{"id":6998,"date":"2012-07-05T11:30:51","date_gmt":"2012-07-05T10:30:51","guid":{"rendered":"http:\/\/www.ch.imperial.ac.uk\/rzepa\/blog\/?p=6998"},"modified":"2012-07-05T11:30:51","modified_gmt":"2012-07-05T10:30:51","slug":"connections-in-chemistry-anti-malaria-drug-%e2%86%94-organocatalysis","status":"publish","type":"post","link":"https:\/\/www.rzepa.net\/blog\/?p=6998","title":{"rendered":"Connections in chemistry. Anti-malaria drug \u2194 organocatalysis."},"content":{"rendered":"<div class=\"kcite-section\" kcite-section-id=\"6998\">\n<p>Back in 1994, we published the crystal structure of the molecule below (X=H), a putative anti-malarial drug called <strong>halofantrine<\/strong>. Little did we realise that a whole area of organo catalysis based on a thiourea catalyst with a similar motif would emerge a little later. Here is how the two are connected.<\/p>\n<p style=\"text-align: center;\"><a href=\"http:\/\/www.ch.imperial.ac.uk\/rzepa\/blog\/wp-content\/uploads\/2012\/07\/halofantrine.svg\"><img loading=\"lazy\" decoding=\"async\" data-attachment-id=\"6999\" data-permalink=\"https:\/\/www.rzepa.net\/blog\/?attachment_id=6999\" data-orig-file=\"https:\/\/www.rzepa.net\/blog\/wp-content\/uploads\/2012\/07\/halofantrine.svg\" data-orig-size=\"\" data-comments-opened=\"1\" data-image-meta=\"[]\" data-image-title=\"halofantrine\" data-image-description=\"\" data-image-caption=\"\" data-medium-file=\"https:\/\/www.rzepa.net\/blog\/wp-content\/uploads\/2012\/07\/halofantrine.svg\" data-large-file=\"https:\/\/www.rzepa.net\/blog\/wp-content\/uploads\/2012\/07\/halofantrine.svg\" class=\"aligncenter  wp-image-6999\" title=\"halofantrine\" src=\"http:\/\/www.ch.imperial.ac.uk\/rzepa\/blog\/wp-content\/uploads\/2012\/07\/halofantrine.svg\" alt=\"\" width=\"169\" height=\"190\" \/><\/a><\/p>\n<p>In our <a href=\"http:\/\/dx.doi.org\/10.1039\/C39940001135\" target=\"_blank\">original article<\/a>\u00a0we described how our interest was sparked by observing the following chiral HPLC behaviour. The two enantiomers of compound <strong>2<\/strong>\u00a0(X=Y=Cl) separated nicely on the column. So did the compound where X=Cl, Y=H (<strong>4<\/strong>). However, when X=H,Y=Cl specifically (<strong>3<\/strong>), all chiral recognition on the column vanished! What was the reason?<\/p>\n<p style=\"text-align: center;\"><a href=\"https:\/\/i0.wp.com\/www.ch.imperial.ac.uk\/rzepa\/blog\/wp-content\/uploads\/2012\/07\/hplc.jpg\"><img data-recalc-dims=\"1\" loading=\"lazy\" decoding=\"async\" data-attachment-id=\"7000\" data-permalink=\"https:\/\/www.rzepa.net\/blog\/?attachment_id=7000\" data-orig-file=\"https:\/\/i0.wp.com\/www.rzepa.net\/blog\/wp-content\/uploads\/2012\/07\/hplc.jpg?fit=360%2C693&amp;ssl=1\" data-orig-size=\"360,693\" data-comments-opened=\"1\" data-image-meta=\"{&quot;aperture&quot;:&quot;0&quot;,&quot;credit&quot;:&quot;&quot;,&quot;camera&quot;:&quot;&quot;,&quot;caption&quot;:&quot;&quot;,&quot;created_timestamp&quot;:&quot;0&quot;,&quot;copyright&quot;:&quot;&quot;,&quot;focal_length&quot;:&quot;0&quot;,&quot;iso&quot;:&quot;0&quot;,&quot;shutter_speed&quot;:&quot;0&quot;,&quot;title&quot;:&quot;&quot;}\" data-image-title=\"hplc\" data-image-description=\"\" data-image-caption=\"\" data-medium-file=\"https:\/\/i0.wp.com\/www.rzepa.net\/blog\/wp-content\/uploads\/2012\/07\/hplc.jpg?fit=155%2C300&amp;ssl=1\" data-large-file=\"https:\/\/i0.wp.com\/www.rzepa.net\/blog\/wp-content\/uploads\/2012\/07\/hplc.jpg?fit=360%2C693&amp;ssl=1\" class=\"aligncenter  