JP5223044B2 - ビス(ホスフィン)ボロニウム塩、ビス(ホスフィン)ボロニウム塩の製造方法、この製造方法により製造されるビス(ホスフィン)ボロニウム塩 - Google Patents
ビス(ホスフィン)ボロニウム塩、ビス(ホスフィン)ボロニウム塩の製造方法、この製造方法により製造されるビス(ホスフィン)ボロニウム塩 Download PDFInfo
- Publication number
- JP5223044B2 JP5223044B2 JP2007557790A JP2007557790A JP5223044B2 JP 5223044 B2 JP5223044 B2 JP 5223044B2 JP 2007557790 A JP2007557790 A JP 2007557790A JP 2007557790 A JP2007557790 A JP 2007557790A JP 5223044 B2 JP5223044 B2 JP 5223044B2
- Authority
- JP
- Japan
- Prior art keywords
- phosphine
- bis
- group
- boronium
- boronium salt
- 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.)
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- XYFCBTPGUUZFHI-UHFFFAOYSA-N Phosphine Chemical compound P XYFCBTPGUUZFHI-UHFFFAOYSA-N 0.000 title claims description 138
- 229910000073 phosphorus hydride Inorganic materials 0.000 title claims description 74
- ZKIBBIKDPHAFLN-UHFFFAOYSA-N boronium Chemical class [H][B+]([H])([H])[H] ZKIBBIKDPHAFLN-UHFFFAOYSA-N 0.000 title claims description 69
- 238000004519 manufacturing process Methods 0.000 title claims description 21
- -1 phosphine compound Chemical class 0.000 claims description 58
- VURFVHCLMJOLKN-UHFFFAOYSA-N Diphosphine Natural products PP VURFVHCLMJOLKN-UHFFFAOYSA-N 0.000 claims description 41
- 238000006243 chemical reaction Methods 0.000 claims description 28
- 125000004437 phosphorous atom Chemical group 0.000 claims description 18
- 238000003786 synthesis reaction Methods 0.000 claims description 16
- 125000000217 alkyl group Chemical group 0.000 claims description 14
- 230000015572 biosynthetic process Effects 0.000 claims description 13
- 125000001424 substituent group Chemical group 0.000 claims description 12
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 11
- 125000003118 aryl group Chemical group 0.000 claims description 10
- 229910052698 phosphorus Inorganic materials 0.000 claims description 10
- BWJRMVLPCQPWGR-UHFFFAOYSA-N boron;phosphane Chemical compound [B].P BWJRMVLPCQPWGR-UHFFFAOYSA-N 0.000 claims description 9
- 125000003545 alkoxy group Chemical group 0.000 claims description 7
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical group [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 claims description 5
- 229910018286 SbF 6 Inorganic materials 0.000 claims description 5
- 150000001450 anions Chemical class 0.000 claims description 5
- 229910052796 boron Inorganic materials 0.000 claims description 5
- 125000004122 cyclic group Chemical group 0.000 claims description 3
- 239000000126 substance Substances 0.000 claims 3
- 150000003839 salts Chemical class 0.000 claims 1
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 45
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 21
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 12
- 238000000034 method Methods 0.000 description 12
- 239000012039 electrophile Substances 0.000 description 11
- 229910052757 nitrogen Inorganic materials 0.000 description 11
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 9
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 8
- 238000005859 coupling reaction Methods 0.000 description 7
- 238000003756 stirring Methods 0.000 description 7
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 6
- 235000002597 Solanum melongena Nutrition 0.000 description 6
- 229910052717 sulfur Inorganic materials 0.000 description 6
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 4
- 238000006555 catalytic reaction Methods 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 4
- CRHWEIDCXNDTMO-UHFFFAOYSA-N ditert-butylphosphane Chemical compound CC(C)(C)PC(C)(C)C CRHWEIDCXNDTMO-UHFFFAOYSA-N 0.000 description 4
