JP2010509393A5 - - Google Patents
Download PDFInfo
- Publication number
- JP2010509393A5 JP2010509393A5 JP2009536823A JP2009536823A JP2010509393A5 JP 2010509393 A5 JP2010509393 A5 JP 2010509393A5 JP 2009536823 A JP2009536823 A JP 2009536823A JP 2009536823 A JP2009536823 A JP 2009536823A JP 2010509393 A5 JP2010509393 A5 JP 2010509393A5
- Authority
- JP
- Japan
- Prior art keywords
- compound
- formula
- substrate
- aryl
- alkyl
- 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.)
- Pending
Links
- 150000001875 compounds Chemical class 0.000 claims description 79
- 125000003118 aryl group Chemical group 0.000 claims description 48
- 125000000217 alkyl group Chemical group 0.000 claims description 47
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 39
- 239000000203 mixture Substances 0.000 claims description 39
- 238000000034 method Methods 0.000 claims description 34
- -1 perfluoro Chemical group 0.000 claims description 29
- 239000000758 substrate Substances 0.000 claims description 29
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical group [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 12
- 229910052717 sulfur Inorganic materials 0.000 claims description 11
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 10
- 229910052760 oxygen Inorganic materials 0.000 claims description 9
- XYFCBTPGUUZFHI-UHFFFAOYSA-N Phosphine Chemical compound P XYFCBTPGUUZFHI-UHFFFAOYSA-N 0.000 claims description 7
- 239000003054 catalyst Substances 0.000 claims description 7
- 229910052698 phosphorus Inorganic materials 0.000 claims description 7
- 229910052782 aluminium Inorganic materials 0.000 claims description 6
- 229910052796 boron Inorganic materials 0.000 claims description 6
- 229910052733 gallium Inorganic materials 0.000 claims description 6
- 125000001424 substituent group Chemical group 0.000 claims description 6
- 238000006243 chemical reaction Methods 0.000 claims description 5
- 229910052757 nitrogen Inorganic materials 0.000 claims description 5
- 239000002904 solvent Substances 0.000 claims description 5
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 4
- 229910000073 phosphorus hydride Inorganic materials 0.000 claims description 4
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims description 3
- 239000012530 fluid Substances 0.000 claims description 3
- 239000002841 Lewis acid Substances 0.000 claims description 2
- 239000002879 Lewis base Substances 0.000 claims description 2
- 150000007527 lewis bases Chemical class 0.000 claims description 2
- 229910052719 titanium Inorganic materials 0.000 claims description 2
- 229910052726 zirconium Inorganic materials 0.000 claims description 2
- 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 8
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical group CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims 7
- 239000003153 chemical reaction reagent Substances 0.000 claims 6
- 238000006467 substitution reaction Methods 0.000 claims 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims 3
