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References from Total Synthesis of Nocarterphenyls A-B and 2-Dehydroxymethylnocarterphenyl A, Formal Synthesis of Nocarterphenyl D, and Biological Evaluation of Nocarterphenyls as α-Glucosidase Inhibitors. Local targets link to admitted publications; unresolved targets remain external evidence.
Structural and biological diversity of natural p-terphenyls
10.1080/10286020.2017.1381089 · 2018 · External reference
Structural diversity and biological activity of natural p-terphenyls
10.1007/s42995-021-00117-8 · 2022 · External reference
DPPH Radical Scavenging Activity of Ten Natural p-Terphenyl Derivatives Obtained from Three Edible Mushrooms Indigenous to China
10.1002/cbdv.200490050 · 2004 · External reference
Anticancer Activities of Thelephantin O and Vialinin A Isolated from Thelephora aurantiotincta
10.1021/jf200461j · 2011 · External reference
Isolation and Characterization of New p-Terphenyls with Antifungal, Antibacterial, and Antioxidant Activities from Halophilic Actinomycete Nocardiopsis gilva YIM 90087
10.1021/jf400718w · 2013 · External reference
Design, semisynthesis, α-glucosidase inhibitory, cytotoxic, and antibacterial activities of p-terphenyl derivatives
10.1016/j.ejmech.2018.01.057 · 2018 · External reference
p-Terphenyls From Aspergillus sp GZWMJZ-055: Identification, Derivation, Antioxidant and α-Glycosidase Inhibitory Activities
10.3389/fmicb.2021.654963 · 2021 · External reference
β-Secretase (BACE1) inhibitory and neuroprotective effects of p-terphenyls from Polyozellus multiplex
10.1039/c6fo00538a · 2016 · External reference
p-Terphenyl O-β-glucuronides, DNA topoisomerase inhibitors from Streptomyces sp LZ35ΔgdmAI
10.1016/j.bmcl.2014.01.037 · 2014 · External reference
Cytotoxic p-Terphenyls from a Marine-Derived Nocardiopsis Species
10.1021/acs.jnatprod.9b00963 · 2019 · External reference
Antibacterial p-Terphenyl with a Rare 2,2′-Bithiazole Substructure and Related Compounds Isolated from the Marine-Derived Actinomycete Nocardiopsis sp HDN154086
10.1021/acs.jnatprod.0c01296 · 2021 · External reference
Antibacterial p-terphenyl and α-pyrone derivates isolated from the marine-derived actinomycete Nocardiopsis sp HDN154086
10.1038/s41429-023-00698-9 · 2024 · External reference
Semisynthesis of Nocarterphenyl A and Its Analogues
10.1021/acs.jnatprod.4c01198 · 2025 · External reference
Total Synthesis of Nocarterphenyl A
10.1002/slct.202501946 · 2025 · External reference
Total Synthesis of Nocarterphenyl A, 2-Dehydroxymethylnocarterphenyl A and Nocarterphenyl D Produced by Marine Nocardiopsis spp
10.1021/acs.jnatprod.5c01038 · 2025 · External reference
Total Synthesis of Asperphenins A and B
10.1021/acs.orglett.8b02652 · 2018 · External reference
Towards the total synthesis of mandelalide B: construction of the tetrahydrofuran/α-hydroxyl lactone fragment
10.1039/d4qo01433b · 2024 · External reference
Total Synthesis of the Marine Cyclic Depsipeptide Lagunamide D
10.3390/md23030099 · 2025 · External reference
Second-Generation Synthesis of Psymberin
10.1021/acs.orglett.5c00396 · 2025 · External reference
Synthesis and anti-α-glucosidase activity evaluation of betulinic acid derivatives
10.1016/j.arabjc.2023.104659 · 2023 · External reference
Synthesis and biological evaluation of coumarin derivatives as α-glucosidase inhibitors
10.1016/j.ejmech.2019.112013 · 2020 · External reference
Investigation on the inhibition mechanism and binding behavior of cryptolepine to α-glucosidase and its hypoglycemic activity by multi-spectroscopic method
10.1016/j.jlumin.2024.120437 · 2024 · External reference
Identification of 1,3,4-Thiadiazolyl-Containing Thiazolidine-2,4-dione Derivatives as Novel PTP1B Inhibitors with Antidiabetic Activity
10.1021/acs.jmedchem.4c00676 · 2024 · External reference
Molecular Mechanism in α-Glucosidase and Glucoamylase
10.1271/bbb.61.1233 · 1997 · External reference
Unresolved reference
2004 · External reference
Recent Advances in Synthetic α-Glucosidase Inhibitors
10.1002/cmdc.201700216 · 2017 · External reference
10.1002/9781119785033.ch11
10.1002/9781119785033.ch11 · 2022 · External reference
Efficacy and safety of voglibose in comparison with acarbose in type 2 diabetic patients
10.1016/s0168-8227(01)00286-8 · 2002 · External reference
2,5-Disubstituted furan derivatives containing 1,3,4-thiadiazole moiety as potent α-glucosidase and E coli β-glucuronidase inhibitors
10.1016/j.ejmech.2021.113322 · 2021 · External reference
The Palladium-Catalyzed Cross-Coupling Reaction of Phenylboronic Acid with Haloarenes in the Presence of Bases
10.1080/00397918108063618 · 1981 · External reference
Palladium-Catalyzed Cross-Coupling Reactions of Organoboron Compounds
10.1021/cr00039a007 · 1995 · External reference
First Total Synthesis of Vialinin A, a Novel and Extremely Potent Inhibitor of TNF-α Production
10.1021/ol701590b · 2007 · External reference
Structural Revision of Thelephantin G by Total Synthesis and the Inhibitory Activity against TNF-α Production