wp-image-7000\" title=\"hplc\" src=\"https:\/\/i0.wp.com\/www.ch.imperial.ac.uk\/rzepa\/blog\/wp-content\/uploads\/2012\/07\/hplc.jpg?resize=216%2C416\" alt=\"\" width=\"216\" height=\"416\" srcset=\"https:\/\/i0.wp.com\/www.rzepa.net\/blog\/wp-content\/uploads\/2012\/07\/hplc.jpg?w=360&amp;ssl=1 360w, https:\/\/i0.wp.com\/www.rzepa.net\/blog\/wp-content\/uploads\/2012\/07\/hplc.jpg?resize=155%2C300&amp;ssl=1 155w\" sizes=\"auto, (max-width: 216px) 100vw, 216px\" \/><\/a><\/p>\n<p>As it happens, we had recently acquired our <a href=\"http:\/\/www.ch.imperial.ac.uk\/rzepa\/blog\/?p=4647\">stereoscopic CAChe system<\/a>, and the structure was loaded into this. After a little while, we noticed that the compound formed a complementary dimer, glued together by C-H&#8230;O hydrogen bonds (magenta arrows below). When the H is replaced by Cl, this edge-on dimeric structure is completely destroyed, and is replaced by \u03c0-\u03c0 stacking instead.\u00a0<\/p>\n<div id=\"attachment_7001\" style=\"width: 410px\" class=\"wp-caption aligncenter\"><img data-recalc-dims=\"1\" decoding=\"async\" aria-describedby=\"caption-attachment-7001\" data-attachment-id=\"7001\" data-permalink=\"https:\/\/www.rzepa.net\/blog\/?attachment_id=7001\" data-orig-file=\"https:\/\/i0.wp.com\/www.rzepa.net\/blog\/wp-content\/uploads\/2012\/07\/halo-xray.jpg?fit=400%2C334&amp;ssl=1\" data-orig-size=\"400,334\" data-comments-opened=\"1\" data-image-meta=\"{&quot;aperture&quot;:&quot;0&quot;,&quot;credit&quot;:&quot;&quot;,&quot;camera&quot;:&quot;&quot;,&quot;caption&quot;:&quot;&quot;,&quot;created_timestamp&quot;:&quot;0&quot;,&quot;copyright&quot;:&quot;&quot;,&quot;focal_length&quot;:&quot;0&quot;,&quot;iso&quot;:&quot;0&quot;,&quot;shutter_speed&quot;:&quot;0&quot;,&quot;title&quot;:&quot;&quot;}\" data-image-title=\"halo-xray\" data-image-description=\"\" data-image-caption=\"&lt;p&gt;The dimeric structure of Halofantrine. Click for  3D&lt;\/p&gt;\n\" data-medium-file=\"https:\/\/i0.wp.com\/www.rzepa.net\/blog\/wp-content\/uploads\/2012\/07\/halo-xray.jpg?fit=300%2C250&amp;ssl=1\" data-large-file=\"https:\/\/i0.wp.com\/www.rzepa.net\/blog\/wp-content\/uploads\/2012\/07\/halo-xray.jpg?fit=400%2C334&amp;ssl=1\" class=\" wp-image-7001  \" title=\"halo-xray\" onclick=\"jmolInitialize('..\/Jmol\/');jmolSetAppletColor('white');jmolApplet([500,500],'load wp-content\/uploads\/2012\/07\/HEHXIB.cif; zoom 100;measure 33 137;measure 69 104;');\" src=\"https:\/\/i0.wp.com\/www.ch.imperial.ac.uk\/rzepa\/blog\/wp-content\/uploads\/2012\/07\/halo-xray.jpg?w=400\" alt=\"\"  srcset=\"https:\/\/i0.wp.com\/www.rzepa.net\/blog\/wp-content\/uploads\/2012\/07\/halo-xray.jpg?w=400&amp;ssl=1 400w, https:\/\/i0.wp.com\/www.rzepa.net\/blog\/wp-content\/uploads\/2012\/07\/halo-xray.jpg?resize=300%2C250&amp;ssl=1 300w\" sizes=\"(max-width: 400px) 100vw, 400px\" \/><p id=\"caption-attachment-7001\" class=\"wp-caption-text\">The dimeric structure of Halofantrine. Click for 3D<\/p><\/div>\n<p>The significance is that the hydrogen atom specifically antiperiplanar to the electron withdrawing CF<sub>3<\/sub> group was the one forming the C-H&#8230;O hydrogen bond (quite a short one as it happens, see 3D above). This despite 7-bonds separating the H-C from the CF<sub>3<\/sub> group. In the article,we speculated on how this effect of acidifying the hydrogen to encourage it to form a hydrogen bond might even be augmented. On historical note, we had made the article <a href=\"http:\/\/www.ch.ic.ac.uk\/rzepa\/RSC\/CC\/3_03989G.html\">available<\/a> using the then newly accessible World-Wide Web, providing <a href=\"http:\/\/www.ch.ic.ac.uk\/rzepa\/RSC\/CC\/3.mpg\">MPEG diagrams<\/a> corresponding to the structure above. It would be reasonable to claim that this is the very first article in chemistry to have been made so available, dating from mid 1994! If anyone can find an earlier example, do let me know! You might also note the difference between the MPEG movie and the presentation now available above.