Ir] GKOZUEZYRPOHIO-UHFFFAOYSA-N 0.000 description 2
- 125000003253 isopropoxy group Chemical group [H]C([H])([H])C([H])(O*)C([H])([H])[H] 0.000 description 2
- 229910052697 platinum Inorganic materials 0.000 description 2
- 235000005074 zinc chloride Nutrition 0.000 description 2
- 239000011592 zinc chloride Substances 0.000 description 2
- WUCQRXWCJPCWTQ-NSCUHMNNSA-N (e)-pent-3-enal Chemical compound C\C=C\CC=O WUCQRXWCJPCWTQ-NSCUHMNNSA-N 0.000 description 1
- SDRZFSPCVYEJTP-UHFFFAOYSA-N 1-ethenylcyclohexene Chemical compound C=CC1=CCCCC1 SDRZFSPCVYEJTP-UHFFFAOYSA-N 0.000 description 1
- JIGUICYYOYEXFS-UHFFFAOYSA-N 3-tert-butylbenzene-1,2-diol Chemical compound CC(C)(C)C1=CC=CC(O)=C1O JIGUICYYOYEXFS-UHFFFAOYSA-N 0.000 description 1
- 150000001299 aldehydes Chemical class 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- WUCQRXWCJPCWTQ-UHFFFAOYSA-N trans-3-pentenal Natural products CC=CCC=O WUCQRXWCJPCWTQ-UHFFFAOYSA-N 0.000 description 1
- UIUWNILCHFBLEQ-NSCUHMNNSA-N trans-pent-3-enoic acid Chemical compound C\C=C\CC(O)=O UIUWNILCHFBLEQ-NSCUHMNNSA-N 0.000 description 1
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US09/994,097 US20030135014A1 (en) | 2001-11-26 | 2001-11-26 | Polymeric, phosphorus-containing compositions and their use in hydrocyanation, isomerization and hydroformylation reactions |
| PCT/US2002/036919 WO2003046049A1 (en) | 2001-11-26 | 2002-11-18 | Polymeric, phosphorous-containing compositions and their use in hydrocyanation, isomerization and hydroformylation reactions |
Related Child Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2008266795A Division JP4343258B2 (ja) | 2001-11-26 | 2008-10-15 | 高分子リン含有組成物、およびヒドロシアン化反応、異性化反応およびヒドロホルミル化反応におけるそれらの使用 |
| JP2008266794A Division JP4382865B2 (ja) | 2001-11-26 | 2008-10-15 | 高分子リン含有組成物、およびヒドロシアン化反応、異性化反応およびヒドロホルミル化反応におけるそれらの使用 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2005510605A JP2005510605A (ja) | 2005-04-21 |
| JP2005510605A5 true JP2005510605A5 (enExample) | 2006-01-05 |
| JP4382487B2 JP4382487B2 (ja) | 2009-12-16 |
Family
ID=25540273
Family Applications (3)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2003547493A Expired - Fee Related JP4382487B2 (ja) | 2001-11-26 | 2002-11-18 | 高分子リン含有組成物、およびヒドロシアン化反応、異性化反応およびヒドロホルミル化反応におけるそれらの使用 |
| JP2008266794A Expired - Fee Related JP4382865B2 (ja) | 2001-11-26 | 2008-10-15 | 高分子リン含有組成物、およびヒドロシアン化反応、異性化反応およびヒドロホルミル化反応におけるそれらの使用 |
| JP2008266795A Expired - Fee Related JP4343258B2 (ja) | 2001-11-26 | 2008-10-15 | 高分子リン含有組成物、およびヒドロシアン化反応、異性化反応およびヒドロホルミル化反応におけるそれらの使用 |
Family Applications After (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2008266794A Expired - Fee Related JP4382865B2 (ja) | 2001-11-26 | 2008-10-15 | 高分子リン含有組成物、およびヒドロシアン化反応、異性化反応およびヒドロホルミル化反応におけるそれらの使用 |
| JP2008266795A Expired - Fee Related JP4343258B2 (ja) | 2001-11-26 | 2008-10-15 | 高分子リン含有組成物、およびヒドロシアン化反応、異性化反応およびヒドロホルミル化反応におけるそれらの使用 |
Country Status (15)
| Country | Link |
|---|---|
| US (1) | US20030135014A1 (enExample) |
| EP (3) | EP1448668B1 (enExample) |
| JP (3) | JP4382487B2 (enExample) |
| KR (1) | KR100938961B1 (enExample) |
| CN (1) | CN1307237C (enExample) |
| AU (1) | AU2002352762A1 (enExample) |
| BR (1) | BR0215096A (enExample) |
