JP2007517850A - 不斉変換触媒を製造するための方法 - Google Patents
不斉変換触媒を製造するための方法 Download PDFInfo
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- JP2007517850A JP2007517850A JP2006548403A JP2006548403A JP2007517850A JP 2007517850 A JP2007517850 A JP 2007517850A JP 2006548403 A JP2006548403 A JP 2006548403A JP 2006548403 A JP2006548403 A JP 2006548403A JP 2007517850 A JP2007517850 A JP 2007517850A
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- 239000011630 iodine Chemical group 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- DLEDOFVPSDKWEF-UHFFFAOYSA-N lithium butane Chemical compound [Li+].CCC[CH2-] DLEDOFVPSDKWEF-UHFFFAOYSA-N 0.000 description 1
- PFCFKYSBIQBHAO-UHFFFAOYSA-N lithium;methoxybenzene Chemical compound [Li+].COC1=CC=CC=[C-]1 PFCFKYSBIQBHAO-UHFFFAOYSA-N 0.000 description 1
- YLVLCBHNULZXLQ-UHFFFAOYSA-M magnesium;2h-naphthalen-2-ide;bromide Chemical compound [Mg+2].[Br-].C1=[C-]C=CC2=CC=CC=C21 YLVLCBHNULZXLQ-UHFFFAOYSA-M 0.000 description 1
- NXPHGHWWQRMDIA-UHFFFAOYSA-M magnesium;carbanide;bromide Chemical compound [CH3-].[Mg+2].[Br-] NXPHGHWWQRMDIA-UHFFFAOYSA-M 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- CSJDCSCTVDEHRN-UHFFFAOYSA-N methane;molecular oxygen Chemical compound C.O=O CSJDCSCTVDEHRN-UHFFFAOYSA-N 0.000 description 1
- DVSDBMFJEQPWNO-UHFFFAOYSA-N methyllithium Chemical compound C[Li] DVSDBMFJEQPWNO-UHFFFAOYSA-N 0.000 description 1
- 239000012452 mother liquor Substances 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- XRBCRPZXSCBRTK-UHFFFAOYSA-N phosphonous acid Chemical compound OPO XRBCRPZXSCBRTK-UHFFFAOYSA-N 0.000 description 1
- 125000004437 phosphorous atom Chemical group 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 239000002243 precursor Substances 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- LVTJOONKWUXEFR-FZRMHRINSA-N protoneodioscin Natural products O(C[C@@H](CC[C@]1(O)[C@H](C)[C@@H]2[C@]3(C)[C@H]([C@H]4[C@@H]([C@]5(C)C(=CC4)C[C@@H](O[C@@H]4[C@H](O[C@H]6[C@@H](O)[C@@H](O)[C@@H](O)[C@H](C)O6)[C@@H](O)[C@H](O[C@H]6[C@@H](O)[C@@H](O)[C@@H](O)[C@H](C)O6)[C@H](CO)O4)CC5)CC3)C[C@@H]2O1)C)[C@H]1[C@H](O)[C@H](O)[C@H](O)[C@@H](CO)O1 LVTJOONKWUXEFR-FZRMHRINSA-N 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 241000894007 species Species 0.000 description 1
- KZNICNPSHKQLFF-UHFFFAOYSA-N succinimide Chemical class O=C1CCC(=O)N1 KZNICNPSHKQLFF-UHFFFAOYSA-N 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
- NMJASRUOIRRDSX-UHFFFAOYSA-N tert-butyl(dichloro)phosphane Chemical compound CC(C)(C)P(Cl)Cl NMJASRUOIRRDSX-UHFFFAOYSA-N 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- 150000003732 xanthenes Chemical class 0.000 description 1
Classifications
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- B01J31/18—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes containing nitrogen, phosphorus, arsenic or antimony as complexing atoms, e.g. in pyridine ligands, or in resonance therewith, e.g. in isocyanide ligands C=N-R or as complexed central atoms
- B01J31/1845—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes containing nitrogen, phosphorus, arsenic or antimony as complexing atoms, e.g. in pyridine ligands, or in resonance therewith, e.g. in isocyanide ligands C=N-R or as complexed central atoms the ligands containing phosphorus
