JPWO2024075678A5 - - Google Patents
Download PDFInfo
- Publication number
- JPWO2024075678A5 JPWO2024075678A5 JP2024555789A JP2024555789A JPWO2024075678A5 JP WO2024075678 A5 JPWO2024075678 A5 JP WO2024075678A5 JP 2024555789 A JP2024555789 A JP 2024555789A JP 2024555789 A JP2024555789 A JP 2024555789A JP WO2024075678 A5 JPWO2024075678 A5 JP WO2024075678A5
- Authority
- JP
- Japan
- Prior art keywords
- bio
- derived
- ring
- linear
- primary alcohol
- 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
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2022162316 | 2022-10-07 | ||
| JP2022162316 | 2022-10-07 | ||
| PCT/JP2023/035861 WO2024075678A1 (ja) | 2022-10-07 | 2023-10-02 | バイオ由来分岐アルキルグリセリルエーテルの製造方法及び該方法により製造されるバイオ由来分岐アルキルグリセリルエーテル |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JPWO2024075678A1 JPWO2024075678A1 (https=) | 2024-04-11 |
| JPWO2024075678A5 true JPWO2024075678A5 (https=) | 2025-01-09 |
| JP7702048B2 JP7702048B2 (ja) | 2025-07-02 |
Family
ID=90608087
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2024555789A Active JP7702048B2 (ja) | 2022-10-07 | 2023-10-02 | バイオ由来分岐アルキルグリセリルエーテルの製造方法及び該方法により製造されるバイオ由来分岐アルキルグリセリルエーテル |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US12528755B2 (https=) |
| EP (1) | EP4509491A4 (https=) |
| JP (1) | JP7702048B2 (https=) |
| KR (1) | KR102891747B1 (https=) |
| CN (1) | CN119343328B (https=) |
| WO (1) | WO2024075678A1 (https=) |
Family Cites Families (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS542249B2 (https=) | 1974-12-26 | 1979-02-05 | ||
| JPS5212109A (en) * | 1975-07-17 | 1977-01-29 | New Japan Chem Co Ltd | Process for preparation of alkylglycerylether |
| JPS5639033A (en) * | 1979-09-04 | 1981-04-14 | Kao Corp | Alpha-mono(methyl-branched alkyl glyceryl ether and skin cosmetic containing the same |
| JP3543447B2 (ja) | 1995-11-07 | 2004-07-14 | 三菱化学株式会社 | 二量化アルデヒドの製造方法 |
| FR2734158B1 (fr) | 1995-05-17 | 1997-06-27 | Roche Posay Lab Pharma | Association d'un compose a activite anti-microbienne et d'un monoalkylether de glycerol |
| JP3544134B2 (ja) | 1999-01-25 | 2004-07-21 | 花王株式会社 | グリセリルエーテルの製造法 |
| JP2002163692A (ja) | 2000-11-29 | 2002-06-07 | Nippon Signal Co Ltd:The | 非接触式icカードリーダライタ |
| JP2007084464A (ja) | 2005-09-21 | 2007-04-05 | Adeka Corp | 化粧料組成物 |
| DE102012105876A1 (de) | 2012-07-02 | 2014-01-02 | Oxea Gmbh | Verfahren zur Herstellung von Terephthalsäure und ihren Derivaten |
| CN104402682A (zh) | 2014-11-10 | 2015-03-11 | 平湖优康药物研发有限公司 | 一种新型化妆品抗菌剂辛氧基甘油的合成工艺 |
| JP6598671B2 (ja) | 2015-12-24 | 2019-10-30 | 花王株式会社 | フラックス用洗浄剤組成物 |
| JP7362640B2 (ja) | 2018-09-25 | 2023-10-17 | 株式会社Adeka | グリセリルエーテル含有組成物の製造方法およびグリセリルエーテル含有組成物 |
| WO2020116534A1 (ja) | 2018-12-05 | 2020-06-11 | 花王株式会社 | フラックス残渣の洗浄 |
| JP7301707B2 (ja) | 2019-10-03 | 2023-07-03 | 株式会社ナリス化粧品 | ふきとり用化粧料 |
| CA3183245A1 (en) * | 2020-05-22 | 2021-11-25 | Inolex Investment Corporation | Biobased alkyl glyceryl ethers and methods of making and using the same |
