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3-dihydrobenzofuran (7) 7
index medicus (6) 6
chemistry, multidisciplinary (5) 5
2,3-dihydrobenzofuran (4) 4
chemistry, medicinal (4) 4
benzofuran (3) 3
chemical sciences (3) 3
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by Yang, WQ and Liu, YY and Zhang, SS and Cai, Q
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, ISSN 1433-7851, 07/2015, Volume 54, Issue 30, pp. 8805 - 8808
O-Heterocyclic structures such as 2,3-dihydrobenzofurans are key motifs in many natural compounds and pharmaceuticals. Enantioselective formation of chiral... 
SILYL PROTECTION | PALLADIUM | desymmetrization | ASYMMETRIC-SYNTHESIS | TERT-ALKYLAMINES | 3-dihydrobenzofuran | ANALOGS | NATURAL-PRODUCTS | O-arylation | BOND FORMATION | OLEFIN METATHESIS | asymmetric catalysis | CHEMISTRY, MULTIDISCIPLINARY | ALCOHOLS | copper | CYCLIZATION
Journal Article
Advanced Synthesis & Catalysis, ISSN 1615-4150, 06/2019, Volume 361, Issue 11, pp. 2696 - 2705
The laccase‐catalyzed oxidation of a series of substituted 4‐hydroxy‐chalcones has been investigated. The main isolated dimeric products were, as expected,... 
Chalcones | Oxidation | Biocatalysis | 2,3-Dihydrobenzofuran | Laccase | RESVERATROL | ANTIOXIDANT | 3-Dihydrobenzofuran | CHEMISTRY, ORGANIC | DIMERIZATION | CHALCONE | CHEMISTRY, APPLIED | Oxidases | Enantiomers | Oxidation-reduction reaction | Dimers | Molecular structure | Column chromatography
Journal Article
Journal Article
Bioorganic & Medicinal Chemistry, ISSN 0968-0896, 02/2016, Volume 24, Issue 4, pp. 820 - 826
[Display omitted] 2,3-Dihydrobenzofurans are proposed as privileged structures and used as chemical platform to design small compound libraries. By combining... 
mPGES-1 inhibitors | Inflammation | 2,3-Dihydrobenzofuran privileged structure | Molecular docking | Cancer | DRUG | ANTIBIOTICS | CHEMISTRY, MEDICINAL | FURAQUINOCIN-B | BIOCHEMISTRY & MOLECULAR BIOLOGY | COMBINATORIAL LIBRARIES | CHEMISTRY, ORGANIC | IDENTIFICATION | DISCOVERY | PROSTAGLANDIN E-2 SYNTHASE-1 | POTENT | 5-LIPOXYGENASE | DERIVATIVES | Proto-Oncogene Proteins c-met - metabolism | Antineoplastic Agents - chemical synthesis | Epithelial Cells - drug effects | Humans | Molecular Sequence Data | Benzofurans - pharmacology | Structure-Activity Relationship | Enzyme Inhibitors - chemical synthesis | Anti-Inflammatory Agents, Non-Steroidal - pharmacology | Microsomes - drug effects | Drug Design | Inhibitory Concentration 50 | Antineoplastic Agents - pharmacology | Intramolecular Oxidoreductases | Anti-Inflammatory Agents, Non-Steroidal - chemical synthesis | Epithelial Cells - cytology | Cell Survival - drug effects | Gene Expression | Protein Structure, Secondary | Proto-Oncogene Proteins c-met - antagonists & inhibitors | Enzyme Inhibitors - pharmacology | Benzofurans - chemical synthesis | Microsomes - enzymology | Amino Acid Motifs | Proto-Oncogene Proteins c-met - genetics | Prostaglandin-E Synthases | Epithelial Cells - enzymology | Cell Line, Tumor | Molecular Docking Simulation | Proto-Oncogene Proteins c-met - chemistry | Drug Screening Assays, Antitumor | Biomimetics | Lead compounds | Life Sciences | Chemical Sciences
Journal Article
Chemical and Pharmaceutical Bulletin, ISSN 0009-2363, 1989, Volume 37, Issue 9, pp. 2361 - 2368
Journal Article
Phytochemistry, ISSN 0031-9422, 1977, Volume 16, Issue 6, pp. 745 - 748
Seven neolignans, isolated from a C 6H 6 extract of Nectandra miranda (Lauraceae) trunk wood, included the hitherto undescribed (2 S, 3 S, 3a S)- and (2 S, 3... 
licarin-C | (2 S, 3 S, 3a S)-, (2 S, 3 S, 3a R)- and (2 R, 3 S, 3a S)-5-allyl-3a-methoxy-2-(3′, 4′, 5′-trimethoxyphenyl)-3- methyl-2, 3, 3a, 6-tetrahydro-6-oxobenzofuran | Nectandra miranda | neolignans | 7-allyl-6-hydroxy-5- methoxy-2-(3′, 4′, 5′-trimethoxyphenyl)-3-methylbenzofuran | (2 S, 3 S)-6- O-allyl-5-methoxy-2-(3′, 4′, 5′-trimethoxyphenyl)-3-methyl-2, 3-dihydrobenzofuran | (2 S, 3 S 5 R)-5-allyl-5-methoxy-2-(3′, 4′, 5′-trimethoxyphenyl)-3-methyl-2, 3, 5, 6-tetrahydro-6-oxobenzofuran | mirandin-A | mirandin-B | Lauraceae | (2 R, 3 R)-7-methoxy-2-(3′, 4′, 5′-trimethoxyphenyl)3-methyl-5-( E)-propenyl-2, 3-dihydrobenzofuran | (2 S, 3 S, 3a S)-3a-allyl-5-methoxy-2-(3′, 4′, 5′-trimethoxyphenyl)-3-methyl-2, 3, 3a, 6 tetrahydro-6-oxobenzofuran | (2S, 3S, 3aS)-, (2S, 3S, 3aR)- and (2R, 3S, 3aS)-5-allyl-3a-methoxy-2-(3′, 4′, 5′-trimethoxyphenyl)-3- methyl-2, 3, 3a, 6-tetrahydro-6-oxobenzofuran | (2S, 3S 5R)-5-allyl-5-methoxy-2-(3′, 4′, 5′-trimethoxyphenyl)-3-methyl-2, 3, 5, 6-tetrahydro-6-oxobenzofuran | (2S, 3S, 3aS)-3a-allyl-5-methoxy-2-(3′, 4′, 5′-trimethoxyphenyl)-3-methyl-2, 3, 3a, 6 tetrahydro-6-oxobenzofuran | (2R, 3R)-7-methoxy-2-(3′, 4′, 5′-trimethoxyphenyl)3-methyl-5-(E)-propenyl-2, 3-dihydrobenzofuran | (2S, 3S)-6-O-allyl-5-methoxy-2-(3′, 4′, 5′-trimethoxyphenyl)-3-methyl-2, 3-dihydrobenzofuran
Journal Article
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