A Straightforward Synthesis of Pinocembrin

• Material Type: 記事
• Title: A Straightforward Synthesis of Pinocembrin
• Author Heading: Iwai Kento; https://orcid.org/0000-0002-0923-604X; Nishiwaki Nagatoshi; https://orcid.org/0000-0002-6052-8697
• Publication Date: 2025
• Publication Date (W3CDTF): 2025
• Periodical title: Journal of Oleo Science
• No. or year of volume/issue: 74 1
• Volume: 74
• Issue: 1
• Pages: 75-78
• Publication date of volume/issue (W3CDTF): 2025
• ISSN (Periodical Title): 13458957
• ISSN-L (Periodical Title): 13458957
• Publication (Periodical Title): Japan Oil Chemists' Society
• Text Language Code: en
• Subject Heading: flavanone; intramolecular conjugate addition; protection-free
• Target Audience: 一般
• Standard No. (Other): PMID : 39756994
• DOI: 10.5650/jos.ess24245
• Related Material (URI): http://hdl.handle.net/10935/0002006089; https://nara-wu.repo.nii.ac.jp/records/2006089; https://www.jstage.jst.go.jp/article/jos/74/1/74_ess24245/_pdf
• References: Facile Formation of Methylenebis(chalcone)s through Unprecedented Methylenation Reaction. Application to Antiparasitic and Natural Product Synthesis; https://cir.nii.ac.jp/crid/1360021800065558784; Mechanical and aesthetics compatibility of Brazilian red propolis micellar nanocomposite as a cavity cleaning agent; https://cir.nii.ac.jp/crid/1360021800066578688; Efficient production of (2S)-flavanones by Escherichia coli containing an artificial biosynthetic gene cluster; https://cir.nii.ac.jp/crid/1360292618857894656; Chrysin: Sources, beneficial pharmacological activities, and molecular mechanism of action; https://cir.nii.ac.jp/crid/1360292621315564544; Synthesis and Antidiabetic Activity of 5,7‐Dihydroxyflavonoids and Analogs; https://cir.nii.ac.jp/crid/1360303275225520768; Pinocembrin improves cognition and protects the neurovascular unit in Alzheimer related deficits; https://cir.nii.ac.jp/crid/1360303275226050176; Advances in Biosynthesis, Pharmacology, and Pharmacokinetics of Pinocembrin, a Promising Natural Small-Molecule Drug; https://cir.nii.ac.jp/crid/1360303275243372672; Design, synthesis, and cholinesterase inhibition assay of liquiritigenin derivatives as anti-Alzheimer's activity; https://cir.nii.ac.jp/crid/1360303275734364800; An Efficient Synthesis of Neoflavonoid Antioxidants Based on Montmorillonite K-10 Catalysis; https://cir.nii.ac.jp/crid/1360303275734443136; Antifibrotic Mechanism of Pinocembrin: Impact on Oxidative Stress, Inflammation and TGF-β /Smad Inhibition in Rats; https://cir.nii.ac.jp/crid/1360303275734707968; Plant flavonoids in cancer chemoprevention: role in genome stability; https://cir.nii.ac.jp/crid/1360574094744721536; Biosynthesis of Pinocembrin from Glucose Using Engineered Escherichia coli; https://cir.nii.ac.jp/crid/1360579816257096448; Synthesis and characterization of 5,7-dihydroxyflavanone derivatives as novel protein tyrosine phosphatase 1B inhibitors; https://cir.nii.ac.jp/crid/1360580234551031296; Total Synthesis and Antibacterial Evaluation of Lupinifolin and Its Natural Analogues; https://cir.nii.ac.jp/crid/1360584750558611968; Photochemical synthesis of 2'-hydroxychalcones from phenyl cinnamates; https://cir.nii.ac.jp/crid/1360584750558701696; Phenolic Compounds in Honey and Their Associated Health Benefits: A Review; https://cir.nii.ac.jp/crid/1360584750559641984; Cytotoxicity of dietary flavonoids on different human cancer types; https://cir.nii.ac.jp/crid/1360855569818426368; Heterologous Biosynthesis of Health-Promoting Baicalein in Lycopersicon esculentum; https://cir.nii.ac.jp/crid/1360866225192804480; Synthesis of Antimicrobial Natural Products Targeting FtsZ: (±)-Dichamanetin and (±)-2‘ ‘‘-Hydroxy-5‘ ‘-benzylisouvarinol-B; https://cir.nii.ac.jp/crid/1361699994260509312; Synthesis of 4,8-dimethoxy-1-naphthol via an acetyl migration; https://cir.nii.ac.jp/crid/1362544418359126144
• Data Provider (Database): 国立情報学研究所 : CiNii Research; https://cir.nii.ac.jp/
• Original Data Provider (Database): Japan Link Center; https://japanlinkcenter.org/top; 学術機関リポジトリデータベース; https://irdb.nii.ac.jp; Crossref; https://www.crossref.org; PubMed; https://pubmed.ncbi.nlm.nih.gov

• Summary, etc.: <p>A simple synthetic method for pinocembrin from cinnamic acid and 1,3,5-trihydroxybenzene was provided. This method can be performed in one-pot two ...