<?xml version="1.0" encoding="UTF-8"?><xml><records><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Midya, Siba P.</style></author><author><style face="normal" font="default" size="100%">Mondal, Akash</style></author><author><style face="normal" font="default" size="100%">Begum, Ayesha</style></author><author><style face="normal" font="default" size="100%">Balaraman, Ekambaram</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Simple cobalt(II) chloride catalyzed N-alkylation of amines with alcohols</style></title><secondary-title><style face="normal" font="default" size="100%">Synthesis-Stuttgart </style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">(Hetero)Aromatic Amines</style></keyword><keyword><style  face="normal" font="default" size="100%">Alcohols</style></keyword><keyword><style  face="normal" font="default" size="100%">Amination</style></keyword><keyword><style  face="normal" font="default" size="100%">amines</style></keyword><keyword><style  face="normal" font="default" size="100%">Anilines</style></keyword><keyword><style  face="normal" font="default" size="100%">Aromatic-amines</style></keyword><keyword><style  face="normal" font="default" size="100%">Cobalt Catalysis</style></keyword><keyword><style  face="normal" font="default" size="100%">Dehydrogenation Borrowing Hydrogen</style></keyword><keyword><style  face="normal" font="default" size="100%">Efficient Catalysts</style></keyword><keyword><style  face="normal" font="default" size="100%">Hydrogen Autotransfer</style></keyword><keyword><style  face="normal" font="default" size="100%">Iridium</style></keyword><keyword><style  face="normal" font="default" size="100%">N-alkylation</style></keyword><keyword><style  face="normal" font="default" size="100%">Pincer-complex</style></keyword><keyword><style  face="normal" font="default" size="100%">Secondary Alcohols</style></keyword><keyword><style  face="normal" font="default" size="100%">Selective Alkylation</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2017</style></year><pub-dates><date><style  face="normal" font="default" size="100%">SEP</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">49</style></volume><pages><style face="normal" font="default" size="100%">3957-3961</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;&lt;span style=&quot;color: rgb(51, 51, 51); font-family: arial, helvetica, sans-serif; font-size: 13px; background-color: rgb(248, 248, 248);&quot;&gt;A facile cobalt-catalyzed N-alkylation of amines with alcohols using inexpensive, commercially available CoCl2 center dot 6H(2)O is reported. Employing this readily available cobalt catalyst, a variety of amines with wide functional group tolerance were selectively alkylated under benign conditions.&lt;/span&gt;&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">17</style></issue><work-type><style face="normal" font="default" size="100%">Journal Article</style></work-type><custom3><style face="normal" font="default" size="100%">&lt;p&gt;Foreign&lt;/p&gt;</style></custom3><custom4><style face="normal" font="default" size="100%">&lt;p&gt;2.652&lt;/p&gt;</style></custom4><section><style face="normal" font="default" size="100%">3957-3961</style></section></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Landge, Vinod G.</style></author><author><style face="normal" font="default" size="100%">Mondal, Akash</style></author><author><style face="normal" font="default" size="100%">Kumar, Vinit</style></author><author><style face="normal" font="default" size="100%">Nandakumar, Avanashiappn</style></author><author><style face="normal" font="default" size="100%">Balaraman, Ekambaram</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Manganese catalyzed N-alkylation of anilines with alcohols: ligand enabled selectivity</style></title><secondary-title><style face="normal" font="default" size="100%">Organic and biomolecular chemistry </style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2018</style></year><pub-dates><date><style  face="normal" font="default" size="100%">NOV</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">16</style></volume><pages><style face="normal" font="default" size="100%">8175-8180</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">Ligand enabled Earth-abundant manganese catalyzed N-alkylation of amines with alcohols via a hydrogen auto-transfer strategy is reported. The choice of the ligand plays a significant role in the alcohol reactivity (aliphatic or aromatic) toward N-alkylation reactions.</style></abstract><issue><style face="normal" font="default" size="100%">43</style></issue><work-type><style face="normal" font="default" size="100%">Article </style></work-type><custom3><style face="normal" font="default" size="100%">Foreign</style></custom3><custom4><style face="normal" font="default" size="100%">3.423</style></custom4></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Mondal, Akash</style></author><author><style face="normal" font="default" size="100%">Subaramanian, Murugan</style></author><author><style face="normal" font="default" size="100%">Avanashiappan, Nandakumar</style></author><author><style face="normal" font="default" size="100%">Balaraman, Kambaram</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Manganese-catalyzed direct conversion of ester to amide with liberation of H 2</style></title><secondary-title><style face="normal" font="default" size="100%">Organic Letters</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2018</style></year><pub-dates><date><style  face="normal" font="default" size="100%">JUN</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">20</style></volume><pages><style face="normal" font="default" size="100%">3381-3384</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;A simple and efficient Mn-catalyzed acylation of amines is achieved using both acyl and alkoxy functions of unactivated esters with the liberation of molecular hydrogen as a sole byproduct. The present protocol provides an atom-economical and sustainable route for the synthesis of amides from esters by employing an earth-abundant manganese salt and inexpensive phosphine-free tridentate ligand.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">11</style></issue><work-type><style face="normal" font="default" size="100%">Article</style></work-type><custom3><style face="normal" font="default" size="100%">&lt;p&gt;Foreign&lt;/p&gt;</style></custom3><custom4><style face="normal" font="default" size="100%">&lt;p&gt;6.579&lt;/p&gt;</style></custom4></record></records></xml>