about
The antihyperlipidemic activities of 4(3H) quinazolinone and two halogenated derivatives in rats.Synthetic Strategies for 5- and 6-Membered Ring Azaheterocycles Facilitated by Iminyl RadicalsChemical characteristics, synthetic methods, and biological potential of quinazoline and quinazolinone derivatives.Benzodiazines: recent synthetic advances.2-alkyl(aryl)-quinazolin-4(3H)-thiones, 2-R-(quinazolin-4(3H)-ylthio)carboxylic acids and amides: synthesis, molecular docking, antimicrobial and anticancer properties.Synthesis and Antimicrobial Screening of Pyrazolo-3-Aryl Quinazolin-4(3H)ones.2-(4-Chloro-phen-yl)-4-phenyl-1,2-di-hydro-quinazoline.Possible inhibition of hydroxy methyl glutaryl CoA reductase activity by nicotinic acid and ergosterol: as targeting for hypocholesterolemic actionSynthesis and biological evaluation of cationic fullerene quinazolinone conjugates and their binding mode with modeled Mycobacterium tuberculosis hypoxanthine-guanine phosphoribosyltransferase enzyme.Molecular docking and biological evaluation of some thioxoquinazolin-4(3H)-one derivatives as anticancer, antioxidant and anticonvulsant agents.Copper-catalyzed annulation of amidines for quinazoline synthesis.Pd(0)-catalyzed benzylic arylation-oxidation of 4-methylquinazolines via sp3 C-H activation under air conditions.Lewis Acid Catalyzed Condensation-Cyclization Cascade: Direct Synthesis of Di/Trifluoromethyl-1,2,3,4-tetrahydroquinazolines.Iron-catalyzed cascade reaction of 2-aminobenzyl alcohols with benzylamines: synthesis of quinazolines by trapping of ammonia.Synthesis of quinazolines and tetrahydroquinazolines: copper-catalyzed tandem reactions of 2-bromobenzyl bromides with aldehydes and aqueous ammonia or amines.One-pot three-component synthesis of quinazolines via a copper-catalysed oxidative amination reaction.
P2860
Q24816874-F40C140C-6769-4A67-974F-1120FBBFA615Q26746980-BAA9E5D5-A4C2-408E-8BFF-E5D126BCF01AQ38359825-2AEF966E-1CA4-4304-84D2-1E8861A1FE2EQ39269222-59F24689-BAE5-4CD0-B9B6-0AC069DBFF46Q41128751-9CEA09D9-2DFD-4C0E-A2AF-56992520AADFQ41576842-A1DEDFF1-BA7C-4523-976E-37FEE100585BQ41857534-A83E5A18-6B4F-4E80-A08B-DCEBBD7467F2Q42034607-48D07564-CC9B-4F82-99B2-500539D20C13Q42711627-7CB736AD-3C25-478C-A7AE-8C24BB4A0E66Q42813308-F5F0013E-63A2-458D-B067-DDA828842BF0Q44598718-4C346A7F-9113-4F2A-8C21-EB0FC8647B09Q44794759-746FEBC2-2055-485E-BDD0-4716FA17D0F5Q46072881-41DA0D14-1949-4750-94D3-C539A78DFABFQ48205758-86DBEA7D-5D49-440A-B98A-208C2682140DQ50464862-6DCFB6F3-1E38-485E-AC8D-D9AF2C5DB4C1Q51291086-59D27E2F-5E1D-4B57-8C4D-26DCEC31BB1B
P2860
description
2000 nî lūn-bûn
@nan
2000 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
2000 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
2000年の論文
@ja
2000年論文
@yue
2000年論文
@zh-hant
2000年論文
@zh-hk
2000年論文
@zh-mo
2000年論文
@zh-tw
2000年论文
@wuu
name
Quinazoline derivatives with antitubercular activity.
@ast
Quinazoline derivatives with antitubercular activity.
@en
type
label
Quinazoline derivatives with antitubercular activity.
@ast
Quinazoline derivatives with antitubercular activity.
@en
prefLabel
Quinazoline derivatives with antitubercular activity.
@ast
Quinazoline derivatives with antitubercular activity.
@en
P2093
P1433
P1476
Quinazoline derivatives with antitubercular activity.
@en
P2093
P304
P356
10.1016/S0014-827X(00)00100-2
P577
2000-11-01T00:00:00Z