| CA (1) | CA2468129A1 (enExample) |
| DE (3) | DE60233686D1 (enExample) |
| ES (2) | ES2271357T3 (enExample) |
| MX (1) | MXPA04004941A (enExample) |
| MY (3) | MY145761A (enExample) |
| PL (1) | PL371119A1 (enExample) |
| TW (1) | TWI245780B (enExample) |
| WO (1) | WO2003046049A1 (enExample) |
Families Citing this family (25)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2850966B1 (fr) * | 2003-02-10 | 2005-03-18 | Rhodia Polyamide Intermediates | Procede de fabrication de composes dinitriles |
| FR2854891B1 (fr) | 2003-05-12 | 2006-07-07 | Rhodia Polyamide Intermediates | Procede de preparation de dinitriles |
| EP1676632A1 (de) * | 2004-12-28 | 2006-07-05 | Covion Organic Semiconductors GmbH | Verfahren zur Herstellung von Polymeren |
| EP1948591A1 (en) * | 2005-10-18 | 2008-07-30 | INVISTA Technologies S.à.r.l. | Process of making 3-aminopentanenitrile |
| JP2009530278A (ja) | 2006-03-17 | 2009-08-27 | インビスタ テクノロジーズ エス エイ アール エル | 塩基性添加剤による処理でトリ有機ホスファイトを精製する方法 |
| US7880028B2 (en) * | 2006-07-14 | 2011-02-01 | Invista North America S.A R.L. | Process for making 3-pentenenitrile by hydrocyanation of butadiene |
| US7709674B2 (en) | 2006-07-14 | 2010-05-04 | Invista North America S.A R.L | Hydrocyanation process with reduced yield losses |
| US7919646B2 (en) * | 2006-07-14 | 2011-04-05 | Invista North America S.A R.L. | Hydrocyanation of 2-pentenenitrile |
| CN101687658B (zh) | 2007-05-14 | 2013-07-24 | 因温斯特技术公司 | 高效反应器和方法 |
| CN101952004B (zh) | 2007-06-13 | 2015-08-12 | 因温斯特技术公司 | 改善己二腈质量的方法 |
| WO2009091790A1 (en) | 2008-01-15 | 2009-07-23 | Invista Technologies S.A.R.L. | Hydrocyanation of pentenenitriles |
| EP2229354B1 (en) | 2008-01-15 | 2013-03-20 | Invista Technologies S.à.r.l. | Process for making and refining 3-pentenenitrile, and for refining 2-methyl-3-butenenitrile |
| US20090240068A1 (en) * | 2008-03-19 | 2009-09-24 | Invista North America S.A.R.L. | Methods of making cyclododecatriene and methods of making laurolactone |
| US8247621B2 (en) | 2008-10-14 | 2012-08-21 | Invista North America S.A.R.L. | Process for making 2-secondary-alkyl-4,5-di-(normal-alkyl)phenols |
| CN102471218B (zh) * | 2009-08-07 | 2014-11-05 | 因温斯特技术公司 | 用于形成二酯的氢化并酯化 |
| DK2614070T3 (en) | 2010-09-07 | 2017-10-16 | Invista Technologies Sarl | NICKEL COMPOSITIONS FOR THE MANUFACTURE OF NICKEL METAL AND NICKEL COMPLEXS |
| JP5556773B2 (ja) * | 2010-09-10 | 2014-07-23 | 信越化学工業株式会社 | ナフタレン誘導体及びその製造方法、レジスト下層膜材料、レジスト下層膜形成方法及びパターン形成方法 |
| CN104371092B (zh) * | 2013-08-12 | 2016-12-28 | 中国科学技术大学 | 一种含联二萘结构的侧链磺化聚酮及其制备方法 |
| JP6403554B2 (ja) * | 2013-12-04 | 2018-10-10 | 日本化薬株式会社 | フェノール樹脂、エポキシ樹脂、エポキシ樹脂組成物、およびその硬化物 |
| JP6605828B2 (ja) * | 2015-03-30 | 2019-11-13 | 日鉄ケミカル＆マテリアル株式会社 | 多価ヒドロキシ樹脂、エポキシ樹脂、それらの製造方法、エポキシ樹脂組成物及びその硬化物 |
| CN106397781A (zh) * | 2016-09-07 | 2017-02-15 | 辽宁石油化工大学 | 具有中心离子调节荧光发射性质的配位聚合物的制备方法 |
| CN116332728A (zh) * | 2020-02-10 | 2023-06-27 | 广东欧凯新材料有限公司 | 一种制备公斤级新型联苯四酚的氧化偶联方法及其催化剂 |
| CN111943816B (zh) * | 2020-07-23 | 2021-04-23 | 安徽海华科技集团有限公司 | 一种2,6-二叔丁基对甲酚的制备方法 |
| CN113264847B (zh) * | 2021-04-23 | 2023-04-11 | 浙江新和成股份有限公司 | 一种己二腈的制备方法 |
| CN113817157B (zh) * | 2021-09-28 | 2022-08-16 | 四川大学 | 一种半芳香族聚酰胺缩聚催化剂及其制备方法 |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| TW315370B (enExample) * | 1994-10-07 | 1997-09-11 | Du Pont | |
