Published: 2014-12-31

Editorial Board

Hakan Arslan

i-i

DOI: https://doi.org/10.5155/eurjchem.5.4.i-i.1163
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Graphical Contents

Hakan Arslan

ii-vii

DOI: https://doi.org/10.5155/eurjchem.5.4.ii-vii.1164
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Synthesis and evaluation of antibacterial activity for a series of N-phthaloylglycine derivatives

Samreen Begum, Shaikh Sirajuddin Nizami, Sumayya Saied, Syed Muhammad Shahid, Fatima Zehra Basha

557-562

DOI: https://doi.org/10.5155/eurjchem.5.4.557-562.1077
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DOI: https://doi.org/10.5155/eurjchem.5.4.563-569.1083
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Synthesis, characterization and in vitro biological evaluation of some new 1,3,5-triazine-chalcone hybrid molecules as Mycobacterium tuberculosis H37Rv inhibitors

Subbarayal Reddy Dwarampudi, Gowri Sankar Dannana, Vasudeva Rao Avupati, Venkata Satyanarayana Murthy Bendi

570-576

DOI: https://doi.org/10.5155/eurjchem.5.4.570-576.1098
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Study on regioselective synthesis of bioactive bis-spiropyrazolines using molecular orbital calculations

Thoraya Abd El-Reheem Farghaly, Ikhlass Mohamed Abbas, Walid Mohamed Ibrahim Hassan, Mai Samir Lotfy

577-583

DOI: https://doi.org/10.5155/eurjchem.5.4.577-583.1039
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Synthesis and study of antimicrobial activity of new tetralone esters

Krishna Mudeenahally Hucchegowda, Basavaraju Yeriyur Basavaiah, Umesha Basavaiah, Shivakumar Santhekasalagere Basavaiah

584-587

DOI: https://doi.org/10.5155/eurjchem.5.4.584-587.1093
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Synthesis, anti-HIV activity and molecular modeling study of some new pyrimidine analogues

Yossra Abood Marich, Niran Jassim Al-Salihi, Najim Aboud Al-Masoudi

588-594

DOI: https://doi.org/10.5155/eurjchem.5.4.588-594.1109
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Synthesis and antioxidant evaluation of some new sulphadimidine incorporating thiophene moiety

Moustafa Ahmed Gouda, Hadeer Fakhr Eldien, Margret Mansour Girges, Moged Ahmed Berghot

595-600

DOI: https://doi.org/10.5155/eurjchem.5.4.595-600.1106
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Synthesis and biological evaluation of shikimic acid derivatives

Van Hung Nguyen, Van Cuong Pham, Huong Doan Thi Mai, Thanh Nguyen Le, Thi Minh Hang Nguyen, Van Nam Vu, Huu Giap Tran, Thi Thao Do, Wim Dehaen, Van Minh Chau

601-606

DOI: https://doi.org/10.5155/eurjchem.5.4.601-606.1096
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DOI: https://doi.org/10.5155/eurjchem.5.4.607-611.1102
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FeCl3-catalysed C-N coupling reaction between cyclic ethers and heterocyclic amines

Suresh Mani, Mashood Ahamed Fazul Mohamed, Abdul Khader Karakkakal, Syed Ali Padusha Mohamed Khan

612-617

DOI: https://doi.org/10.5155/eurjchem.5.4.612-617.1108
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DOI: https://doi.org/10.5155/eurjchem.5.4.618-627.1089
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Synthesis and biological evaluation of new quinazolinone derivatives

Firyal Weli Asker, Salma Abdul Rudha Abbas, Redha Ibrahim Al-Bayati, Hanaa Abd Al-Tamemi

628-634

DOI: https://doi.org/10.5155/eurjchem.5.4.628-634.1120
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DOI: https://doi.org/10.5155/eurjchem.5.4.635-638.1131
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DOI: https://doi.org/10.5155/eurjchem.5.4.639-643.1126
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DOI: https://doi.org/10.5155/eurjchem.5.4.644-651.1125
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DOI: https://doi.org/10.5155/eurjchem.5.4.652-656.1100
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The effect of caffeine on some indicators of bone metabolism in rats

Hala Mohamed Mokhtar Abdelkarem, Nawal Abudall Al-Badr, Hanan Seleim Al-Naser

657-661

DOI: https://doi.org/10.5155/eurjchem.5.4.657-661.922
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DOI: https://doi.org/10.5155/eurjchem.5.4.662-667.1090
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β-Cyclodextrin catalyzed synthesis of substituted indoles in aqueous medium

Jilla Shankar, Gaddam Satish, Bandam Santosh Pavan Anil Kumar, Yadavalli Venkata Durga Nageswar

668-670

DOI: https://doi.org/10.5155/eurjchem.5.4.668-670.1085
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Synthesis of 2-aryl substituted 2,3-dihydroquinazoline-4(1H)-ones under solvent free conditions using ionic liquid as a mild and efficient catalyst

Obaiah Obaiah, Nandeesh Nagalingaiah Kebbahalli, Raghavendra Manchigaiah Goravanahalli, Pavankumar Siddalingaiah Chottanahalli, Rangappa Subbegowda Kanchugarakoppal, Mantelingu Kempegowda

671-675

DOI: https://doi.org/10.5155/eurjchem.5.4.671-675.1071
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DOI: https://doi.org/10.5155/eurjchem.5.4.676-680.1110
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Synthesis, reactions and applications of pyranotriazolopyrimidines

Ashraf Hassan Fekry Abd El-Wahab, Ibrahim Ali Radini, Hany Mostafa Mohamed

681-694

DOI: https://doi.org/10.5155/eurjchem.5.4.681-694.1087
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DOI: https://doi.org/10.5155/eurjchem.5.4.695-696.1119
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