JP2005529961A5 - - Google Patents
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- Publication number
- JP2005529961A5 JP2005529961A5 JP2004514504A JP2004514504A JP2005529961A5 JP 2005529961 A5 JP2005529961 A5 JP 2005529961A5 JP 2004514504 A JP2004514504 A JP 2004514504A JP 2004514504 A JP2004514504 A JP 2004514504A JP 2005529961 A5 JP2005529961 A5 JP 2005529961A5
- Authority
- JP
- Japan
- Prior art keywords
- alkyl
- hydrogen
- methyl
- ethyl
- carbon atom
- 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
- 229910052739 hydrogen Inorganic materials 0.000 claims 27
- 239000001257 hydrogen Substances 0.000 claims 27
- 125000000217 alkyl group Chemical group 0.000 claims 23
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 15
- 150000002431 hydrogen Chemical class 0.000 claims 12
- 229910052799 carbon Inorganic materials 0.000 claims 11
- 125000004432 carbon atom Chemical group C* 0.000 claims 11
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 11
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 10
- 150000001875 compounds Chemical class 0.000 claims 8
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims 6
- 125000000753 cycloalkyl group Chemical group 0.000 claims 6
- TYBCSQFBSWACAA-UHFFFAOYSA-N Nonan-4-one Chemical compound CCCCCC(=O)CCC TYBCSQFBSWACAA-UHFFFAOYSA-N 0.000 claims 5
- 238000000034 method Methods 0.000 claims 5
- 125000004356 hydroxy functional group Chemical group O* 0.000 claims 4
- 230000029936 alkylation Effects 0.000 claims 2
- 238000005804 alkylation reaction Methods 0.000 claims 2
- 239000000796 flavoring agent Substances 0.000 claims 2
- 235000019634 flavors Nutrition 0.000 claims 2
- 239000003205 fragrance Substances 0.000 claims 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 2
- GATPISAXWKJNLE-UHFFFAOYSA-N 1,3-dimethyl-5-propan-2-ylbicyclo[3.2.1]oct-3-en-2-one Chemical compound C1C2(C)CCC1(C(C)C)C=C(C)C2=O GATPISAXWKJNLE-UHFFFAOYSA-N 0.000 claims 1
- JZCFBLXJYIBMPQ-UHFFFAOYSA-N 1,3-dimethyl-5-propan-2-ylbicyclo[3.2.1]octan-2-one Chemical compound C1C2(C)CCC1(C(C)C)CC(C)C2=O JZCFBLXJYIBMPQ-UHFFFAOYSA-N 0.000 claims 1
- IZEQHCDKTWURGG-UHFFFAOYSA-N 3,3,5-trimethyl-1-propan-2-yltricyclo[3.2.1.02,7]octan-6-one Chemical compound C1C(C)(C)C2C3(C(C)C)C2C(=O)C1(C)C3 IZEQHCDKTWURGG-UHFFFAOYSA-N 0.000 claims 1
- GEFVOCKUJOIGLW-UHFFFAOYSA-N 3,7,7-trimethyl-5-propan-2-ylbicyclo[3.2.1]oct-3-en-2-one Chemical compound C1C2C(=O)C(C)=CC1(C(C)C)CC2(C)C GEFVOCKUJOIGLW-UHFFFAOYSA-N 0.000 claims 1
- DCTPZCNXWQSVRY-UHFFFAOYSA-N 3-methyl-5,7-di(propan-2-yl)bicyclo[3.2.1]oct-3-en-2-one Chemical compound C1C2C(C(C)C)CC1(C(C)C)C=C(C)C2=O DCTPZCNXWQSVRY-UHFFFAOYSA-N 0.000 claims 1
- WWRVNVDNYMCAIC-UHFFFAOYSA-N 3-methyl-5-propan-2-ylbicyclo[3.2.1]oct-3-en-2-one Chemical compound C1C2CCC1(C(C)C)C=C(C)C2=O WWRVNVDNYMCAIC-UHFFFAOYSA-N 0.000 claims 1
- MJKCHFCQEWZMHD-UHFFFAOYSA-N 5-butan-2-yl-1,3-dimethylbicyclo[3.2.1]oct-3-en-2-one Chemical compound C1C2(C)CCC1(C(C)CC)C=C(C)C2=O MJKCHFCQEWZMHD-UHFFFAOYSA-N 0.000 claims 1
- DLMOCLNSSYFXAF-UHFFFAOYSA-N 5-tert-butyl-1,3-dimethylbicyclo[3.2.1]oct-3-en-2-one Chemical compound O=C1C(C)=CC2(C(C)(C)C)CCC1(C)C2 DLMOCLNSSYFXAF-UHFFFAOYSA-N 0.000 claims 1
- 125000004965 chloroalkyl group Chemical group 0.000 claims 1
- UAIZDWNSWGTKFZ-UHFFFAOYSA-L ethylaluminum(2+);dichloride Chemical compound CC[Al](Cl)Cl UAIZDWNSWGTKFZ-UHFFFAOYSA-L 0.000 claims 1
- 230000006698 induction Effects 0.000 claims 1
