<?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%">Biju, Akkattu T.</style></author><author><style face="normal" font="default" size="100%">Hirano, Keiichi</style></author><author><style face="normal" font="default" size="100%">Frohlich, Roland</style></author><author><style face="normal" font="default" size="100%">Glorius, Frank</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Switching the electron-donor properties of n-heterocyclic carbenes by a facile deprotonation strategy</style></title><secondary-title><style face="normal" font="default" size="100%">Chemistry an Asian Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">carbenes; electronic properties; enolates; heterocycles; ligand design</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2009</style></year><pub-dates><date><style  face="normal" font="default" size="100%">DEC</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">9</style></volume><pages><style face="normal" font="default" size="100%">1786–1789</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;Flip the switch! The facile and distinct variation of the electronic properties of an N-heterocyclic carbene (NHC) ligand is reported. In this process, a simple deprotonation/protonation strategy can render the NHC to be an electron-poor or an electron-rich NHC ligand: one ligand, two electronic natures.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">12</style></issue><custom3><style face="normal" font="default" size="100%">Foreign</style></custom3><custom4><style face="normal" font="default" size="100%">4.188</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%">Loewer, Yvonne</style></author><author><style face="normal" font="default" size="100%">Weiss, Christine</style></author><author><style face="normal" font="default" size="100%">Biju, Akkattu T.</style></author><author><style face="normal" font="default" size="100%">Frohlich, Roland</style></author><author><style face="normal" font="default" size="100%">Glorius, Frank</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Synthesis and application of a chiral diborate</style></title><secondary-title><style face="normal" font="default" size="100%">Journal of Organic Chemistry</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2011</style></year><pub-dates><date><style  face="normal" font="default" size="100%">MAR</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">76</style></volume><pages><style face="normal" font="default" size="100%">2324–2327</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 chiral diborate with different counterions is reported whose structure was unambiguously confirmed by X-ray analysis. This chiral dianion was used in the resolution of trans-1,2-diamines and also as a chiral shift reagent for NMR analysis of triphenylphosphonium salts.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">7</style></issue><custom2><style face="normal" font="default" size="100%">&lt;p&gt;Council of Scientific &amp;amp; Industrial Research (CSIR) - India&lt;/p&gt;</style></custom2><custom3><style face="normal" font="default" size="100%">Foreign</style></custom3><custom4><style face="normal" font="default" size="100%">4.45
</style></custom4></record></records></xml>