JP2004315396A5 - - Google Patents
Download PDFInfo
- Publication number
- JP2004315396A5 JP2004315396A5 JP2003109523A JP2003109523A JP2004315396A5 JP 2004315396 A5 JP2004315396 A5 JP 2004315396A5 JP 2003109523 A JP2003109523 A JP 2003109523A JP 2003109523 A JP2003109523 A JP 2003109523A JP 2004315396 A5 JP2004315396 A5 JP 2004315396A5
- Authority
- JP
- Japan
- Prior art keywords
- group
- carbon atoms
- alkyl group
- optically active
- embedded image
- 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
- 125000004432 carbon atom Chemical group C* 0.000 description 33
- 125000000217 alkyl group Chemical group 0.000 description 17
- 125000003545 alkoxy group Chemical group 0.000 description 7
- 238000004519 manufacturing process Methods 0.000 description 7
- 125000003277 amino group Chemical group 0.000 description 5
- 125000004435 hydrogen atom Chemical class [H]* 0.000 description 5
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 5
- -1 phosphine compound Chemical class 0.000 description 5
- 125000002252 acyl group Chemical group 0.000 description 4
- 125000004093 cyano group Chemical group *C#N 0.000 description 4
- 239000010948 rhodium Substances 0.000 description 4
- XYFCBTPGUUZFHI-UHFFFAOYSA-N Phosphine Natural products P XYFCBTPGUUZFHI-UHFFFAOYSA-N 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical group [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- 125000004453 alkoxycarbonyl group Chemical group 0.000 description 3
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 description 3
- 229910000073 phosphorus hydride Inorganic materials 0.000 description 3
- 125000004414 alkyl thio group Chemical group 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 description 2
- 125000005843 halogen group Chemical group 0.000 description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
- 229910052703 rhodium Inorganic materials 0.000 description 2
- MHOVAHRLVXNVSD-UHFFFAOYSA-N rhodium atom Chemical compound [Rh] MHOVAHRLVXNVSD-UHFFFAOYSA-N 0.000 description 2
- 150000003284 rhodium compounds Chemical class 0.000 description 2
- 0 CN(C)C(**)=C(*)C=O Chemical compound CN(C)C(**)=C(*)C=O 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 229910020366 ClO 4 Inorganic materials 0.000 description 1
- 229910018286 SbF 6 Inorganic materials 0.000 description 1
- CUJRVFIICFDLGR-UHFFFAOYSA-N acetylacetonate Chemical compound CC(=O)[CH-]C(C)=O CUJRVFIICFDLGR-UHFFFAOYSA-N 0.000 description 1
- 125000004423 acyloxy group Chemical group 0.000 description 1
- 125000003342 alkenyl group Chemical group 0.000 description 1
- 125000000304 alkynyl group Chemical group 0.000 description 1
- 150000008064 anhydrides Chemical class 0.000 description 1
- 150000001543 aryl boronic acids Chemical class 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 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
- MUALRAIOVNYAIW-UHFFFAOYSA-N binap Chemical compound C1=CC=CC=C1P(C=1C(=C2C=CC=CC2=CC=1)C=1C2=CC=CC=C2C=CC=1P(C=1C=CC=CC=1)C=1C=CC=CC=1)C1=CC=CC=C1 MUALRAIOVNYAIW-UHFFFAOYSA-N 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 125000001309 chloro group Chemical group Cl* 0.000 description 1
- 125000002933 cyclohexyloxy group Chemical group C1(CCCCC1)O* 0.000 description 1
- AFQSOHSPTULSFS-FGSKAQBVSA-N ethene;(z)-4-hydroxypent-3-en-2-one;rhodium Chemical compound [Rh].C=C.C=C.C\C(O)=C\C(C)=O AFQSOHSPTULSFS-FGSKAQBVSA-N 0.000 description 1
- YFXCNIVBAVFOBX-UHFFFAOYSA-N ethenylboronic acid Chemical compound OB(O)C=C YFXCNIVBAVFOBX-UHFFFAOYSA-N 0.000 description 1
- 125000005678 ethenylene group Chemical group [H]C([*:1])=C([H])[*:2] 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 125000001153 fluoro group Chemical group F* 0.000 description 1
- 125000003709 fluoroalkyl group Chemical group 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 125000004573 morpholin-4-yl group Chemical group N1(CCOCC1)* 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
- 125000006678 phenoxycarbonyl group Chemical group 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2003109523A JP4351859B2 (ja) | 2003-04-14 | 2003-04-14 | 光学活性β−アリ−ル化合物の製造法 |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2003109523A JP4351859B2 (ja) | 2003-04-14 | 2003-04-14 | 光学活性β−アリ−ル化合物の製造法 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2004315396A JP2004315396A (ja) | 2004-11-11 |
| JP2004315396A5 true JP2004315396A5 (enExample) | 2006-06-08 |
| JP4351859B2 JP4351859B2 (ja) | 2009-10-28 |
Family
ID=33470655
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2003109523A Expired - Fee Related JP4351859B2 (ja) | 2003-04-14 | 2003-04-14 | 光学活性β−アリ−ル化合物の製造法 |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP4351859B2 (enExample) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR100890696B1 (ko) * | 2005-01-28 | 2009-03-26 | 아이알엠 엘엘씨 | 아릴 피롤리돈의 합성 |
| EP1854802A4 (en) | 2005-02-17 | 2008-06-25 | Japan Science & Tech Agency | A CATALYST FOR ASYMMETRIC SYNTHESIS, LIGAND FOR THE USE THEREOF, AND METHOD FOR PRODUCING OPTICALLY ACTIVE CONNECTION BY AN ASYMMETRIC SYNTHESIS ACTION USING THE SAME |
| JPWO2008010455A1 (ja) * | 2006-07-19 | 2009-12-17 | 国立大学法人 北海道大学 | β‐ジアリール電子吸引性基置換化合物の製造方法 |
| EP3166923B1 (en) * | 2014-07-10 | 2023-03-15 | SpecGx LLC | Process for preparing substituted phenylalkanes |
-
2003
- 2003-04-14 JP JP2003109523A patent/JP4351859B2/ja not_active Expired - Fee Related
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP2003506426A5 (enExample) | ||
| CY1110986T1 (el) | Αζολια ως αναστολεις της αποκαρβοξυλασης μηλονυλο-συνενζυμου α χρησιμα ως μεταβολικοι διαμορφωτες | |
| JP2005536503A5 (enExample) | ||
| JP2007509926A5 (enExample) | ||
| JP2001515084A5 (enExample) | ||
| JP2008544074A5 (enExample) | ||
| JP2004505965A5 (enExample) | ||
| JP2004529953A5 (enExample) | ||
| JP2001233915A5 (enExample) | ||
| JP2004315396A5 (enExample) | ||
| JP2004531479A5 (enExample) | ||
| JP2004051592A5 (enExample) | ||
| JP4134272B2 (ja) | 光学活性アミノホスフィニルブタン酸類の製造方法 | |
| JP2008542386A5 (enExample) | ||
| JP2006510659A5 (enExample) | ||
| JP2004502696A5 (enExample) | ||
| JP2010510217A5 (enExample) | ||
| JPH11228560A5 (enExample) | ||
| JP2002220391A5 (enExample) | ||
| JP2004315457A5 (enExample) | ||
| JP2004525111A5 (enExample) | ||
| JP2005525390A5 (enExample) | ||
| JP2000109457A5 (enExample) | ||
| JP2004018389A5 (enExample) | ||
| JPWO2022215652A5 (enExample) |