- 229940125904 compound 1 Drugs 0.000 claims 3
- 229940125782 compound 2 Drugs 0.000 claims 3
- 238000001914 filtration Methods 0.000 claims 3
- SZUVGFMDDVSKSI-WIFOCOSTSA-N (1s,2s,3s,5r)-1-(carboxymethyl)-3,5-bis[(4-phenoxyphenyl)methyl-propylcarbamoyl]cyclopentane-1,2-dicarboxylic acid Chemical compound O=C([C@@H]1[C@@H]([C@](CC(O)=O)([C@H](C(=O)N(CCC)CC=2C=CC(OC=3C=CC=CC=3)=CC=2)C1)C(O)=O)C(O)=O)N(CCC)CC(C=C1)=CC=C1OC1=CC=CC=C1 SZUVGFMDDVSKSI-WIFOCOSTSA-N 0.000 claims 2
- BHAJUXABDQWRKH-WCRBZPEASA-N (2s,3r)-1,2,3-triphenylaziridine Chemical group C1=CC=CC=C1[C@@H]1N(C=2C=CC=CC=2)[C@@H]1C1=CC=CC=C1 BHAJUXABDQWRKH-WCRBZPEASA-N 0.000 claims 2
- 239000004215 Carbon black (E152) Substances 0.000 claims 2
- RRSNDVCODIMOFX-MPKOGUQCSA-N Fc1c(Cl)cccc1[C@H]1[C@@H](NC2(CCCCC2)[C@@]11C(=O)Nc2cc(Cl)ccc12)C(=O)Nc1ccc(cc1)C(=O)NCCCCCc1cccc2C(=O)N(Cc12)C1CCC(=O)NC1=O Chemical compound Fc1c(Cl)cccc1[C@H]1[C@@H](NC2(CCCCC2)[C@@]11C(=O)Nc2cc(Cl)ccc12)C(=O)Nc1ccc(cc1)C(=O)NCCCCCc1cccc2C(=O)N(Cc12)C1CCC(=O)NC1=O RRSNDVCODIMOFX-MPKOGUQCSA-N 0.000 claims 2
- 229940126543 compound 14 Drugs 0.000 claims 2
- 125000001153 fluoro group Chemical group F* 0.000 claims 2
- 229930195733 hydrocarbon Natural products 0.000 claims 2
- FKURONBIQLIBEN-UHFFFAOYSA-N n-(1,2-diphenylethyl)aniline Chemical group C=1C=CC=CC=1CC(C=1C=CC=CC=1)NC1=CC=CC=C1 FKURONBIQLIBEN-UHFFFAOYSA-N 0.000 claims 2
- GLGNXYJARSMNGJ-VKTIVEEGSA-N (1s,2s,3r,4r)-3-[[5-chloro-2-[(1-ethyl-6-methoxy-2-oxo-4,5-dihydro-3h-1-benzazepin-7-yl)amino]pyrimidin-4-yl]amino]bicyclo[2.2.1]hept-5-ene-2-carboxamide Chemical compound CCN1C(=O)CCCC2=C(OC)C(NC=3N=C(C(=CN=3)Cl)N[C@H]3[C@H]([C@@]4([H])C[C@@]3(C=C4)[H])C(N)=O)=CC=C21 GLGNXYJARSMNGJ-VKTIVEEGSA-N 0.000 claims 1
- GHYOCDFICYLMRF-UTIIJYGPSA-N (2S,3R)-N-[(2S)-3-(cyclopenten-1-yl)-1-[(2R)-2-methyloxiran-2-yl]-1-oxopropan-2-yl]-3-hydroxy-3-(4-methoxyphenyl)-2-[[(2S)-2-[(2-morpholin-4-ylacetyl)amino]propanoyl]amino]propanamide Chemical compound C1(=CCCC1)C[C@@H](C(=O)[C@@]1(OC1)C)NC([C@H]([C@@H](C1=CC=C(C=C1)OC)O)NC([C@H](C)NC(CN1CCOCC1)=O)=O)=O GHYOCDFICYLMRF-UTIIJYGPSA-N 0.000 claims 1
- QFLWZFQWSBQYPS-AWRAUJHKSA-N (3S)-3-[[(2S)-2-[[(2S)-2-[5-[(3aS,6aR)-2-oxo-1,3,3a,4,6,6a-hexahydrothieno[3,4-d]imidazol-4-yl]pentanoylamino]-3-methylbutanoyl]amino]-3-(4-hydroxyphenyl)propanoyl]amino]-4-[1-bis(4-chlorophenoxy)phosphorylbutylamino]-4-oxobutanoic acid Chemical compound CCCC(NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)CCCCC1SC[C@@H]2NC(=O)N[C@H]12)C(C)C)P(=O)(Oc1ccc(Cl)cc1)Oc1ccc(Cl)cc1 QFLWZFQWSBQYPS-AWRAUJHKSA-N 0.000 claims 1
- ONBQEOIKXPHGMB-VBSBHUPXSA-N 1-[2-[(2s,3r,4s,5r)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy-4,6-dihydroxyphenyl]-3-(4-hydroxyphenyl)propan-1-one Chemical compound O[C@@H]1[C@H](O)[C@@H](CO)O[C@H]1OC1=CC(O)=CC(O)=C1C(=O)CCC1=CC=C(O)C=C1 ONBQEOIKXPHGMB-VBSBHUPXSA-N 0.000 claims 1
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 claims 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims 1