| JP3892931B2 (ja) * | 1997-03-11 | 2007-03-14 | 高砂香料工業株式会社 | ２個のビニル基を有する光学活性ホスフィン誘導体、それをモノマーとするポリマー、及びそれらの遷移金属錯体 |
| US6121184A (en) * | 1997-07-29 | 2000-09-19 | E. I. Du Pont De Nemours And Company | Supported bis(phosphorus) ligands |
| US6229052B1 (en) * | 1998-05-29 | 2001-05-08 | E. I. Du Pont De Nemours And Company | Hydroformylation of olefins using supported bis(phosphorus) ligands |
| FR2790477B1 (fr) * | 1999-03-01 | 2001-05-25 | Rhodia Chimie Sa | Polymere lineaire optiquement actif utilisable comme ligand dans la preparation de complexes metalliques destines a la catalyse asymetrique |
| US6420611B1 (en) * | 1999-09-20 | 2002-07-16 | E. I. Du Pont De Nemours And Company | Composition comprising polymeric phosphite |
| US6380421B1 (en) * | 1999-09-20 | 2002-04-30 | E. I. Du Pont De Nemours And Company | Multidentate phosphite ligands, catalytic compositions containing such ligands and catalytic processes utilizing such catalytic compositions |
| US6284865B1 (en) * | 1999-09-20 | 2001-09-04 | E. I. Du Pont De Nemours And Company | Polymeric phosphite composition and hydrocyanation of unsaturated organic compounds and the isomerization of unsaturated nitriles |
-
2001
- 2001-11-26 US US09/994,097 patent/US20030135014A1/en not_active Abandoned
-
2002
- 2002-08-27 TW TW091119387A patent/TWI245780B/zh not_active IP Right Cessation
- 2002-11-18 WO PCT/US2002/036919 patent/WO2003046049A1/en not_active Ceased
- 2002-11-18 CA CA002468129A patent/CA2468129A1/en not_active Abandoned
- 2002-11-18 MX MXPA04004941A patent/MXPA04004941A/es unknown
- 2002-11-18 AU AU2002352762A patent/AU2002352762A1/en not_active Abandoned
- 2002-11-18 BR BR0215096-4A patent/BR0215096A/pt not_active Application Discontinuation
- 2002-11-18 ES ES02789715T patent/ES2271357T3/es not_active Expired - Lifetime
- 2002-11-18 KR KR1020047007935A patent/KR100938961B1/ko not_active Expired - Fee Related
- 2002-11-18 PL PL02371119A patent/PL371119A1/xx not_active Application Discontinuation
- 2002-11-18 DE DE60233686T patent/DE60233686D1/de not_active Expired - Lifetime
- 2002-11-18 DE DE60213848T patent/DE60213848T2/de not_active Expired - Lifetime
- 2002-11-18 JP JP2003547493A patent/JP4382487B2/ja not_active Expired - Fee Related
- 2002-11-18 ES ES05076031T patent/ES2314554T3/es not_active Expired - Lifetime
- 2002-11-18 EP EP02789715A patent/EP1448668B1/en not_active Expired - Lifetime
- 2002-11-18 CN CNB028275152A patent/CN1307237C/zh not_active Expired - Fee Related
- 2002-11-18 EP EP05076031A patent/EP1571172B1/en not_active Expired - Lifetime
- 2002-11-18 EP EP05076346A patent/EP1586598B1/en not_active Expired - Lifetime
- 2002-11-18 DE DE60229563T patent/DE60229563D1/de not_active Expired - Lifetime
- 2002-11-26 MY MYPI20070211A patent/MY145761A/en unknown
- 2002-11-26 MY MYPI20024427A patent/MY137180A/en unknown
- 2002-11-26 MY MYPI20070210A patent/MY145806A/en unknown
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2008
- 2008-10-15 JP JP2008266794A patent/JP4382865B2/ja not_active Expired - Fee Related
- 2008-10-15 JP JP2008266795A patent/JP4343258B2/ja not_active Expired - Fee Related
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