JP2011526617A5 - - Google Patents
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- Publication number
- JP2011526617A5 JP2011526617A5 JP2011515634A JP2011515634A JP2011526617A5 JP 2011526617 A5 JP2011526617 A5 JP 2011526617A5 JP 2011515634 A JP2011515634 A JP 2011515634A JP 2011515634 A JP2011515634 A JP 2011515634A JP 2011526617 A5 JP2011526617 A5 JP 2011526617A5
- Authority
- JP
- Japan
- Prior art keywords
- tolylphosphinomethyl
- butylphosphinomethyl
- adamantyl
- group
- benzene
- 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
- -1 ethylene, propylene, butylene, isobutylene Chemical group 0.000 claims 103
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims 33
- 229910052698 phosphorus Inorganic materials 0.000 claims 32
- 229910052799 carbon Inorganic materials 0.000 claims 30
- 239000003446 ligand Substances 0.000 claims 28
- KTWOOEGAPBSYNW-UHFFFAOYSA-N ferrocene Chemical compound [Fe+2].C=1C=C[CH-]C=1.C=1C=C[CH-]C=1 KTWOOEGAPBSYNW-UHFFFAOYSA-N 0.000 claims 24
- 125000003118 aryl group Chemical group 0.000 claims 20
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 17
- 125000005073 adamantyl group Chemical group C12(CC3CC(CC(C1)C3)C2)* 0.000 claims 16
- 125000004429 atom Chemical group 0.000 claims 14
- ZJDNAQRUUYRJLW-UHFFFAOYSA-N 2,2,6,6-tetramethylphosphinan-4-one Chemical compound CC1(C)CC(=O)CC(C)(C)P1 ZJDNAQRUUYRJLW-UHFFFAOYSA-N 0.000 claims 12
- 150000001875 compounds Chemical class 0.000 claims 11
- 150000001721 carbon Chemical group 0.000 claims 10
- 230000006315 carbonylation Effects 0.000 claims 10
- 238000005810 carbonylation reaction Methods 0.000 claims 10
- 238000000034 method Methods 0.000 claims 9
- 125000000217 alkyl group Chemical group 0.000 claims 7
- 229910052751 metal Inorganic materials 0.000 claims 7
- 239000002184 metal Substances 0.000 claims 7
- 125000000026 trimethylsilyl group Chemical group [H]C([H])([H])[Si]([*])(C([H])([H])[H])C([H])([H])[H] 0.000 claims 6
- 239000003054 catalyst Substances 0.000 claims 5
- DOUYOVFHQKVSSJ-UHFFFAOYSA-N [Fe].c1cccc1.CC(C)(C)c1cccc1 Chemical compound [Fe].c1cccc1.CC(C)(C)c1cccc1 DOUYOVFHQKVSSJ-UHFFFAOYSA-N 0.000 claims 4
- 125000005647 linker group Chemical group 0.000 claims 4
- 125000001424 substituent group Chemical group 0.000 claims 4
- IHOMKOPTBSYOCI-UHFFFAOYSA-N [Fe].c1cccc1.c1ccc(c1)C1=CC=CC=C1 Chemical compound [Fe].c1cccc1.c1ccc(c1)C1=CC=CC=C1 IHOMKOPTBSYOCI-UHFFFAOYSA-N 0.000 claims 3
- 239000002253 acid Substances 0.000 claims 3
- 125000001931 aliphatic group Chemical group 0.000 claims 3
- IBXNCJKFFQIKKY-UHFFFAOYSA-N 1-pentyne Chemical group CCCC#C IBXNCJKFFQIKKY-UHFFFAOYSA-N 0.000 claims 2
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 claims 2
