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   <subfield code="a">10.1007/s12039-013-0371-4</subfield>
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   <subfield code="a">Synthesis, characterization and antimicrobial screening of hybrid molecules containing quinoline, pyrimidine and morpholine analogues</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[N DESAI, K RAJPARA, V JOSHI, H VAGHANI, H SATODIYA]</subfield>
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   <subfield code="a">In an attempt to find new bio-active molecules, a series of compounds N-(4-(2-chloroquinolin-3-yl)-6-(aryl)pyrimidin-2-yl)-2-morpholinoacetamides (5a-l) were synthesized by multistep reactions. Compounds were characterized by IR, NMR and mass spectra. Antimicrobial screening of title compounds (5a-l) was carried out against Gram-positive bacteria (Staphylococcus aureus, Streptococcus pyogenes), Gram-negative bacteria (Escherichia coli, Pseudomonas aeruginosa) and fungi (Candida albicans, Aspergillus niger, Aspergillus clavatus) using serial broth dilution method. On the basis of statistical analysis, it is observed that these compounds gave significant co-relation. Newly synthesized compounds 5e, 5f, 5g, 5i and 5l showed significant potency against different microbial strains. Graphical Abstract A novel series of compounds N-(4-(2-chloroquinolin-3-yl)-6-(aryl)pyrimidin-2-yl)-2-morpholinoacetamides (5a-l) were synthesized by multi-step reactions. Newly synthesized compounds were characterized by various spectroscopic techniques and screened for in vitro antimicrobial activity.</subfield>
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   <subfield code="a">Indian Academy of Sciences, 2013</subfield>
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   <subfield code="a">DESAI</subfield>
   <subfield code="D">N.</subfield>
   <subfield code="u">Division of Medicinal Chemistry, Department of Chemistry (DST-FIST Sponsored Department), Mahatma Gandhi Campus, Maharaja Krishnakumarsinhji Bhavnagar University, 364 002, Bhavnagar, dnisheeth@rediffmail.com, India</subfield>
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   <subfield code="u">Division of Medicinal Chemistry, Department of Chemistry (DST-FIST Sponsored Department), Mahatma Gandhi Campus, Maharaja Krishnakumarsinhji Bhavnagar University, 364 002, Bhavnagar, dnisheeth@rediffmail.com, India</subfield>
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   <subfield code="u">Division of Medicinal Chemistry, Department of Chemistry (DST-FIST Sponsored Department), Mahatma Gandhi Campus, Maharaja Krishnakumarsinhji Bhavnagar University, 364 002, Bhavnagar, dnisheeth@rediffmail.com, India</subfield>
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   <subfield code="u">Division of Medicinal Chemistry, Department of Chemistry (DST-FIST Sponsored Department), Mahatma Gandhi Campus, Maharaja Krishnakumarsinhji Bhavnagar University, 364 002, Bhavnagar, dnisheeth@rediffmail.com, India</subfield>
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   <subfield code="u">Division of Medicinal Chemistry, Department of Chemistry (DST-FIST Sponsored Department), Mahatma Gandhi Campus, Maharaja Krishnakumarsinhji Bhavnagar University, 364 002, Bhavnagar, dnisheeth@rediffmail.com, India</subfield>
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   <subfield code="t">Journal of Chemical Sciences</subfield>
   <subfield code="d">Springer-Verlag</subfield>
   <subfield code="g">125/2(2013-03-01), 321-333</subfield>
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   <subfield code="u">Division of Medicinal Chemistry, Department of Chemistry (DST-FIST Sponsored Department), Mahatma Gandhi Campus, Maharaja Krishnakumarsinhji Bhavnagar University, 364 002, Bhavnagar, dnisheeth@rediffmail.com, India</subfield>
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   <subfield code="u">Division of Medicinal Chemistry, Department of Chemistry (DST-FIST Sponsored Department), Mahatma Gandhi Campus, Maharaja Krishnakumarsinhji Bhavnagar University, 364 002, Bhavnagar, dnisheeth@rediffmail.com, India</subfield>
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