- 238000007259 addition reaction Methods 0.000 claims 1
- 150000001299 aldehydes Chemical class 0.000 claims 1
- HSFWRNGVRCDJHI-UHFFFAOYSA-N alpha-acetylene Natural products C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 0.000 claims 1
- BGECDVWSWDRFSP-UHFFFAOYSA-N borazine Chemical compound B1NBNBN1 BGECDVWSWDRFSP-UHFFFAOYSA-N 0.000 claims 1
- 229910052799 carbon Inorganic materials 0.000 claims 1
- 229940125797 compound 12 Drugs 0.000 claims 1
- 229940125758 compound 15 Drugs 0.000 claims 1
- 229940126142 compound 16 Drugs 0.000 claims 1
- 238000004821 distillation Methods 0.000 claims 1
- 150000002085 enols Chemical class 0.000 claims 1
- 150000002118 epoxides Chemical class 0.000 claims 1
- 150000002148 esters Chemical class 0.000 claims 1
- CCGKOQOJPYTBIH-UHFFFAOYSA-N ethenone Chemical compound C=C=O CCGKOQOJPYTBIH-UHFFFAOYSA-N 0.000 claims 1
- 238000000605 extraction Methods 0.000 claims 1
- 238000011049 filling Methods 0.000 claims 1
- 238000010438 heat treatment Methods 0.000 claims 1
- 229910052738 indium Inorganic materials 0.000 claims 1
- 150000002576 ketones Chemical class 0.000 claims 1
- 150000007517 lewis acids Chemical class 0.000 claims 1
- 125000005647 linker group Chemical group 0.000 claims 1
- 239000007788 liquid Substances 0.000 claims 1
- 238000002156 mixing Methods 0.000 claims 1
- DLSOILHAKCBARI-UHFFFAOYSA-N n-benzyl-2-methylpropan-2-amine Chemical compound CC(C)(C)NCC1=CC=CC=C1 DLSOILHAKCBARI-UHFFFAOYSA-N 0.000 claims 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 claims 1
- 239000011574 phosphorus Substances 0.000 claims 1
- 150000003141 primary amines Chemical class 0.000 claims 1
- 150000003335 secondary amines Chemical class 0.000 claims 1
- 239000000377 silicon dioxide Substances 0.000 claims 1
- 150000003573 thiols Chemical group 0.000 claims 1
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
- 229910052739 hydrogen Inorganic materials 0.000 description 6
- UORVGPXVDQYIDP-UHFFFAOYSA-N borane Chemical compound B UORVGPXVDQYIDP-UHFFFAOYSA-N 0.000 description 4
- 239000001257 hydrogen Substances 0.000 description 4
- 239000000047 product Substances 0.000 description 3
- OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 2
- 229910000085 borane Inorganic materials 0.000 description 2
- 238000009903 catalytic hydrogenation reaction Methods 0.000 description 2
- 238000005984 hydrogenation reaction Methods 0.000 description 2
- 239000002244 precipitate Substances 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- YBYIRNPNPLQARY-UHFFFAOYSA-N 1H-indene Natural products C1=CC=C2CC=CC2=C1 YBYIRNPNPLQARY-UHFFFAOYSA-N 0.000 description 1
- FKLJPTJMIBLJAV-UHFFFAOYSA-N Compound IV Chemical compound O1N=C(C)C=C1CCCCCCCOC1=CC=C(C=2OCCN=2)C=C1 FKLJPTJMIBLJAV-UHFFFAOYSA-N 0.000 description 1
- GYHNNYVSQQEPJS-UHFFFAOYSA-N Gallium Chemical compound [Ga] GYHNNYVSQQEPJS-UHFFFAOYSA-N 0.000 description 1