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims 2
- 239000005977 Ethylene Substances 0.000 claims 2
- XYFCBTPGUUZFHI-UHFFFAOYSA-N Phosphine Chemical compound P XYFCBTPGUUZFHI-UHFFFAOYSA-N 0.000 claims 2
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims 2
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims 2
- 125000002947 alkylene group Chemical group 0.000 claims 2
- 229910052787 antimony Inorganic materials 0.000 claims 2
- WATWJIUSRGPENY-UHFFFAOYSA-N antimony atom Chemical compound [Sb] WATWJIUSRGPENY-UHFFFAOYSA-N 0.000 claims 2
- 229910052785 arsenic Inorganic materials 0.000 claims 2
- RQNWIZPPADIBDY-UHFFFAOYSA-N arsenic atom Chemical compound [As] RQNWIZPPADIBDY-UHFFFAOYSA-N 0.000 claims 2
- 125000004432 carbon atom Chemical group C* 0.000 claims 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 2
- 229910052739 hydrogen Inorganic materials 0.000 claims 2
- 239000001257 hydrogen Substances 0.000 claims 2
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims 2
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 2
- 150000002736 metal compounds Chemical class 0.000 claims 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 2
- ZGEGCLOFRBLKSE-UHFFFAOYSA-N methylene hexane Natural products CCCCCC=C ZGEGCLOFRBLKSE-UHFFFAOYSA-N 0.000 claims 2
- 125000003261 o-tolyl group Chemical group [H]C1=C([H])C(*)=C(C([H])=C1[H])C([H])([H])[H] 0.000 claims 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 2
- 239000011574 phosphorus Substances 0.000 claims 2
- CRSBERNSMYQZNG-UHFFFAOYSA-N 1 -dodecene Natural products CCCCCCCCCCC=C CRSBERNSMYQZNG-UHFFFAOYSA-N 0.000 claims 1
- KWKAKUADMBZCLK-UHFFFAOYSA-N 1-octene Chemical compound CCCCCCC=C KWKAKUADMBZCLK-UHFFFAOYSA-N 0.000 claims 1
- DSNOMSXWRCNIHI-UHFFFAOYSA-N C(C)(C)(C)P(C(C)(C)C)CC1=C(C=C(C=C1)C(C)(C)C)CP(C1=C(C=CC=C1)C)C1=C(C=CC=C1)C.C(C)(C)(C)P(C(C)(C)C)CC1=C(C=C(C(=C1)C(C)(C)C)C(C)(C)C)CP(C1=C(C=CC=C1)C)C1=C(C=CC=C1)C Chemical compound C(C)(C)(C)P(C(C)(C)C)CC1=C(C=C(C=C1)C(C)(C)C)CP(C1=C(C=CC=C1)C)C1=C(C=CC=C1)C.C(C)(C)(C)P(C(C)(C)C)CC1=C(C=C(C(=C1)C(C)(C)C)C(C)(C)C)CP(C1=C(C=CC=C1)C)C1=C(C=CC=C1)C DSNOMSXWRCNIHI-UHFFFAOYSA-N 0.000 claims 1
- HVMPVPAQZWAOAN-UHFFFAOYSA-N C(C)(C)(C)P(C(C)(C)C)CC1=C(C=C(C=C1)[Si](C)(C)C)CP(C1=C(C=CC=C1)C)C1=C(C=CC=C1)C.C(C)(C)(C)P(C(C)(C)C)CC1=C(C=C(C(=C1)[Si](C)(C)C)[Si](C)(C)C)CP(C1=C(C=CC=C1)C)C1=C(C=CC=C1)C Chemical compound C(C)(C)(C)P(C(C)(C)C)CC1=C(C=C(C=C1)[Si](C)(C)C)CP(C1=C(C=CC=C1)C)C1=C(C=CC=C1)C.C(C)(C)(C)P(C(C)(C)C)CC1=C(C=C(C(=C1)[Si](C)(C)C)[Si](C)(C)C)CP(C1=C(C=CC=C1)C)C1=C(C=CC=C1)C HVMPVPAQZWAOAN-UHFFFAOYSA-N 0.000 claims 1