- 239000000706 filtrate Substances 0.000 description 4
- 239000013067 intermediate product Substances 0.000 description 4
- 239000010410 layer Substances 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 239000012044 organic layer Substances 0.000 description 4
- 150000003003 phosphines Chemical class 0.000 description 4
- 239000007787 solid Substances 0.000 description 4
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 4
- 229910052723 transition metal Inorganic materials 0.000 description 4
- 150000003624 transition metals Chemical class 0.000 description 4
- 125000005073 adamantyl group Chemical group C12(CC3CC(CC(C1)C3)C2)* 0.000 description 3
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 3
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 3
- GPAYUJZHTULNBE-UHFFFAOYSA-N diphenylphosphine Chemical compound C=1C=CC=CC=1PC1=CC=CC=C1 GPAYUJZHTULNBE-UHFFFAOYSA-N 0.000 description 3
- 239000003446 ligand Substances 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- 238000010898 silica gel chromatography Methods 0.000 description 3
- 238000006467 substitution reaction Methods 0.000 description 3
- 230000002194 synthesizing effect Effects 0.000 description 3
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 3
- ZDQSBZHWCMBILH-UHFFFAOYSA-N tert-butyl(methyl)phosphane Chemical compound CPC(C)(C)C ZDQSBZHWCMBILH-UHFFFAOYSA-N 0.000 description 3
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 2
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 2
- 238000011914 asymmetric synthesis Methods 0.000 description 2
- 229910000085 borane Inorganic materials 0.000 description 2
- UWTDFICHZKXYAC-UHFFFAOYSA-N boron;oxolane Chemical compound [B].C1CCOC1 UWTDFICHZKXYAC-UHFFFAOYSA-N 0.000 description 2
- AQRNIOMHNXJPFD-UHFFFAOYSA-N bromoborane methylsulfanylmethane Chemical compound BrB.CSC AQRNIOMHNXJPFD-UHFFFAOYSA-N 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 230000008878 coupling Effects 0.000 description 2
- 238000010168 coupling process Methods 0.000 description 2
- 238000004132 cross linking Methods 0.000 description 2
- 239000013078 crystal Substances 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- MCRSZLVSRGTMIH-UHFFFAOYSA-N ditert-butyl(chloro)phosphane Chemical compound CC(C)(C)P(Cl)C(C)(C)C MCRSZLVSRGTMIH-UHFFFAOYSA-N 0.000 description 2
- 229910052736 halogen Inorganic materials 0.000 description 2
- 150000002367 halogens Chemical class 0.000 description 2
- 229910052740 iodine Inorganic materials 0.000 description 2
- 239000011630 iodine Substances 0.000 description 2
- 239000012280 lithium aluminium hydride Substances 0.000 description 2
- 239000012038 nucleophile Substances 0.000 description 2
- 230000000269 nucleophilic effect Effects 0.000 description 2
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
- 230000008569 process Effects 0.000 description 2
- 125000006239 protecting group Chemical group 0.000 description 2
- 239000002994 raw material Substances 0.000 description 2
- 229910052938 sodium sulfate Inorganic materials 0.000 description 2
- 235000011152 sodium sulphate Nutrition 0.000 description 2
- 125000005951 trifluoromethanesulfonyloxy group Chemical group 0.000 description 2
- UORVGPXVDQYIDP-UHFFFAOYSA-N trihydridoboron Substances B UORVGPXVDQYIDP-UHFFFAOYSA-N 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- ANGGPYSFTXVERY-UHFFFAOYSA-N 2-iodo-2-methylpropane Chemical compound CC(C)(C)I ANGGPYSFTXVERY-UHFFFAOYSA-N 0.000 description 1
- SUXNMFSORPLKTG-UHFFFAOYSA-N CC(C)(C)PC.CC(C)(C)PC(C)(C)C.I Chemical compound CC(C)(C)PC.CC(C)(C)PC(C)(C)C.I SUXNMFSORPLKTG-UHFFFAOYSA-N 0.000 description 1
