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10.3762/bjoc.13.169 http://scihub22266oqcxt.onion/10.3762/bjoc.13.169 C5588455!5588455!28904618     free     free     free Warning: imagejpeg(C:\Inetpub\vhosts\kidney.de\httpdocs\phplern\28904618.jpg): Failed to open stream: No such file or directory in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 117       Beilstein+J+Org+Chem 2017 ; 13 (ä): 1745-52 Nephropedia Template TP {{tp|p=28904618|t=2017. Mechanochemical N-alkylation of imides |pdf=|usr=}}{{28904618}} gab.com Text Mechanochemical N-alkylation of imides JO: Beilstein J Org Chem http://www.kidney.de/pget.php?&tw=1&pmid=28904618 #FOAvip The mechanochemical N-alkylation of imide derivatives was studied. Reactions under solvent-free conditions in a ball mill gave good yields and could be put in place of the classical solution conditions. The method is general and can be applied to various imides and alkyl halides. Phthalimides prepared under ball milling conditions were used in a mechanochemical Gabriel synthesis of amines by their reaction with 1,2-diaminoethane. Twit Text FOAVip Mechanochemical N-alkylation of imides ????Beilstein J Org Chem http://www.kidney.de/pget.php?&tw=1&pmid=28904618 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=28904618 #FOAvip English Wikipedia <ref>{{Cite pmid|28904618}}</ref> Mechanochemical N-alkylation of imides #MMPMID28904618 Bri? A; ?ud M; Margeti? D Beilstein J Org Chem 2017[]; 13 (ä): 1745-52 PMID28904618show ga The mechanochemical N-alkylation of imide derivatives was studied. Reactions under solvent-free conditions in a ball mill gave good yields and could be put in place of the classical solution conditions. The method is general and can be applied to various imides and alkyl halides. Phthalimides prepared under ball milling conditions were used in a mechanochemical Gabriel synthesis of amines by their reaction with 1,2-diaminoethane. äMechanochemical N-alkylation of imides (epmc).pdf DeepDyve Pubget Overpricing