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- B01J31/1845—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes containing nitrogen, phosphorus, arsenic or antimony as complexing atoms, e.g. in pyridine ligands, or in resonance therewith, e.g. in isocyanide ligands C=N-R or as complexed central atoms the ligands containing phosphorus
- B01J31/185—Phosphites ((RO)3P), their isomeric phosphonates (R(RO)2P=O) and RO-substitution derivatives thereof
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- B01J31/18—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes containing nitrogen, phosphorus, arsenic or antimony as complexing atoms, e.g. in pyridine ligands, or in resonance therewith, e.g. in isocyanide ligands C=N-R or as complexed central atoms
- B01J31/1845—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes containing nitrogen, phosphorus, arsenic or antimony as complexing atoms, e.g. in pyridine ligands, or in resonance therewith, e.g. in isocyanide ligands C=N-R or as complexed central atoms the ligands containing phosphorus
- B01J31/1875—Phosphinites (R2P(OR), their isomeric phosphine oxides (R3P=O) and RO-substitution derivatives thereof)
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- B01J31/1895—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes containing nitrogen, phosphorus, arsenic or antimony as complexing atoms, e.g. in pyridine ligands, or in resonance therewith, e.g. in isocyanide ligands C=N-R or as complexed central atoms the ligands containing arsenic or antimony
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- B01J31/2457—Cyclic ligands, including e.g. non-condensed polycyclic ligands, the phosphine-P atom being a ring member or a substituent on the ring comprising condensed ring systems and phosphine-P atoms as substituents on a ring of the condensed system or on a further attached ring with more than one complexing phosphine-P atom comprising aliphatic or saturated rings, e.g. Xantphos
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- B01J31/2495—Ligands comprising a phosphine-P atom and one or more further complexing phosphorus atoms covered by groups B01J31/1845 - B01J31/1885, e.g. phosphine/phosphinate or phospholyl/phosphonate ligands
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- C—CHEMISTRY; METALLURGY
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- C07F17/00—Metallocenes
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- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/28—Phosphorus compounds with one or more P—C bonds
- C07F9/48—Phosphonous acids [RP(OH)2] including [RHP(=O)(OH)]; Thiophosphonous acids including [RP(SH)2], [RHP(=S)(SH)]; Derivatives thereof
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| GBGB0400720.9A GB0400720D0 (en) | 2004-01-14 | 2004-01-14 | Novel ferrocene-based phosphorus chiral phosphines |
| PCT/GB2005/000125 WO2005068478A1 (en) | 2004-01-14 | 2005-01-14 | Process for the production of asymmetric transformation catalysts |
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| JP2006548397A Pending JP2007517849A (ja) | 2004-01-14 | 2005-01-14 | メタロセン基体のキラルホスフィンまたはアルシンリガンド |
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Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2007536339A (ja) * | 2004-05-07 | 2007-12-13 | ユミコア・アクチエンゲゼルシャフト・ウント・コムパニー・コマンディットゲゼルシャフト | 均一系のエナンチオ選択的水素化触媒のためのフェロセニル配位子 |
| JP2010138116A (ja) * | 2008-12-11 | 2010-06-24 | Tosoh Corp | フェロセン誘導体およびその用途 |