\u00a0<\/p>\n<p>In another part of the world a few years later, Peter Schreiner and his group were exploring organocatalysts based on thiourea (see\u00a0<a href=\"http:\/\/dx.doi.org\/10.1021\/jo201864e\">10.1021\/jo201864e<\/a> for a recent article) and in 2003 they had <a href=\"http:\/\/dx.doi.org\/10.1002\/chem.200390042\">discovered<\/a> remarkable catalytic properties for the system below.<\/p>\n<p style=\"text-align: center;\"><a href=\"http:\/\/www.ch.imperial.ac.uk\/rzepa\/blog\/wp-content\/uploads\/2012\/07\/thiourea.svg\"><img decoding=\"async\" data-attachment-id=\"7004\" data-permalink=\"https:\/\/www.rzepa.net\/blog\/?attachment_id=7004\" data-orig-file=\"https:\/\/www.rzepa.net\/blog\/wp-content\/uploads\/2012\/07\/thiourea.svg\" data-orig-size=\"\" data-comments-opened=\"1\" data-image-meta=\"[]\" data-image-title=\"thiourea\" data-image-description=\"\" data-image-caption=\"\" data-medium-file=\"https:\/\/www.rzepa.net\/blog\/wp-content\/uploads\/2012\/07\/thiourea.svg\" data-large-file=\"https:\/\/www.rzepa.net\/blog\/wp-content\/uploads\/2012\/07\/thiourea.svg\" class=\"aligncenter  wp-image-7004\" title=\"thiourea\" src=\"http:\/\/www.ch.imperial.ac.uk\/rzepa\/blog\/wp-content\/uploads\/2012\/07\/thiourea.svg\" alt=\"\" width=\"300\" \/><\/a><\/p>\n<p>As with us, they speculated that in addition to hydrogen bonds formed to substrates from the N-H groups, these could be augmented by rather weaker secondary interactions to the adjacent C-H bonds; certainly the presence of the CF<sub>3<\/sub> groups was the secret of these catalysts (now quite a family). It is tempting to conclude that both sets of observations are related by the same phenomenon!<\/p>\n<p>I end here by showing a <a href=\"http:\/\/hdl.handle.net\/10042\/20251\" target=\"_blank\">QTAIM analysis<\/a> of our halofantrine system (see <a href=\"http:\/\/www.ch.imperial.ac.uk\/rzepa\/blog\/?p=221\">similar analysis<\/a> for the Pirkle reagent). The key region indicated with magenta arrows above does indeed contain bond critical points (BCPs), with values of\u00a0\u03c1(r) ~ 0.045, which is near the top of the range experienced for hydrogen bonds of this type.<\/p>\n<div id=\"attachment_7016\" style=\"width: 410px\" class=\"wp-caption aligncenter\"><img data-recalc-dims=\"1\" loading=\"lazy\" decoding=\"async\" aria-describedby=\"caption-attachment-7016\" data-attachment-id=\"7016\" data-permalink=\"https:\/\/www.rzepa.net\/blog\/?attachment_id=7016\" data-orig-file=\"https:\/\/i0.wp.com\/www.rzepa.net\/blog\/wp-content\/uploads\/2012\/07\/halo-aim.jpg?fit=400%2C410&amp;ssl=1\" data-orig-size=\"400,410\" data-comments-opened=\"1\" data-image-meta=\"{&quot;aperture&quot;:&quot;0&quot;,&quot;credit&quot;:&quot;&quot;,&quot;camera&quot;:&quot;&quot;,&quot;caption&quot;:&quot;&quot;,&quot;created_timestamp&quot;:&quot;0&quot;,&quot;copyright&quot;:&quot;&quot;,&quot;focal_length&quot;:&quot;0&quot;,&quot;iso&quot;:&quot;0&quot;,&quot;shutter_speed&quot;:&quot;0&quot;,&quot;title&quot;:&quot;&quot;}\" data-image-title=\"halo-aim\" data-image-description=\"\" data-image-caption=\"&lt;p&gt;QTAIM analysis, showing three bond critical points. Click for  3D.