- YSTQWZZQKCCBAY-UHFFFAOYSA-L methylaluminum(2+);dichloride Chemical compound C[Al](Cl)Cl YSTQWZZQKCCBAY-UHFFFAOYSA-L 0.000 claims 1
- IXUOEGRSQCCEHB-UHFFFAOYSA-N nonan-4-ol Chemical compound CCCCCC(O)CCC IXUOEGRSQCCEHB-UHFFFAOYSA-N 0.000 claims 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims 1
- 239000000758 substrate Substances 0.000 claims 1
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GBGB0214344.4A GB0214344D0 (en) | 2002-06-21 | 2002-06-21 | New odorant Compounds |
| PCT/CH2003/000401 WO2004000776A1 (en) | 2002-06-21 | 2003-06-20 | Alcohols and ketones of bi- and tricyclic compounds and odorant compositions |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2005529961A JP2005529961A (ja) | 2005-10-06 |
| JP2005529961A5 true JP2005529961A5 (https=) | 2006-08-03 |
Family
ID=9939037
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2004514504A Pending JP2005529961A (ja) | 2002-06-21 | 2003-06-20 | 二環式および三環式化合物のアルコール類およびケトン類ならびに臭気組成物 |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US7691802B2 (https=) |
| EP (1) | EP1515938A1 (https=) |
| JP (1) | JP2005529961A (https=) |
| CN (1) | CN1301953C (https=) |
| AU (1) | AU2003240348A1 (https=) |
| GB (1) | GB0214344D0 (https=) |
| MX (1) | MXPA04012277A (https=) |
| WO (1) | WO2004000776A1 (https=) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| PL1712547T3 (pl) | 2004-02-05 | 2012-04-30 | Kyorin Seiyaku Kk | Pochodna bicykloestrowa |
| GB0424643D0 (en) * | 2004-11-09 | 2004-12-08 | Givaudan Sa | Organic compounds |
| GB0916363D0 (en) * | 2009-09-18 | 2009-10-28 | Givaudan Sa | Organic compounds |
| EP2580309B1 (en) * | 2010-06-08 | 2014-07-16 | Firmenich SA | Bicyclo-ketones as perfuming ingredients |
| EP2687586B1 (de) | 2012-07-17 | 2016-11-23 | Symrise AG | Verwendung definierter Cyclohexenone als Mittel zum überadditiven Verstärken eines Geruchseindrucks sowie Riech- und/oder Geschmacksstoffkomposition |
| AU2024281198A1 (en) | 2023-05-31 | 2025-11-27 | Chemosensoryx Biosciences S.A. | Lightening compositions and use of compounds as depigmenting agents |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3679750A (en) * | 1968-06-10 | 1972-07-25 | Int Flavors & Fragrances Inc | Hexahydro-1,4,9,9-tetramethyl-4,7-methano-azulenones |
| CH589577A5 (https=) | 1974-08-23 | 1977-07-15 | Firmenich & Cie | |
| US4947002A (en) * | 1987-11-12 | 1990-08-07 | Givaudan Corporation | Novel tricyclic ketones and fragrance compositions containing same |
| CN1045082C (zh) * | 1996-01-31 | 1999-09-15 | 南京林业大学 | 一种花香型香料及其合成方法 |
| DE19835323A1 (de) * | 1998-08-05 | 2000-02-10 | Aventis Res & Tech Gmbh & Co | Verfahren zur katalytischen Oxidation von 1,5-Dialkylbicyclo(3.2.1)octan-8-ol zu 1,5-Dialkylbicyclo(3.2.1)octan-8-on |
-
2002
- 2002-06-21 GB GBGB0214344.4A patent/GB0214344D0/en not_active Ceased
-
2003
- 2003-06-20 MX MXPA04012277A patent/MXPA04012277A/es active IP Right Grant
- 2003-06-20 WO PCT/CH2003/000401 patent/WO2004000776A1/en not_active Ceased
- 2003-06-20 AU AU2003240348A patent/AU2003240348A1/en not_active Abandoned
- 2003-06-20 JP JP2004514504A patent/JP2005529961A/ja active Pending
- 2003-06-20 EP EP03729764A patent/EP1515938A1/en not_active Ceased
- 2003-06-20 CN CNB038145596A patent/CN1301953C/zh not_active Expired - Fee Related
- 2003-06-20 US US10/518,565 patent/US7691802B2/en not_active Expired - Fee Related
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