- 150000004703 alkoxides Chemical class 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- SLLGVCUQYRMELA-UHFFFAOYSA-N chlorosilicon Chemical compound Cl[Si] SLLGVCUQYRMELA-UHFFFAOYSA-N 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 229940125773 compound 10 Drugs 0.000 description 1
- 229940126214 compound 3 Drugs 0.000 description 1
- 229940125898 compound 5 Drugs 0.000 description 1
- 125000000058 cyclopentadienyl group Chemical group C1(=CC=CC1)* 0.000 description 1
- ZSWFCLXCOIISFI-UHFFFAOYSA-N endo-cyclopentadiene Natural products C1C=CC=C1 ZSWFCLXCOIISFI-UHFFFAOYSA-N 0.000 description 1
- NLFBCYMMUAKCPC-KQQUZDAGSA-N ethyl (e)-3-[3-amino-2-cyano-1-[(e)-3-ethoxy-3-oxoprop-1-enyl]sulfanyl-3-oxoprop-1-enyl]sulfanylprop-2-enoate Chemical compound CCOC(=O)\C=C\SC(=C(C#N)C(N)=O)S\C=C\C(=O)OCC NLFBCYMMUAKCPC-KQQUZDAGSA-N 0.000 description 1
- 125000003983 fluorenyl group Chemical group C1(=CC=CC=2C3=CC=CC=C3CC12)* 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 125000003454 indenyl group Chemical group C1(C=CC2=CC=CC=C12)* 0.000 description 1
- 150000002471 indium Chemical class 0.000 description 1
- ZLVXBBHTMQJRSX-VMGNSXQWSA-N jdtic Chemical compound C1([C@]2(C)CCN(C[C@@H]2C)C[C@H](C(C)C)NC(=O)[C@@H]2NCC3=CC(O)=CC=C3C2)=CC=CC(O)=C1 ZLVXBBHTMQJRSX-VMGNSXQWSA-N 0.000 description 1
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- 230000000269 nucleophilic effect Effects 0.000 description 1
- 239000001301 oxygen Chemical group 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-M phenolate Chemical compound [O-]C1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-M 0.000 description 1
- 150000003003 phosphines Chemical class 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 150000003463 sulfur Chemical group 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 239000003039 volatile agent Substances 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US86568406P | 2006-11-14 | 2006-11-14 | |
| US89655707P | 2007-03-23 | 2007-03-23 | |
| PCT/IB2007/004577 WO2008125911A2 (en) | 2006-11-14 | 2007-11-14 | Hydrogen splitting composition |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2010509393A JP2010509393A (ja) | 2010-03-25 |
| JP2010509393A5 true JP2010509393A5 (cg-RX-API-DMAC7.html) | 2012-01-12 |
Family
ID=39864421
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2009536823A Pending JP2010509393A (ja) | 2006-11-14 | 2007-11-14 | 水素開裂組成物 |
Country Status (10)
| Country | Link |
|---|---|
| US (2) | US8299284B2 (cg-RX-API-DMAC7.html) |
| EP (1) | EP2091957A4 (cg-RX-API-DMAC7.html) |
| JP (1) | JP2010509393A (cg-RX-API-DMAC7.html) |
| KR (1) | KR20090078835A (cg-RX-API-DMAC7.html) |
| CN (1) | CN102066390A (cg-RX-API-DMAC7.html) |
| AU (1) | AU2007350983A1 (cg-RX-API-DMAC7.html) |
| CA (1) | CA2669545C (cg-RX-API-DMAC7.html) |
| MX (1) | MX2009005127A (cg-RX-API-DMAC7.html) |
| SG (1) | SG176482A1 (cg-RX-API-DMAC7.html) |
| WO (1) | WO2008125911A2 (cg-RX-API-DMAC7.html) |