Families Citing this family (19)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB0400720D0 (en) * | 2004-01-14 | 2004-02-18 | Stylacats Ltd | Novel ferrocene-based phosphorus chiral phosphines |
| US6906212B1 (en) * | 2004-06-25 | 2005-06-14 | Eastman Chemical Company | Phosphine-phosphoramidite compounds |
| US6906213B1 (en) * | 2004-06-25 | 2005-06-14 | Eastman Chemical Company | Preparation of aminophosphines |
| US20060135804A1 (en) * | 2004-12-21 | 2006-06-22 | Boaz Neil W | Tetradentate ligands and metal complexes thereof for asymmetric catalysis |
| GB0500702D0 (en) * | 2005-01-14 | 2005-02-23 | Stylacats Ltd | Novel metallocene-based phosphorus chiral phosphines |
| GB0500700D0 (en) * | 2005-01-14 | 2005-02-23 | Stylacats Ltd | Process for the manufacture of 2-alkyl-3-phenylpropionic acids and alcohols |
| CN101421285B (zh) * | 2006-04-12 | 2013-02-06 | 索尔维亚斯股份公司 | 二茂铁二膦 |
| JP5209611B2 (ja) * | 2006-05-23 | 2013-06-12 | ソルヴィーアス アクチェンゲゼルシャフト | 不斉付加反応、特に水素化における遷移金属触媒に使用されるキラルリガンド |
| JP5232989B2 (ja) * | 2006-07-18 | 2013-07-10 | 国立大学法人豊橋技術科学大学 | 光学活性2,6−ビスアミノメチルピリジン誘導体とその製造方法およびその使用 |
| BR112012016059A2 (pt) | 2009-12-29 | 2015-09-01 | Mapi Pharma Ltd | "compostos intermediários e processos para a preparação de tapentadol e compostos relacionados". |
| CN102775418B (zh) * | 2012-06-11 | 2014-12-24 | 中国人民解放军第四军医大学 | 新型手性季铵盐相转移催化剂的合成及应用 |
| CN104592313B (zh) * | 2014-12-30 | 2017-08-25 | 陕西师范大学 | 基于二茂铁的双功能氢键有机催化剂及其制备方法和应用 |
| CN104861001B (zh) * | 2015-06-11 | 2017-08-04 | 河南省科学院化学研究所有限公司 | 一种二茂铁双膦配体的制备方法 |
| US9725398B2 (en) * | 2015-07-23 | 2017-08-08 | Evonik Degussa Gmbh | Benzene-based diphosphine ligands for alkoxycarbonylation |
| ES2732998T3 (es) * | 2016-07-19 | 2019-11-27 | Evonik Operations Gmbh | Ligandos 1,1'-bis(fosfino)ferroceno para la alcoxicarbonilación |
| CN109078653A (zh) * | 2018-10-08 | 2018-12-25 | 浙江工业大学上虞研究院有限公司 | 手性二茂铁磷酸催化剂及其在不对称Friedel-Crafts反应中的应用 |
| CN112824422B (zh) * | 2019-11-21 | 2023-01-13 | 中国科学院大连化学物理研究所 | 一种手性二茂铁-吲哚双膦配体及其制备方法和其应用 |
| CN114560893B (zh) * | 2022-03-16 | 2024-02-06 | 中国科学院上海有机化学研究所 | 平面手性茂金属化合物、其合成方法及应用 |
| CN116178455B (zh) * | 2023-04-26 | 2023-08-18 | 江苏欣诺科催化剂股份有限公司 | 一种二茂铁类手性膦配体的制备方法 |
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| AU2005205224A1 (en) | 2005-07-28 |
| EP1709054A1 (en) | 2006-10-11 |
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| CA2553607A1 (en) | 2005-07-28 |
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| GB2410951B (en) | 2009-07-22 |
| GB2410951A (en) | 2005-08-17 |
| GB0400720D0 (en) | 2004-02-18 |
| US7994355B2 (en) | 2011-08-09 |
| CN1914218A (zh) | 2007-02-14 |
| EP1725570B1 (en) | 2008-08-13 |
| GB2410950B (en) | 2009-05-20 |
| AU2005205229B2 (en) | 2010-03-04 |
| US20080281106A1 (en) | 2008-11-13 |
| WO2005068477A1 (en) | 2005-07-28 |
| EP1725570A1 (en) | 2006-11-29 |
| EP1709054B1 (en) | 2009-03-04 |
| CN1914217A (zh) | 2007-02-14 |
| GB0500704D0 (en) | 2005-02-23 |
| ATE424404T1 (de) | 2009-03-15 |
| ES2313282T3 (es) | 2009-03-01 |
| ATE404573T1 (de) | 2008-08-15 |
| US20070161762A1 (en) | 2007-07-12 |
| GB0905212D0 (en) | 2009-05-13 |
| GB0500701D0 (en) | 2005-02-23 |
| JP2007517849A (ja) | 2007-07-05 |
| DE602005013062D1 (de) | 2009-04-16 |
| CA2553608A1 (en) | 2005-07-28 |
| WO2005068478A1 (en) | 2005-07-28 |
| AU2005205224B2 (en) | 2009-04-23 |
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