- YFWPBDWXSGGNJJ-UHFFFAOYSA-N C(C)(C)(C)P(C(C)(C)C)C[C-]1C(=CC(=C1C1=CC=CC=C1)C1=CC=CC=C1)CP(C1=C(C=CC=C1)C)C1=C(C=CC=C1)C.[CH-]1C=CC=C1.[Fe+2] Chemical compound C(C)(C)(C)P(C(C)(C)C)C[C-]1C(=CC(=C1C1=CC=CC=C1)C1=CC=CC=C1)CP(C1=C(C=CC=C1)C)C1=C(C=CC=C1)C.[CH-]1C=CC=C1.[Fe+2] YFWPBDWXSGGNJJ-UHFFFAOYSA-N 0.000 claims 1
- HOCOZEDSTIJTFP-UHFFFAOYSA-N C12(CC3CC(CC(C1)C3)C2)P(C23CC1CC(CC(C2)C1)C3)C[C-]3C(=CC(=C3C3=CC=CC=C3)C3=CC=CC=C3)CP(C3=C(C=CC=C3)C)C3=C(C=CC=C3)C.[CH-]3C=CC=C3.[Fe+2] Chemical compound C12(CC3CC(CC(C1)C3)C2)P(C23CC1CC(CC(C2)C1)C3)C[C-]3C(=CC(=C3C3=CC=CC=C3)C3=CC=CC=C3)CP(C3=C(C=CC=C3)C)C3=C(C=CC=C3)C.[CH-]3C=CC=C3.[Fe+2] HOCOZEDSTIJTFP-UHFFFAOYSA-N 0.000 claims 1
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 claims 1
- SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 claims 1
- RFZRIQOILFQQDZ-UHFFFAOYSA-N PCC1C2(CC3CC(CC1C3)C2)[C-]2C(=CC(=C2C2=CC=CC=C2)C2=CC=CC=C2)CP(C2=C(C=CC=C2)C)C2=C(C=CC=C2)C.[CH-]2C=CC=C2.[Fe+2] Chemical compound PCC1C2(CC3CC(CC1C3)C2)[C-]2C(=CC(=C2C2=CC=CC=C2)C2=CC=CC=C2)CP(C2=C(C=CC=C2)C)C2=C(C=CC=C2)C.[CH-]2C=CC=C2.[Fe+2] RFZRIQOILFQQDZ-UHFFFAOYSA-N 0.000 claims 1
- WPHPHEZWJGHIJW-UHFFFAOYSA-N [2-[bis(2-methylphenyl)phosphanylmethyl]-4,5-diphenylphenyl]methyl-ditert-butylphosphane Chemical compound CC1=CC=CC=C1P(C=1C(=CC=CC=1)C)CC1=CC(C=2C=CC=CC=2)=C(C=2C=CC=CC=2)C=C1CP(C(C)(C)C)C(C)(C)C WPHPHEZWJGHIJW-UHFFFAOYSA-N 0.000 claims 1
- MDJCAYKPZXLNBF-UHFFFAOYSA-N [2-[bis(2-methylphenyl)phosphanylmethyl]naphthalen-1-yl]methyl-ditert-butylphosphane Chemical compound CC1=CC=CC=C1P(C=1C(=CC=CC=1)C)CC1=CC=C(C=CC=C2)C2=C1CP(C(C)(C)C)C(C)(C)C MDJCAYKPZXLNBF-UHFFFAOYSA-N 0.000 claims 1
- HZLVXIYQPCBKRV-UHFFFAOYSA-N [2-[bis(2-methylphenyl)phosphanylmethyl]phenyl]methyl-ditert-butylphosphane Chemical compound CC1=CC=CC=C1P(C=1C(=CC=CC=1)C)CC1=CC=CC=C1CP(C(C)(C)C)C(C)(C)C HZLVXIYQPCBKRV-UHFFFAOYSA-N 0.000 claims 1
- YTLHCDPLQJEQAK-UHFFFAOYSA-N [4,5-diphenyl-2-[2-(phosphanylmethyl)-1-adamantyl]phenyl]methyl-bis(2-methylphenyl)phosphane Chemical compound CC1=CC=CC=C1P(C=1C(=CC=CC=1)C)CC1=CC(C=2C=CC=CC=2)=C(C=2C=CC=CC=2)C=C1C1(C2)C(CP)C(C3)CC2CC3C1 YTLHCDPLQJEQAK-UHFFFAOYSA-N 0.000 claims 1
- RPJPEZDOKLWUJU-UHFFFAOYSA-N [5-tert-butyl-2-[2-(phosphanylmethyl)-1-adamantyl]phenyl]methyl-bis(2-methylphenyl)phosphane Chemical compound CC1=CC=CC=C1P(C=1C(=CC=CC=1)C)CC1=CC(C(C)(C)C)=CC=C1C1(C2)C(CP)C(C3)CC2CC3C1 RPJPEZDOKLWUJU-UHFFFAOYSA-N 0.000 claims 1
- 125000003342 alkenyl group Chemical group 0.000 claims 1
- 125000000304 alkynyl group Chemical group 0.000 claims 1
- YIYBQIKDCADOSF-UHFFFAOYSA-N alpha-Butylen-alpha-carbonsaeure Natural products CCC=CC(O)=O YIYBQIKDCADOSF-UHFFFAOYSA-N 0.000 claims 1
- HSFWRNGVRCDJHI-UHFFFAOYSA-N alpha-acetylene Natural products C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 0.000 claims 1
- 150000001450 anions Chemical class 0.000 claims 1