Families Citing this family (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP2928600B1 (en) | 2012-12-07 | 2024-02-21 | University of Central Florida Research Foundation, Inc. | Heterogeneously catalyzed chemical reduction of carbon dioxide |
| CA2894146A1 (en) * | 2012-12-07 | 2014-06-12 | University Of Central Florida Research Foundation, Inc. | Heterogeneous metal-free catalyst |
| GB2522858A (en) * | 2014-02-05 | 2015-08-12 | Imp Innovations Ltd | Fuel cell and battery |
| WO2016097734A1 (en) * | 2014-12-16 | 2016-06-23 | Isis Innovation Limited | Solid-phase catalysts comprising supported frustrated lewis pairs |
| WO2016167981A1 (en) | 2015-04-13 | 2016-10-20 | Garmor Inc. | Graphite oxide reinforced fiber in hosts such as concrete or asphalt |
| US10988488B2 (en) | 2015-04-23 | 2021-04-27 | UNIVERSITé LAVAL | Process for the functionalization of sp2-H carbons using frustrated lewis pair catalysts |
| EP3389859A4 (en) * | 2015-12-15 | 2019-12-11 | Université Laval | Precatalysts and method for the metal-free functionalization of SP2 carbons with it |
| US10821429B2 (en) | 2015-12-15 | 2020-11-03 | UNIVERSITé LAVAL | Precatalysts and process for the metal-free functionalization of SP2 carbons using the same |
| JP7079696B2 (ja) * | 2018-08-29 | 2022-06-02 | 株式会社日本触媒 | ホウ素化合物、およびそれを用いた水素化物、重合体ならびに付加体の製造方法 |
| KR20220016906A (ko) | 2019-06-04 | 2022-02-10 | 다우 실리콘즈 코포레이션 | 실릴 수소화물과 실릴 에테르 및/또는 실라놀 사이의 열적으로 개시되는 산 촉매 반응 |
| JP7560488B2 (ja) | 2019-06-04 | 2024-10-02 | ダウ シリコーンズ コーポレーション | シリルヒドリドとシロキサンとの熱開始酸触媒反応 |
| KR20220016900A (ko) | 2019-06-04 | 2022-02-10 | 다우 실리콘즈 코포레이션 | Si-H와 Si-O-Si의 반응을 위한 열 트리거로서의 가교된 불완전 루이스 쌍 |
| EP3980428B1 (en) | 2019-06-04 | 2023-04-26 | Dow Silicones Corporation | Thermally initiated acid catalyzed reaction between silyl hydride and alpha-beta unsaturated esters |
| JP7560489B2 (ja) | 2019-06-04 | 2024-10-02 | ダウ シリコーンズ コーポレーション | Ｓｉ－Ｈとアルファ－ベータ不飽和エステルとの反応のための熱トリガとしての架橋型フラストレイテッドルイスペア |
| KR20220016903A (ko) * | 2019-06-04 | 2022-02-10 | 다우 실리콘즈 코포레이션 | Si-H와 에폭사이드의 반응을 위한 열 트리거로서의 가교된 불완전 루이스 쌍 |
| WO2020247334A1 (en) | 2019-06-04 | 2020-12-10 | Dow Silicones Corporation | Bridged frustrated lewis pairs as thermal trigger for reactions between si-h and si-or |
| WO2021146093A1 (en) * | 2020-01-14 | 2021-07-22 | University Of Vermont And State Agricultural College | Methods of preparing primary phosphine products using lewis acid catalysts |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4522932A (en) * | 1982-09-27 | 1985-06-11 | Exxon Research & Engineering Co. | Phosphine and phosphonium compounds and catalysts |
| CA2291616A1 (en) * | 1997-08-01 | 1999-02-11 | David J. Schwartz | Zwitterionic catalyst activator |
| US6395847B2 (en) * | 1999-11-19 | 2002-05-28 | Exxonmobil Chemical Patents Inc. | Supported organometallic catalysts and their use in olefin polymerization |
| GB0314220D0 (en) | 2003-06-19 | 2003-07-23 | Univ Durham | Bifunctional catalyst |
-
2007
- 2007-11-14 EP EP07873357A patent/EP2091957A4/en not_active Withdrawn
- 2007-11-14 KR KR1020097010781A patent/KR20090078835A/ko not_active Ceased
