JP2016506393A5 - - Google Patents
Download PDFInfo
- Publication number
- JP2016506393A5 JP2016506393A5 JP2015547085A JP2015547085A JP2016506393A5 JP 2016506393 A5 JP2016506393 A5 JP 2016506393A5 JP 2015547085 A JP2015547085 A JP 2015547085A JP 2015547085 A JP2015547085 A JP 2015547085A JP 2016506393 A5 JP2016506393 A5 JP 2016506393A5
- Authority
- JP
- Japan
- Prior art keywords
- group
- alkyl group
- alkyl
- formula
- complex
- 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
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 description 11
- 125000003118 aryl group Chemical group 0.000 description 4
- 125000005843 halogen group Chemical group 0.000 description 4
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 4
- 229910052741 iridium Inorganic materials 0.000 description 4
- 125000002723 alicyclic group Chemical group 0.000 description 3
- 125000003545 alkoxy group Chemical group 0.000 description 3
- 125000000217 alkyl group Chemical group 0.000 description 3
- GKOZUEZYRPOHIO-UHFFFAOYSA-N iridium atom Chemical compound [Ir] GKOZUEZYRPOHIO-UHFFFAOYSA-N 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 229910020366 ClO 4 Inorganic materials 0.000 description 2
- 229910018286 SbF 6 Inorganic materials 0.000 description 2
- HFKJQIJFRMRSKM-UHFFFAOYSA-N [3,5-bis(trifluoromethyl)phenoxy]boronic acid Chemical compound OB(O)OC1=CC(C(F)(F)F)=CC(C(F)(F)F)=C1 HFKJQIJFRMRSKM-UHFFFAOYSA-N 0.000 description 2
- 150000001450 anions Chemical class 0.000 description 2
- 229940063013 borate ion Drugs 0.000 description 2
- 150000004820 halides Chemical class 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 239000013110 organic ligand Substances 0.000 description 2
- -1 perfluorinated sulfonic acid Ions Chemical class 0.000 description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
- 125000006713 (C5-C10) cycloalkyl group Chemical group 0.000 description 1
- 125000006705 (C5-C7) cycloalkyl group Chemical group 0.000 description 1
- 125000001637 1-naphthyl group Chemical group [H]C1=C([H])C([H])=C2C(*)=C([H])C([H])=C([H])C2=C1[H] 0.000 description 1
- 125000002941 2-furyl group Chemical group O1C([*])=C([H])C([H])=C1[H] 0.000 description 1
- 125000001622 2-naphthyl group Chemical group [H]C1=C([H])C([H])=C2C([H])=C(*)C([H])=C([H])C2=C1[H] 0.000 description 1
- 125000005073 adamantyl group Chemical group C12(CC3CC(CC(C1)C3)C2)* 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 125000004429 atom Chemical group 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
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 239000011203 carbon fibre reinforced carbon Substances 0.000 description 1
- 150000001993 dienes Chemical class 0.000 description 1
- 150000002503 iridium Chemical class 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
- 125000003261 o-tolyl group Chemical group [H]C1=C([H])C(*)=C(C([H])=C1[H])C([H])([H])[H] 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
- 125000004437 phosphorous atom Chemical group 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP12197812 | 2012-12-18 | ||
| EP12197812.6 | 2012-12-18 | ||
| PCT/EP2013/077233 WO2014096098A1 (en) | 2012-12-18 | 2013-12-18 | (6r,10r)-6,10,14-trimetylpentadecan-2-one prepared from 6,10,14-trimetylpentadeca-5,9,13-trien-2-one or 6,10,14-trimetylpentadeca-5,9-dien-2-one |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2016506393A JP2016506393A (ja) | 2016-03-03 |