- 229910000074 antimony hydride Inorganic materials 0.000 claims 1
- RBFQJDQYXXHULB-UHFFFAOYSA-N arsane Chemical compound [AsH3] RBFQJDQYXXHULB-UHFFFAOYSA-N 0.000 claims 1
- YHGRMOSTMBFKJG-UHFFFAOYSA-N benzyl-bis(2-methylphenyl)phosphane Chemical compound CC1=CC=CC=C1P(C=1C(=CC=CC=1)C)CC1=CC=CC=C1 YHGRMOSTMBFKJG-UHFFFAOYSA-N 0.000 claims 1
- AIMFFXUBKIDAKE-UHFFFAOYSA-N bis(1-adamantyl)-[[2-[bis(2-methylphenyl)phosphanylmethyl]-4,5-bis(trimethylsilyl)phenyl]methyl]phosphane Chemical compound CC1=CC=CC=C1P(C=1C(=CC=CC=1)C)CC1=CC([Si](C)(C)C)=C([Si](C)(C)C)C=C1CP(C12CC3CC(CC(C3)C1)C2)C1(C2)CC(C3)CC2CC3C1 AIMFFXUBKIDAKE-UHFFFAOYSA-N 0.000 claims 1
- JZPCBFNJBCVJBS-UHFFFAOYSA-N bis(1-adamantyl)-[[2-[bis(2-methylphenyl)phosphanylmethyl]-4,5-diphenylphenyl]methyl]phosphane Chemical compound CC1=CC=CC=C1P(C=1C(=CC=CC=1)C)CC1=CC(C=2C=CC=CC=2)=C(C=2C=CC=CC=2)C=C1CP(C12CC3CC(CC(C3)C1)C2)C1(C2)CC(C3)CC2CC3C1 JZPCBFNJBCVJBS-UHFFFAOYSA-N 0.000 claims 1
- YOLJDCZYSKGCKB-UHFFFAOYSA-N bis(1-adamantyl)-[[2-[bis(2-methylphenyl)phosphanylmethyl]-4-tert-butylphenyl]methyl]phosphane Chemical compound CC1=CC=CC=C1P(C=1C(=CC=CC=1)C)CC1=CC(C(C)(C)C)=CC=C1CP(C12CC3CC(CC(C3)C1)C2)C1(C2)CC(C3)CC2CC3C1 YOLJDCZYSKGCKB-UHFFFAOYSA-N 0.000 claims 1
- TWBHUYHOFWDPFP-UHFFFAOYSA-N bis(2-methylphenyl)-[[2-[2-(phosphanylmethyl)-1-adamantyl]-4,5-bis(trimethylsilyl)phenyl]methyl]phosphane Chemical compound CC1=CC=CC=C1P(C=1C(=CC=CC=1)C)CC1=CC([Si](C)(C)C)=C([Si](C)(C)C)C=C1C1(C2)C(CP)C(C3)CC2CC3C1 TWBHUYHOFWDPFP-UHFFFAOYSA-N 0.000 claims 1
- ACECABFVIYERKA-UHFFFAOYSA-N bis(2-methylphenyl)-[[2-[2-(phosphanylmethyl)-1-adamantyl]-5-trimethylsilylphenyl]methyl]phosphane Chemical compound CC1=CC=CC=C1P(C=1C(=CC=CC=1)C)CC1=CC([Si](C)(C)C)=CC=C1C1(C2)C(CP)C(C3)CC2CC3C1 ACECABFVIYERKA-UHFFFAOYSA-N 0.000 claims 1
- NUXRXJINZITJTG-UHFFFAOYSA-N bis(2-methylphenyl)-[[5-phenyl-2-[2-(phosphanylmethyl)-1-adamantyl]phenyl]methyl]phosphane Chemical compound CC1=CC=CC=C1P(C=1C(=CC=CC=1)C)CC1=CC(C=2C=CC=CC=2)=CC=C1C1(C2)C(CP)C(C3)CC2CC3C1 NUXRXJINZITJTG-UHFFFAOYSA-N 0.000 claims 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims 1
- 229910021386 carbon form Inorganic materials 0.000 claims 1
- 229910002091 carbon monoxide Inorganic materials 0.000 claims 1
- 239000002131 composite material Substances 0.000 claims 1
- 125000004093 cyano group Chemical group *C#N 0.000 claims 1
- VWSZKFRVIOXRFP-UHFFFAOYSA-N cyclopenta-1,3-diene iron(2+) (2-methylcyclopenta-2,4-dien-1-yl)benzene Chemical compound [Fe++].c1cc[cH-]c1.Cc1ccc[c-]1-c1ccccc1 VWSZKFRVIOXRFP-UHFFFAOYSA-N 0.000 claims 1
- 229940069096 dodecene Drugs 0.000 claims 1
- 125000005677 ethinylene group Chemical group [*:2]C#C[*:1] 0.000 claims 1