- 238000010485 C−C bond formation reaction Methods 0.000 description 1
- 238000009876 asymmetric hydrogenation reaction Methods 0.000 description 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
- UORVGPXVDQYIDP-BJUDXGSMSA-N borane Chemical group [10BH3] UORVGPXVDQYIDP-BJUDXGSMSA-N 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 229940125782 compound 2 Drugs 0.000 description 1
- 229940126214 compound 3 Drugs 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000006880 cross-coupling reaction Methods 0.000 description 1
- 239000000539 dimer Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 125000003253 isopropoxy group Chemical group [H]C([H])([H])C([H])(O*)C([H])([H])[H] 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 125000000040 m-tolyl group Chemical group [H]C1=C([H])C(*)=C([H])C(=C1[H])C([H])([H])[H] 0.000 description 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- SAWKFRBJGLMMES-UHFFFAOYSA-N methylphosphine Chemical compound PC SAWKFRBJGLMMES-UHFFFAOYSA-N 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- 125000003261 o-tolyl group Chemical group [H]C1=C([H])C(*)=C(C([H])=C1[H])C([H])([H])[H] 0.000 description 1
- AUONHKJOIZSQGR-UHFFFAOYSA-N oxophosphane Chemical compound P=O AUONHKJOIZSQGR-UHFFFAOYSA-N 0.000 description 1
- 125000001037 p-tolyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])([H])[H] 0.000 description 1
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- XOJVVFBFDXDTEG-UHFFFAOYSA-N pristane Chemical compound CC(C)CCCC(C)CCCC(C)CCCC(C)C XOJVVFBFDXDTEG-UHFFFAOYSA-N 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 238000001308 synthesis method Methods 0.000 description 1
- 238000010189 synthetic method Methods 0.000 description 1
- BDMOFMMYRRTFKS-UHFFFAOYSA-N tert-butyl(methyl)phosphanium;iodide Chemical compound [I-].C[PH2+]C(C)(C)C BDMOFMMYRRTFKS-UHFFFAOYSA-N 0.000 description 1
- 238000007832 transition metal-catalyzed coupling reaction Methods 0.000 description 1
Images
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
- 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
- C07F9/50—Organo-phosphines
- C07F9/5027—Polyphosphines
-
- 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
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/6564—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having phosphorus atoms, with or without nitrogen, oxygen, sulfur, selenium or tellurium atoms, as ring hetero atoms
- C07F9/6568—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having phosphorus atoms, with or without nitrogen, oxygen, sulfur, selenium or tellurium atoms, as ring hetero atoms having phosphorus atoms as the only ring hetero atoms
- C07F9/65688—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having phosphorus atoms, with or without nitrogen, oxygen, sulfur, selenium or tellurium atoms, as ring hetero atoms having phosphorus atoms as the only ring hetero atoms the ring phosphorus atom being part of a phosphonium compound
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Biochemistry (AREA)
- General Health & Medical Sciences (AREA)
- Molecular Biology (AREA)
Description
以下、本発明のビス(ホスフィン)ボロニウム塩を好適に合成し得る本発明のビス(ホスフィン)ボロニウム塩の製造方法(以下、本発明方法と称する)について詳細に説明する。
30mL二口ナスフラスコに水素化リチウムアルミニウム133mg及び磁気撹拌子を入れて窒素置換し、ジエチルエーテル5mLを加えて撹拌しながら0℃に冷却した。
30mL二口ナスフラスコに水素化リチウムアルミニウム229mg及び磁気撹拌子を入れて窒素置換し、ジエチルエーテル5mLを加えて撹拌しながら0℃に冷却した。
50mL二口ナスフラスコに炭酸カリウム3.04g、ヨウ化t‐ブチル(メチル)ホスホニウム1.02g及び磁気撹拌子を入れて窒素置換し、ジクロロメタン10mLを加えた。
30ml二口ナスフラスコに、ジフェニルホスフィンの10重量%ヘキサン溶液20ml及び磁気撹拌子を入れ、減圧下で濃縮し、窒素を導入した後、得られた残渣をジクロロメタン5mlにて溶解した。
2 ジホスフィン化合物
3 求電子剤
4 中間生成物
5 ホスフィンボラン
Claims (6)
