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Synthesis of Highly Substituted Fluoro Chromenones in a " One‐Pot Four‐ Component Strategy " Using NFSI as a Fluorinating Reagent.
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- ChemistrySelect, 2019, v. 4, n. 47, p. 13768, doi. 10.1002/slct.201904090
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- Article
Design and Synthesis of Novel Pyrimidine/Hexahydroquinazoline‐Fused Pyrazolo[3,4‐b]Pyridine Derivatives, Their Biological Evaluation and Docking Studies<sup>#</sup>.
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- ChemistrySelect, 2019, v. 4, n. 1, p. 138, doi. 10.1002/slct.201803078
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- Article
Synthesis of Novel Pyrido[2′, 3′:3,4]Pyrazolo[1, 5‐a]Quinazoline Derivatives, Their Biological Evaluation and Molecular Modelling Studies.
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- ChemistrySelect, 2018, v. 3, n. 27, p. 7813, doi. 10.1002/slct.201801186
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- Article
Regioselective Synthesis of 2‐(Trifluoromethyl)‐3‐ethoxycarbonyl‐4‐(2‐oxo‐2‐arylethyl)‐4H‐chromene Derivatives by [3, 3] Sigmatropic Rearrangement.
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- ChemistrySelect, 2017, v. 2, n. 35, p. 11545, doi. 10.1002/slct.201701723
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Studies on Synthesis of Novel Pyrido[2,3‐d] pyrimidine Derivatives and Their Anticancer Activity.
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- Journal of Heterocyclic Chemistry, 2018, v. 55, n. 11, p. 2538, doi. 10.1002/jhet.3307
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- Article
Synthesis of Novel Diverse Methoxybenzenes-substituted 2 H/4 H-chromene Derivatives in the Presence of InBr<sub>3</sub> (5 mol%) and their Cytotoxic Activity.
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- Journal of Heterocyclic Chemistry, 2017, v. 54, n. 6, p. 3607, doi. 10.1002/jhet.2987
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- Article
Synthesis and Anticancer Activity of Novel N-trisazole/isoxazole Alkyl Functionalized Quinolin-2(1 H)-one Derivatives.
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- Journal of Heterocyclic Chemistry, 2017, v. 54, n. 1, p. 194, doi. 10.1002/jhet.2566
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- Article
Synthesis of Novel 1,2,3-Triazole/Isoxazole-Functionalized Imidazo[4,5- b]pyridin-2(3H)-one Derivatives, Their Antimicrobial and Anticancer Activity.
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- Journal of Heterocyclic Chemistry, 2016, v. 53, n. 4, p. 1168, doi. 10.1002/jhet.2370
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- Article
Synthesis of α‐Fluoroamides with a C–F Quaternary Stereogenic Center by Electrophilic Fluorination: One‐Pot Four‐Component Strategy.
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- European Journal of Organic Chemistry, 2019, v. 2019, n. 22, p. 3654, doi. 10.1002/ejoc.201900482
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- Article
Gem‐Difluorination of Triazole Alkyl Functionalized Amino Pyrazoles by Selectfluor to Access 4,4‐Difluoro‐pyrazol‐3‐ones/Pyrazol‐3‐imines.
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- European Journal of Organic Chemistry, 2019, v. 2019, n. 13, p. 2409, doi. 10.1002/ejoc.201900173
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- Article
Selectfluor-Mediated Synthesis of Fluoro Spiro 3(2H)-Furanone Derivatives via Domino Fluorination-Defluorination.
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- European Journal of Organic Chemistry, 2018, v. 2018, n. 3, p. 413, doi. 10.1002/ejoc.201701668
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An Efficient One-Pot Synthesis of Substituted 1 H-Naphtho[2,1- b]pyrans and 4 H-1-Benzopyrans (=Chromenes) under Solvent-Free Microwave-Irradiation Conditions.
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- Helvetica Chimica Acta, 2012, v. 95, n. 3, p. 502, doi. 10.1002/hlca.201100332
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CuBr/FeCl<sub>3</sub> Catalysis: a Novel and Efficient Method for the Preparation of New Aryl (Iminomethyl)propargyl Ether Derivatives via CH Activation of Aryl Propargyl Ethers.
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- Helvetica Chimica Acta, 2011, v. 94, n. 9, p. 1692, doi. 10.1002/hlca.201100072
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Synthesis of Novel Pyrido[3,2- e][1,2,4]triazolo[1,5- c]pyrimidine Derivatives: Potent and Selective Adenosine A<sub>3</sub> Receptor Antagonists.
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- Archiv der Pharmazie, 2013, v. 346, n. 10, p. 699, doi. 10.1002/ardp.201300003
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- Article