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 claims 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 claims 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims 1
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 claims 1
- 239000000203 mixture Substances 0.000 claims 1
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 claims 1
- 125000001971 neopentyl group Chemical group [H]C([*])([H])C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H] 0.000 claims 1
- 125000000962 organic group Chemical group 0.000 claims 1
- ISBHMJZRKAFTGE-UHFFFAOYSA-N pent-2-enenitrile Chemical compound CCC=CC#N ISBHMJZRKAFTGE-UHFFFAOYSA-N 0.000 claims 1
- 125000003538 pentan-3-yl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])C([H])([H])[H] 0.000 claims 1
- YWAKXRMUMFPDSH-UHFFFAOYSA-N pentene Chemical compound CCCC=C YWAKXRMUMFPDSH-UHFFFAOYSA-N 0.000 claims 1
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 claims 1
- 229910000073 phosphorus hydride Inorganic materials 0.000 claims 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims 1
- MWWATHDPGQKSAR-UHFFFAOYSA-N propyne Chemical group CC#C MWWATHDPGQKSAR-UHFFFAOYSA-N 0.000 claims 1
- 125000006413 ring segment Chemical group 0.000 claims 1
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 1
- OUULRIDHGPHMNQ-UHFFFAOYSA-N stibane Chemical compound [SbH3] OUULRIDHGPHMNQ-UHFFFAOYSA-N 0.000 claims 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims 1
- YIYBQIKDCADOSF-ONEGZZNKSA-N trans-pent-2-enoic acid Chemical compound CC\C=C\C(O)=O YIYBQIKDCADOSF-ONEGZZNKSA-N 0.000 claims 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GBGB0812297.0A GB0812297D0 (en) | 2008-07-04 | 2008-07-04 | Novel carbonylation ligand sand thier use of in the carbonylation of ethylenically unsaturated compounds |
| GB0812297.0 | 2008-07-04 | ||
| PCT/GB2009/050780 WO2010001174A1 (en) | 2008-07-04 | 2009-07-02 | Process for the carbonylation of ethylenically unsaturated compounds, novel carbonylation ligands and catalyst systems incorporating such ligands |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2014212569A Division JP2015017127A (ja) | 2008-07-04 | 2014-10-17 | エチレン性不飽和化合物のカルボニル化法、新規なカルボニル化配位子およびかかる配位子を組み入れた触媒系 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2011526617A JP2011526617A (ja) | 2011-10-13 |
| JP2011526617A5 true JP2011526617A5 (enExample) | 2012-08-16 |
| JP5711120B2 JP5711120B2 (ja) | 2015-04-30 |
Family
ID=39718006
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2011515634A Expired - Fee Related JP5711120B2 (ja) | 2008-07-04 | 2009-07-02 | エチレン性不飽和化合物のカルボニル化法、新規なカルボニル化配位子およびかかる配位子を組み入れた触媒系 |