| JP2016506393A5 true JP2016506393A5 (enExample) | 2019-02-28 |
| JP6582324B2 JP6582324B2 (ja) | 2019-10-02 |
Family
ID=47458691
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2015547085A Active JP6582324B2 (ja) | 2012-12-18 | 2013-12-18 | ６，１０，１４−トリメチルペンタデカ−５，９，１３−トリエン−２−オンまたは６，１０，１４−トリメチルペンタデカ−５，９−ジエン−２−オンから調製した（６ｒ，１０ｒ）−６，１０，１４−トリメチルペンタデカン−２−オン |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US9611200B2 (enExample) |
| EP (1) | EP2935185B1 (enExample) |
| JP (1) | JP6582324B2 (enExample) |
| CN (1) | CN104854071B (enExample) |
| BR (1) | BR112015014423B1 (enExample) |
| EA (1) | EA033302B9 (enExample) |
| MY (1) | MY173272A (enExample) |
| WO (1) | WO2014096098A1 (enExample) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US9452961B2 (en) * | 2012-12-18 | 2016-09-27 | Dsm Ip Assets B.V. | (6R,10R)-6,10,14-trimetylpentadecan-2-one prepared from 6,10-dimetylundec-5-en-2-one or 6,10-dimetylundeca-5,9-dien-2-one |
| JP6390048B2 (ja) * | 2012-12-18 | 2018-09-19 | ディーエスエム アイピー アセッツ ビー．ブイ．Ｄｓｍ Ｉｐ Ａｓｓｅｔｓ Ｂ．Ｖ． | 組み合わされた不斉水素化によって特定の生成物を定量的に得るためのｅ／ｚ異性体の混合物の使用 |
| JP6406676B2 (ja) * | 2012-12-18 | 2018-10-17 | ディーエスエム アイピー アセッツ ビー．ブイ．Ｄｓｍ Ｉｐ Ａｓｓｅｔｓ Ｂ．Ｖ． | 不斉水素化および異性化を組み合わせることによって特定の生成物を定量的に得るためのｅ／ｚ異性体の混合物の使用 |
| WO2017098050A1 (en) * | 2015-12-11 | 2017-06-15 | Dsm Ip Assets B.V. | Process for the manufacture of 6,10,14-trimethylpentadecan-2-one, isophytol and alpha-tocopherol |
| EP4034528A1 (en) | 2019-09-25 | 2022-08-03 | Bayer Aktiengesellschaft | Process comprising the use of new iridium catalysts for enantioselective hydrogenation of 4-substituted 1,2-dihydroquinolines |
Family Cites Families (22)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5132511A (en) * | 1974-09-10 | 1976-03-19 | Kuraray Co | Ritsutaikiseisareta geraniruaseton no seizohoho |
| US4028385A (en) | 1974-09-02 | 1977-06-07 | Kuraray Co., Ltd. | Process for preparing stereospecific farnesylacetic acid and ester thereof |
| JPS6036479A (ja) * | 1983-08-08 | 1985-02-25 | Kotobuki Seiyaku Kk | １，３−ジオキサン誘導体、本化合物を有効成分とする抗潰瘍剤及びその製造方法 |
| US5028385A (en) | 1989-04-10 | 1991-07-02 | Baldi Alfonso L | Treatment of metals for coating or activation |
| US5073659A (en) * | 1989-08-22 | 1991-12-17 | Eisai Co., Ltd. | Process for the preparation of terpenes |
| DK0565975T3 (da) * | 1992-04-16 | 1996-10-14 | Hoffmann La Roche | Fremgangsmåde til fremstilling af isoprenderivater |
| US5349071A (en) * | 1992-11-25 | 1994-09-20 | Loyola University Of Chicago | Process for preparing tertiary alkynols |
| US5955636A (en) * | 1996-07-05 | 1999-09-21 | Kuraray Co., Ltd. | Process for producing 6-methyl-3-hepten-2-one and 6-methyl-2-heptanone analogues, and process for producing phyton or isophytol |
| EP0970953B1 (en) | 1998-07-10 | 2004-09-29 | DSM IP Assets B.V. | Manufacture of d,1-alpha-tocopherol |
| DE19840747A1 (de) | 1998-09-07 | 2000-03-09 | Basf Ag | Kontinuierliches Verfahren zur Herstellung von ungesättigten Ketonen |
| CN1242968C (zh) | 2001-09-28 | 2006-02-22 | Dsmip资产有限公司 | 乙炔化方法 |
| JP4780959B2 (ja) | 2002-08-16 | 2011-09-28 | ディーエスエム アイピー アセッツ ビー．ブイ． | エチニル化法 |
| EP1778661B1 (en) | 2004-06-11 | 2014-01-22 | DSM IP Assets B.V. | Process for the manufacture of chroman derivatives, especially alpha-tocopherol and alkanoates thereof |
| JP5090926B2 (ja) * | 2004-12-22 | 2012-12-05 | ディーエスエム アイピー アセッツ ビー．ブイ． | キラルイリジウム錯体を使用するアルケンの不斉水素化 |