- 2007-11-14 MX MX2009005127A patent/MX2009005127A/es active IP Right Grant
- 2007-11-14 AU AU2007350983A patent/AU2007350983A1/en not_active Abandoned
- 2007-11-14 CA CA2669545A patent/CA2669545C/en not_active Expired - Fee Related
- 2007-11-14 SG SG2011083763A patent/SG176482A1/en unknown
- 2007-11-14 WO PCT/IB2007/004577 patent/WO2008125911A2/en not_active Ceased
- 2007-11-14 JP JP2009536823A patent/JP2010509393A/ja active Pending
- 2007-11-14 CN CN200780042370XA patent/CN102066390A/zh active Pending
- 2007-11-14 US US12/514,901 patent/US8299284B2/en not_active Expired - Fee Related
-
2012
- 2012-09-14 US US13/618,790 patent/US8642812B2/en not_active Expired - Fee Related
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP2010509393A5 (cg-RX-API-DMAC7.html) | ||
| Hosseini-Sarvari | TiO2 as a new and reusable catalyst for one-pot three-component syntheses of α-aminophosphonates in solvent-free conditions | |
| US8642812B2 (en) | Frustrated Lewis pair compositions | |
| CN101228103A (zh) | 作为过渡金属催化剂配体的稳定环(烷基)(氨基)卡宾 | |
| EP2445920A1 (en) | Phosphite containing catalysts for hydroformylation processes | |
| Yang et al. | Synthesis of novel chiral tridentate aminophenol ligands for enantioselective addition of diethylzinc to aldehydes | |
| CN103582623B (zh) | 醛化合物的制造方法 | |
| CN107286202B (zh) | 手性Ugi’s胺和其衍生物及光学异构体的合成方法和应用 | |
| CN103214446A (zh) | 一种色满酮衍生物的不对称合成方法 | |
| CN110156832A (zh) | 双缩醛基苯基膦、它们的制备方法及在偶联反应中的用途 | |
| JP4828773B2 (ja) | 不斉合成のためのリガンドとしてのキラルなモノホスファイト | |
| Signore et al. | Synthesis of N, N-disubstituted phosphoramidates via a Lewis acid-catalyzed phosphorimidate rearrangement | |
| WO2003066643A1 (fr) | Procede de production de phosphine tertiaire a groupe hydrocarbone volumineux lie | |
| CN118878543A (zh) | 一种轴手性环戊烯基并吲哚-萘基化合物及其制备方法与应用 | |
| CN113735867B (zh) | 一种手性吲哚并氧杂七元环化合物及其合成方法 | |
| US5654455A (en) | Tris-phosphite ligands and their use in transitioin metal catalyzed processes | |
| Gavrilov et al. | Pd-catalyzed asymmetric reactions using resorcinol-and hydroquinone-based P∗, P∗-bidentate diamidophosphites | |
| Gavrilov et al. | P∗, P∗-Bidentate diastereoisomeric bisdiamidophosphites based on N-benzyltartarimide and their applications in asymmetric catalytic processes | |
| JP2019011286A (ja) | ホスフィン化合物及びこれを配位子とするカップリング用触媒 | |
| GB2620096A (en) | Use of chiral bisphosphonate diamine compound | |
| Huelgas et al. | New ligands and structural insights into the catalytic asymmetric addition of organozinc reagents to ketones | |
| Gavrilov et al. | Phosphoramidites based on phenyl-substituted 1, 2-diols as ligands in palladium-catalyzed asymmetric allylations: the contribution of steric demand and chiral centers to the enantioselectivity | |
| JP4271454B2 (ja) | 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 | |
| Gavrilov et al. | Diastereomeric P, N-bidentate amidophosphites based on (S, S)-and (R, R)-hydrobenzoin as ligands in the Pd-catalyzed asymmetric allylation | |
| CN1300157C (zh) | 多齿膦化合物的制备方法 |