&lt;\/p&gt;\n\" data-medium-file=\"https:\/\/i0.wp.com\/www.rzepa.net\/blog\/wp-content\/uploads\/2012\/07\/halo-aim.jpg?fit=292%2C300&amp;ssl=1\" data-large-file=\"https:\/\/i0.wp.com\/www.rzepa.net\/blog\/wp-content\/uploads\/2012\/07\/halo-aim.jpg?fit=400%2C410&amp;ssl=1\" class=\"size-full wp-image-7016\" title=\"halo-aim\" onclick=\"jmolInitialize('..\/Jmol\/');jmolSetAppletColor('white');jmolApplet([500,500],'load wp-content\/uploads\/2012\/07\/halo.mol; zoom 100;');\" src=\"https:\/\/i0.wp.com\/www.ch.imperial.ac.uk\/rzepa\/blog\/wp-content\/uploads\/2012\/07\/halo-aim.jpg?resize=400%2C410\" alt=\"\" width=\"400\" height=\"410\" srcset=\"https:\/\/i0.wp.com\/www.rzepa.net\/blog\/wp-content\/uploads\/2012\/07\/halo-aim.jpg?w=400&amp;ssl=1 400w, https:\/\/i0.wp.com\/www.rzepa.net\/blog\/wp-content\/uploads\/2012\/07\/halo-aim.jpg?resize=292%2C300&amp;ssl=1 292w\" sizes=\"auto, (max-width: 400px) 100vw, 400px\" \/><p id=\"caption-attachment-7016\" class=\"wp-caption-text\">QTAIM analysis, showing three bond critical points. Click for 3D.<\/p><\/div>\n<p>Connections like this probably permeate chemistry, and all too few of them are actually spotted.<\/p>\n<!-- kcite active, but no citations found -->\n<\/div> <!-- kcite-section 6998 -->","protected":false},"excerpt":{"rendered":"<p>Back in 1994, we published the crystal structure of the molecule below (X=H), a putative anti-malarial drug called halofantrine. Little did we realise that a whole area of organo catalysis based on a thiourea catalyst with a similar motif would emerge a little later. Here is how the two are connected. In our original article\u00a0we [&hellip;]<\/p>\n","protected":false},"author":1,"featured_media":0,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"jetpack_post_was_ever_published":false,"_jetpack_newsletter_access":"","_jetpack_dont_email_post_to_subs":false,"_jetpack_newsletter_tier_id":0,"_jetpack_memberships_contains_paywalled_content":false,"_jetpack_memberships_contains_paid_content":false,"footnotes":"","jetpack_publicize_message":"","jetpack_publicize_feature_enabled":true,"jetpack_social_post_already_shared":true,"jetpack_social_options":{"image_generator_settings":{"template":"highway","default_image_id":0,"font":"","enabled":false},"version":2}},"categories":[3,6],"tags":[1528,867,873,885],"class_list":["post-6998","post","type-post","status-publish","format-standard","hentry","category-chemical-it","category-interesting-chemistry","tag-historical","tag-mpeg","tag-peter-schreiner","tag-skolnik"],"jetpack_publicize_connections":[],"jetpack_featured_media_url":"","jetpack_sharing_enabled":true,"jetpack_shortlink":"https:\/\/wp.me\/p1gPyz-1OS","jetpack_likes_enabled":true,"_links":{"self":[{"href":"https:\/\/www.rzepa.net\/blog\/index.php?rest_route=\/wp\/v2\/posts\/6998","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/www.rzepa.net\/blog\/index.php?rest_route=\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/www.rzepa.net\/blog\/index.php?rest_route=\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/www.rzepa.net\/blog\/index.php?rest_route=\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/www.rzepa.net\/blog\/index.php?rest_route=%2Fwp%2Fv2%2Fcomments&post=6998"}],"version-history":[{"count":0,"href":"https:\/\/www.rzepa.net\/blog\/index.php?rest_route=\/wp\/v2\/posts\/6998\/revisions"}],"wp:attachment":[{"href":"https:\/\/www.rzepa.net\/blog\/index.php?rest_route=%2Fwp%2Fv2%2Fmedia&parent=6998"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.rzepa.net\/blog\/index.php?rest_route=%2Fwp%2Fv2%2Fcategories&post=6998"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.rzepa.net\/blog\/index.php?rest_route=%2Fwp%2Fv2%2Ftags&post=6998"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}