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10.1007/s00706-013-1067-7 http://scihub22266oqcxt.onion/10.1007/s00706-013-1067-7 C4495853!4495853!26166876     free     free     free Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534       Monatsh+Chem 2013 ; 144 (11): 1679-89 Nephropedia Template TP {{tp|p=26166876|t=2013. Microwave-assisted preparation and antimicrobial activity of O-alkylamino benzofurancarboxylates |pdf=|usr=}}{{26166876}} gab.com Text Microwave-assisted preparation and antimicrobial activity of O-alkylamino benzofurancarboxylates JO: Monatsh Chem http://www.kidney.de/pget.php?&tw=1&pmid=26166876 #FOAvip Abstract: A series of derivatives of 2 and 3-benzofurancarboxylates were synthesized under microwave-assisted conditions. Their in-vitro antimicrobial properties were assessed. Inhibition by the compounds of the growth of antibiotic-susceptible standards and clinically isolated strains of Gram-positive and Gram-negative bacteria, yeasts, and a human fungal pathogen was moderate to significant. Methyl 5-bromo-7-[2-(N,N-diethylamino)ethoxy]-6-methoxy-2-benzofurancarboxylate hydrochloride was identified as the most active compound (MIC 3?12 × 10?3 ?mol/cm3 against Gram-positive bacteria; MIC 9.4 × 10?2 ?mol/cm3 against Candida and Aspergillus brasiliensis). The molecular and crystal structures of 2-(N,N-diethylamino)ethyl 6-acetyl-5-hydroxy-2-methyl-3-benzofurancarboxylate were established by single-crystal X-ray diffraction. Graphical Abstract: . Twit Text FOAVip Microwave-assisted preparation and antimicrobial activity of O-alkylamino benzofurancarboxylates ????Monatsh Chem http://www.kidney.de/pget.php?&tw=1&pmid=26166876 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=26166876 #FOAvip English Wikipedia <ref>{{Cite pmid|26166876}}</ref> Microwave-assisted preparation and antimicrobial activity of O-alkylamino benzofurancarboxylates #MMPMID26166876 Ostrowska K; Hejchman E; Wolska I; Kruszewska H; Maciejewska D Monatsh Chem 2013[]; 144 (11): 1679-89 PMID26166876show ga Abstract: A series of derivatives of 2 and 3-benzofurancarboxylates were synthesized under microwave-assisted conditions. Their in-vitro antimicrobial properties were assessed. Inhibition by the compounds of the growth of antibiotic-susceptible standards and clinically isolated strains of Gram-positive and Gram-negative bacteria, yeasts, and a human fungal pathogen was moderate to significant. Methyl 5-bromo-7-[2-(N,N-diethylamino)ethoxy]-6-methoxy-2-benzofurancarboxylate hydrochloride was identified as the most active compound (MIC 3?12 × 10?3 ?mol/cm3 against Gram-positive bacteria; MIC 9.4 × 10?2 ?mol/cm3 against Candida and Aspergillus brasiliensis). The molecular and crystal structures of 2-(N,N-diethylamino)ethyl 6-acetyl-5-hydroxy-2-methyl-3-benzofurancarboxylate were established by single-crystal X-ray diffraction. Graphical Abstract: . äMicrowave-assisted preparation and antimicrobial activity of O-alkylam(epmc).pdf DeepDyve Pubget Overpricing