- ホスフィン化合物におけるリン原子が不斉中心を有する請求項2又は3に記載のビス(ホスフィン)ボロニウム塩の製造方法。
- ホスフィン化合物における置換基のうちの少なくとも一つが、分枝構造を有するアルキル基、環状構造を有するアルキル基、又はアリール基である請求項2ないし4のいずれか1項に記載のジホスフィン化合物の製造方法。
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2007557790A JP5223044B2 (ja) | 2006-02-08 | 2007-01-30 | ビス(ホスフィン)ボロニウム塩、ビス(ホスフィン)ボロニウム塩の製造方法、この製造方法により製造されるビス(ホスフィン)ボロニウム塩 |
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2006030519 | 2006-02-08 | ||
JP2006030519 | 2006-02-08 | ||
PCT/JP2007/051431 WO2007091445A1 (ja) | 2006-02-08 | 2007-01-30 | ビス(ホスフィン)ボロニウム塩、ビス(ホスフィン)ボロニウム塩の製造方法、この製造方法により製造されるビス(ホスフィン)ボロニウム塩 |
JP2007557790A JP5223044B2 (ja) | 2006-02-08 | 2007-01-30 | ビス(ホスフィン)ボロニウム塩、ビス(ホスフィン)ボロニウム塩の製造方法、この製造方法により製造されるビス(ホスフィン)ボロニウム塩 |
Publications (2)
Publication Number | Publication Date |
---|---|
JPWO2007091445A1 JPWO2007091445A1 (ja) | 2009-07-02 |
JP5223044B2 true JP5223044B2 (ja) | 2013-06-26 |
Family
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Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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JP2007557790A Active JP5223044B2 (ja) | 2006-02-08 | 2007-01-30 | ビス(ホスフィン)ボロニウム塩、ビス(ホスフィン)ボロニウム塩の製造方法、この製造方法により製造されるビス(ホスフィン)ボロニウム塩 |
Country Status (5)
Country | Link |
---|---|
US (1) | US7723548B2 (ja) |
EP (1) | EP1982989B1 (ja) |
JP (1) | JP5223044B2 (ja) |
CN (1) | CN101432290A (ja) |
WO (1) | WO2007091445A1 (ja) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2007091446A1 (ja) * | 2006-02-08 | 2007-08-16 | Japan Science And Technology Agency | ジホスフィン化合物の製造方法、この製造方法により製造されるジホスフィン化合物及び中間生成物 |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3839392A (en) * | 1970-04-14 | 1974-10-01 | G Follows | Polyamides |
Family Cites Families (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP4464516B2 (ja) | 2000-03-14 | 2010-05-19 | 日本化学工業株式会社 | ホスフィン・ボラン誘導体の製造方法 |
MXPA02001147A (es) * | 2001-03-19 | 2004-04-21 | Warner Lambert Co | Sintesis de ligandos bisfosina no-c2-simetricos como catalizadores para la hidrogenacion asimetrica. |
JP4271454B2 (ja) | 2002-02-04 | 2009-06-03 | 北興化学工業株式会社 | 嵩高い炭化水素基の結合した第3級ホスフィンの製造方法 |
JP4271455B2 (ja) | 2002-02-19 | 2009-06-03 | 北興化学工業株式会社 | 嵩高い炭化水素基の結合した第3級ホスフィンの製造方法 |
JP4481589B2 (ja) * | 2003-05-06 | 2010-06-16 | 日本曹達株式会社 | ビスホスフィンの製造方法 |
WO2007091446A1 (ja) * | 2006-02-08 | 2007-08-16 | Japan Science And Technology Agency | ジホスフィン化合物の製造方法、この製造方法により製造されるジホスフィン化合物及び中間生成物 |
-
2007
- 2007-01-30 US US12/067,069 patent/US7723548B2/en not_active Expired - Fee Related
- 2007-01-30 EP EP07707662A patent/EP1982989B1/en not_active Expired - Fee Related
- 2007-01-30 WO PCT/JP2007/051431 patent/WO2007091445A1/ja active Application Filing
- 2007-01-30 JP JP2007557790A patent/JP5223044B2/ja active Active
- 2007-01-30 CN CNA200780001621XA patent/CN101432290A/zh active Pending
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3839392A (en) * | 1970-04-14 | 1974-10-01 | G Follows | Polyamides |
Non-Patent Citations (5)
Title |
---|
JPN6012035213; Tetrahedron Letters 45, 2004, pp.9341-9344 * |
JPN7012002604; Tetrahedron 39(4), 1983, pp. 591-597 * |
JPN7012002605; J.Am.Chem.Soc. 121(50), 1999, pp. 11744-11750 * |
JPN7012002606; Angew. Chem. 100(8), 1988, pp. 1135-1138 * |
JPN7012002607; Organic Letters 8(26), 2006, pp. 6103-6106 * |
Also Published As
Publication number | Publication date |
---|---|
EP1982989A4 (en) | 2011-05-18 |
CN101432290A (zh) | 2009-05-13 |
EP1982989A1 (en) | 2008-10-22 |
EP1982989B1 (en) | 2012-08-15 |
WO2007091445A1 (ja) | 2007-08-16 |
US20090062567A1 (en) | 2009-03-05 |
US7723548B2 (en) | 2010-05-25 |
JPWO2007091445A1 (ja) | 2009-07-02 |
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