10.1021/jo900638b · 2009 · External reference
Structural revision of kynapcin-12 by total synthesis, and inhibitory activities against prolyl oligopeptidase and cancer cells
10.1016/j.bmcl.2014.05.091 · 2014 · External reference
Construction of aromatic-ring-layered structures using a terphenylene-layered polymer as the scaffold
10.1039/c3py00607g · 2013 · External reference
Tuning the Hydrophobicity of Zinc Dipyridyl Paddlewheel Metal–Organic Frameworks for Selective Sorption
10.1021/cg400342m · 2013 · External reference
Synthesis of cyclic compounds consisting of face-to-face p-oligophenyls
10.1016/j.tetlet.2014.01.093 · 2014 · External reference
K2S as Sulfur Source and DMSO as Carbon Source for the Synthesis of 2-Unsubstituted Benzothiazoles
10.1021/acs.orglett.0c00994 · 2020 · External reference
Double C–S bond formation via C–H bond functionalization: synthesis of benzothiazoles and naphtho[2,1-d]thiazoles from N-substituted arylamines and elemental sulfur
10.1039/c7cc07366f · 2017 · External reference
An expeditious and general aromatic iodination procedure
10.1039/c39920001016 · 1992 · External reference
Acid-mediated reaction of bis(pyridine)iodonium(I) tetrafluoroborate with aromatic compounds A selective and general iodination method
10.1021/jo00060a020 · 1993 · External reference
Direct C2-Alkylation of Azoles with Alcohols and Ethers through Dehydrogenative Cross-Coupling under Metal-Free Conditions
10.1021/ol201779n · 2011 · External reference
Opening of cyclic acetals by trichloro-, dichloro-, and tribromo-borane
10.1039/p19810001807 · 1981 · External reference
Conversion of methylenedioxybenzene derivatives into 2-methoxyphenol derivatives
10.3987/r-1983-11-2237 · 1983 · External reference
A Novel B(C6F5)3-Catalyzed Reduction of Alcohols and Cleavage of Aryl and Alkyl Ethers with Hydrosilanes
10.1021/jo000726d · 2000 · External reference
Regioselective cleavage of the methylenedioxy group: conversion of (-)-austrobailignan-5 to (-)-dihydroguaiaretic acid
10.1021/jo00292a010 · 1990 · External reference
Cleavage of Catechol Monoalkyl Ethers by Aluminum Triiodide–Dimethyl Sulfoxide
10.1055/s-0037-1610996 · 2019 · External reference
Anchimerically Assisted Selective Cleavage of Acid-Labile Aryl Alkyl Ethers by Aluminum Triiodide and N,N-Dimethylformamide Dimethyl Acetal
10.1021/acs.joc.0c00290 · 2020 · External reference
NIS–PPh3: A Selective Reagent for the Spiroannulation of o-Allyl Phenols. Total Synthesis of Corallidictyal D
10.1021/jo4014047 · 2013 · External reference
Study on the metabolism of 5,6-methylenedioxy-2-aminoindane (MDAI) in rats: identification of urinary metabolites
10.1080/00498254.2016.1199919 · 2017 · External reference
Anchimerically Assisted Cleavage of Aryl Methyl Ethers by Aluminum Chloride-Sodium Iodide in Acetonitrile
10.1002/slct.201802565 · 2018 · External reference
Synthesis of Rotundine
2012 · External reference
The Constituents of Schizandra chinensis BAILL. IX The Cleavage of the Methylenedioxyl Moiety with Lead Tetraacetate in Benzene, and the Structure of Angeloylgomisin Q
10.1248/cpb.29.2893 · 1981 · External reference
Mild and regioselective iodination of electron-rich aromatics with N-iodosuccinimide and catalytic trifluoroacetic acid
10.1016/s0040-4039(02)01010-9 · 2002 · External reference
Synthetic methods and reactions. 181 Iodination of deactivated aromatics with N-iodosuccinimide in trifluoromethanesulfonic acid (NIS-CF3SO3H) via in situ generated superelectrophilic iodine(I) trifluoromethanesulfonate
10.1021/jo00063a052 · 1993 · External reference
Triiodoisocyanuric acid: a new and convenient reagent for regioselective coiodination of alkenes and enolethers with oxygenated nucleophiles
10.1016/j.tetlet.2007.10.011 · 2007 · External reference
A mild and simple iodination of phenols with trichloroisocyanuric acid/ I2 /Wet SiO2 system
10.1590/s0103-50532010000100002 · 2010 · External reference
N-Bromosuccinimide-dimethylformamide: a mild, selective nuclear monobromination reagent for reactive aromatic compounds
10.1021/jo00393a066 · 1979 · External reference
Brominations conducted with pyridinium bromide perbromide
10.1021/jo01158a013 · 1949 · External reference
The use of pyridinium bromide perbromide for brominations
10.1021/ed026p613 · 1949 · External reference
Pd-Complex Catalyzed Suzuki Cross-Coupling Reaction of Brominated Salicylaldehyde with Pyridylboronic Acid
10.6023/cjoc201407024 · 2014 · External reference
Virtual Screening and Multistage Computational Profiling of Small-Molecule Inhibitors Targeting Clostridioides difficile Toxin B
10.1021/acs.jmedchem.5c01483 · 2025 · External reference
Structure-based drug design of an inhibitor of the SARS-CoV-2 (COVID-19) main protease using free software: A tutorial for students and scientists
10.1016/j.ejmech.2021.113390 · 2021 · External reference
Discovery of Novel PROTAC SIRT6 Degraders with Potent Efficacy against Hepatocellular Carcinoma
10.1021/acs.jmedchem.4c01223 · 2024 · External reference