| JP2014212569A Pending JP2015017127A (ja) | 2008-07-04 | 2014-10-17 | エチレン性不飽和化合物のカルボニル化法、新規なカルボニル化配位子およびかかる配位子を組み入れた触媒系 |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2014212569A Pending JP2015017127A (ja) | 2008-07-04 | 2014-10-17 | エチレン性不飽和化合物のカルボニル化法、新規なカルボニル化配位子およびかかる配位子を組み入れた触媒系 |
Country Status (17)
| Country | Link |
|---|---|
| US (1) | US8816113B2 (enExample) |
| EP (1) | EP2297170B1 (enExample) |
| JP (2) | JP5711120B2 (enExample) |
| KR (1) | KR101632375B1 (enExample) |
| CN (2) | CN102083842A (enExample) |
| AU (1) | AU2009265367B2 (enExample) |
| BR (1) | BRPI0914105B1 (enExample) |
| CA (1) | CA2727163C (enExample) |
| EA (1) | EA023307B1 (enExample) |
| ES (1) | ES2555977T3 (enExample) |
| GB (1) | GB0812297D0 (enExample) |
| MX (1) | MX2010014404A (enExample) |
| MY (1) | MY178676A (enExample) |
| SG (1) | SG192476A1 (enExample) |
| TW (1) | TWI488691B (enExample) |
| WO (1) | WO2010001174A1 (enExample) |
| ZA (1) | ZA201009103B (enExample) |
Families Citing this family (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB0812297D0 (en) * | 2008-07-04 | 2008-08-13 | Lucite Int Uk Ltd | Novel carbonylation ligand sand thier use of in the carbonylation of ethylenically unsaturated compounds |
| GB201000078D0 (en) | 2010-01-05 | 2010-02-17 | Lucite Int Uk Ltd | Process for the carbonylation of ethylenically unsaturated compounds, novel carbonylation ligands and catalyst systems incorporatng such ligands |
| EP3441384B1 (de) * | 2017-08-08 | 2019-12-25 | Evonik Operations GmbH | Methoxycarbonylierung mit ameisensäure und methanol |
| EP3441383B1 (de) | 2017-08-08 | 2019-12-25 | Evonik Operations GmbH | Methoxycarbonylierung mit ameisensäure als co-quelle |
| GB201714756D0 (en) * | 2017-09-13 | 2017-10-25 | Lucite Int Uk Ltd | A catalyst and a process for the production of ethylenicallly unsaturated carboxylic acids or esters |
| AR121356A1 (es) | 2020-02-18 | 2022-05-11 | Gilead Sciences Inc | Compuestos antivirales |
| TWI874791B (zh) | 2020-02-18 | 2025-03-01 | 美商基利科學股份有限公司 | 抗病毒化合物 |
| TWI883391B (zh) | 2020-02-18 | 2025-05-11 | 美商基利科學股份有限公司 | 抗病毒化合物 |
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2009
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- 2009-07-02 WO PCT/GB2009/050780 patent/WO2010001174A1/en not_active Ceased
- 2009-07-02 CA CA2727163A patent/CA2727163C/en active Active
- 2009-07-02 SG SG2013052006A patent/SG192476A1/en unknown
- 2009-07-02 MY MYPI2011000006A patent/MY178676A/en unknown
- 2009-07-02 US US13/002,406 patent/US8816113B2/en active Active
- 2009-07-02 ES ES09772854.7T patent/ES2555977T3/es active Active
- 2009-07-02 MX MX2010014404A patent/MX2010014404A/es active IP Right Grant
- 2009-07-02 KR KR1020117002329A patent/KR101632375B1/ko not_active Expired - Fee Related
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