| EP2522647B1 (en) | 2011-05-10 | 2014-04-30 | DSM IP Assets B.V. | Process of separating chiral isomers of chroman compounds and their derivatives and precursors |
| EP2535323A1 (en) * | 2011-06-14 | 2012-12-19 | DSM IP Assets B.V. | Hydrogenation of ketones having at least a carbon-carbon double bond in the gamma-,delta-position |
| JP6442782B2 (ja) * | 2012-12-18 | 2018-12-26 | ディーエスエム アイピー アセッツ ビー．ブイ．Ｄｓｍ Ｉｐ Ａｓｓｅｔｓ Ｂ．Ｖ． | 不飽和化合物のためのシス／トランス異性化触媒としてのポリチオール |
| JP6390048B2 (ja) * | 2012-12-18 | 2018-09-19 | ディーエスエム アイピー アセッツ ビー．ブイ．Ｄｓｍ Ｉｐ Ａｓｓｅｔｓ Ｂ．Ｖ． | 組み合わされた不斉水素化によって特定の生成物を定量的に得るためのｅ／ｚ異性体の混合物の使用 |
| CN110563566A (zh) * | 2012-12-18 | 2019-12-13 | 帝斯曼知识产权资产管理有限公司 | 一氧化氮作为不饱和化合物的顺式/反式异构化催化剂 |
| US9452961B2 (en) * | 2012-12-18 | 2016-09-27 | Dsm Ip Assets B.V. | (6R,10R)-6,10,14-trimetylpentadecan-2-one prepared from 6,10-dimetylundec-5-en-2-one or 6,10-dimetylundeca-5,9-dien-2-one |
| CN104936938B (zh) * | 2012-12-18 | 2017-05-31 | 帝斯曼知识产权资产管理有限公司 | 使用添加剂不对称氢化不饱和酮的有效方法 |
| JP6406676B2 (ja) * | 2012-12-18 | 2018-10-17 | ディーエスエム アイピー アセッツ ビー．ブイ．Ｄｓｍ Ｉｐ Ａｓｓｅｔｓ Ｂ．Ｖ． | 不斉水素化および異性化を組み合わせることによって特定の生成物を定量的に得るためのｅ／ｚ異性体の混合物の使用 |
-
2013
- 2013-12-18 EA EA201500665A patent/EA033302B9/ru not_active IP Right Cessation
- 2013-12-18 BR BR112015014423-3A patent/BR112015014423B1/pt active IP Right Grant
- 2013-12-18 JP JP2015547085A patent/JP6582324B2/ja active Active
- 2013-12-18 MY MYPI2015701971A patent/MY173272A/en unknown
- 2013-12-18 WO PCT/EP2013/077233 patent/WO2014096098A1/en not_active Ceased
- 2013-12-18 US US14/652,297 patent/US9611200B2/en active Active
- 2013-12-18 EP EP13814521.4A patent/EP2935185B1/en active Active
- 2013-12-18 CN CN201380065784.XA patent/CN104854071B/zh active Active
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP2016506393A5 (enExample) | ||
| Bulfield et al. | Halogen bonding in organic synthesis and organocatalysis | |
| JP2015537020A5 (enExample) | ||
| Adhikary et al. | Synthesis and Characterization of Two Discrete Ln10 Nanoscopic Ladder‐Type Cages: Magnetic Studies Reveal a Significant Cryogenic Magnetocaloric Effect and Slow Magnetic Relaxation | |
| JP2014524888A5 (enExample) | ||
| Zareba et al. | Extending the family of tetrahedral tectons: phenyl embraces in supramolecular polymers of tetraphenylmethane-based tetraphosphonic acid templated by organic bases | |
| JP2013147496A5 (ja) | 有機金属錯体 | |
| JP2010511017A5 (enExample) | ||
| JP2010501572A5 (enExample) | ||
| Yue et al. | Supramolecular engineering of a 2D Kagomé lattice: Synthesis, structures, and magnetic properties | |
| JP2013010749A5 (ja) | カルバゾール化合物 | |
| JP2013102146A5 (ja) | 化合物 | |
| JP2015537054A5 (enExample) | ||
| JP2014508811A5 (enExample) | ||
| JP2013126982A5 (ja) | 有機金属錯体及び発光材料 | |
| JP2014515351A5 (enExample) | ||
| JP2012248871A5 (ja) | 発光素子および発光装置 | |
| Zhang et al. | Iridium-catalyzed selective B (4)–H acylmethylation of o-carboranes with sulfoxonium ylides | |
| JP2013147490A5 (ja) | イリジウム錯体 | |
| JP2014534180A5 (enExample) | ||
| CN109311812A (zh) | 作为c-MET抑制剂的吡啶酮类化合物 | |
| JP2014047406A5 (enExample) | ||
| JP2014097964A5 (enExample) | ||
| Zhao et al. | Synthesis and Characterization of Copper (I) Halide Complexes with N‐(2, 6‐Diisopropylphenyl)‐N′‐benzoylthiourea: Monomeric, Dimeric, and Cage Structures | |
| ES2213523T3 (es) | Compuestos de aminofosfonio. |