| JP2022163692A (ja) * | 2021-04-14 | 2022-10-26 | 株式会社Adeka | アルキルグリセリルエーテルの製造方法、アルキルグリセリルエーテル及び該アルキルグリセリルエーテルを含有する化粧料組成物又は洗浄剤組成物 |
-
2023
- 2023-10-02 CN CN202380045723.0A patent/CN119343328B/zh active Active
- 2023-10-02 US US18/871,701 patent/US12528755B2/en active Active
- 2023-10-02 WO PCT/JP2023/035861 patent/WO2024075678A1/ja not_active Ceased
- 2023-10-02 KR KR1020247038202A patent/KR102891747B1/ko active Active
- 2023-10-02 JP JP2024555789A patent/JP7702048B2/ja active Active
- 2023-10-02 EP EP23874805.7A patent/EP4509491A4/en active Pending
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| Lee et al. | Lasonolide A: structural revision and synthesis of the unnatural (−)-enantiomer | |
| Gao et al. | Recent progress in chemical syntheses of sphingosines and phytosphingosines | |
| Evans et al. | Diastereoselective construction of syn-1, 3-dioxanes via a Bismuth-mediated two-component hemiacetal/oxa-conjugate addition reaction | |
| Čusak | Temporary Silicon‐Tethered Ring‐Closing Metathesis: Recent Advances in Methodology Development and Natural Product Synthesis | |
| Gowda et al. | Synthesis of β-methyl-α-methylene-γ-butyrolactone from biorenewable itaconic acid | |
| Li et al. | Synthesis of 3‐Oxaterpenoids and Its Application in the Total Synthesis of (±)‐Moluccanic Acid Methyl Ester | |
| Chtourou et al. | Solvent free synthesis of 1, 3-diaryl-2-propenones catalyzed by commercial acid-clays under ultrasound irradiation | |
| CN102030612B (zh) | 利用含醇废液制备正丁醇的方法 | |
| Mushtaq et al. | Mukaiyama aldol reaction: an effective asymmetric approach to access chiral natural products and their derivatives/analogues | |
| JPWO2024075678A5 (https=) | ||
| Harris et al. | Enantioselective synthesis of 5-substituted α, β-unsaturated δ-lactones: application to the synthesis of styryllactones | |
| Sabitha et al. | Stereoselective total synthesis of (+)-anamarine via cross-metathesis protocol | |
| Ghosal et al. | A chiron approach to the total synthesis of cytotoxic (+)-muricatacin and (+)-5-epi-muricatacin from d-ribose | |
| Rainier | Synthesis of substituted tetrahydrofurans | |
| Butt et al. | A rearrangement-based approach to secondary difluorophosphonates | |
| Rana et al. | Synthesis of macrocyclic lactones and dilactones using olive oil | |
| Nonaka et al. | Improved synthesis of the polyhydroxylated central part of phoslactomycin B | |
| Katoh | Total synthesis of diterpenoid pyrones, nalanthalide, sesquicillin, candelalides A–C, and subglutinols A, B | |
| Sabitha et al. | First stereoselective total synthesis of seimatopolide A | |
| Ramesh | Protecting-Group-Free Total Synthesis of 8-Methoxygoniodiol | |
| Sathyamoorthi et al. | Ring-Opening of Aziridines Using Tethered Hemiketals | |
| Yang et al. | Stereoselective synthesis of (−)-centrolobine | |
| Kaur | Oxetane synthesis | |
| Halperin et al. | Lithium aldol reactions of α-chloroaldehydes provide versatile building blocks for natural product synthesis | |
| JPH03130276A (ja) | α―アルキルラクトンの製法 |