JPWO2024075678A5 - - Google Patents

Download PDF

Info

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
Application number
JP2024555789A
Other languages
English (en)
Japanese (ja)
Other versions
JPWO2024075678A1 (https=
JP7702048B2 (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/JP2023/035861 external-priority patent/WO2024075678A1/ja
Publication of JPWO2024075678A1 publication Critical patent/JPWO2024075678A1/ja
Publication of JPWO2024075678A5 publication Critical patent/JPWO2024075678A5/ja
Application granted granted Critical
Publication of JP7702048B2 publication Critical patent/JP7702048B2/ja
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

JP2024555789A 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 Active JP7702048B2 (ja)

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)

* Cited by examiner, † Cited by third party
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
CN113165027B (zh) 2018-12-05 2023-07-07 花王株式会社 助焊剂残渣的清洗
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
BR112022021837A2 (pt) * 2020-05-22 2022-12-13 Inolex Investment Corp Alquil gliceril éteres de base biológica e métodos de preparação e uso dos mesmos
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

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
Chtourou et al. Solvent free synthesis of 1, 3-diaryl-2-propenones catalyzed by commercial acid-clays under ultrasound irradiation
Latif et al. Stereoselective Construction of 2, 6-cis-Disubstituted Tetrahydropyrans via Intramolecular Amide Enolate Alkylation: Total Synthesis of (−)-Centrolobine
CN102030612B (zh) 利用含醇废液制备正丁醇的方法
JPWO2024075678A5 (https=)
Harris et al. Enantioselective synthesis of 5-substituted α, β-unsaturated δ-lactones: application to the synthesis of styryllactones
Mu et al. Total synthesis of D-lyxo-phytosphingosine and formal synthesis of pachastrissamine via a chiral 1, 3-oxazine
Sabitha et al. Stereoselective total synthesis of (+)-anamarine via cross-metathesis protocol
Rainier Synthesis of substituted tetrahydrofurans
Butt et al. A rearrangement-based approach to secondary difluorophosphonates
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
Yang et al. Stereoselective synthesis of (−)-centrolobine
Adams et al. Aminosugar motifs via an allene aziridination strategy
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
Yadav et al. Total synthesis of rhoiptelol B
Craig et al. Metal-Free Synthesis of Oxazinones and Their Reductive Ring Opening to Provide Cyclopropyl Carbinols
Yabuno et al. Site-and Stereoselectivity in the Photochemical Oxetane Formation Reaction (Paternò–Büchi Reaction) of Tetrahydrobenzofuranols with Benzophenone: Hydroxy-directed Diastereoselectivity?
Inoue et al. Symmetry-Driven Total Synthesis of Merrilactone A and Resolvin E2