{"id":672,"date":"2011-03-01T13:27:56","date_gmt":"2011-03-01T18:27:56","guid":{"rendered":"http:\/\/scholarblogs.emory.edu\/davieslab\/?p=672"},"modified":"2018-07-12T14:01:41","modified_gmt":"2018-07-12T19:01:41","slug":"214-guiding-principles-for-site-selective-and-stereoselective-intermolecular-c-h-functionalization-by-donoracceptor-rhodium-carbenes","status":"publish","type":"post","link":"https:\/\/scholarblogs.emory.edu\/davieslab\/2011\/03\/01\/214-guiding-principles-for-site-selective-and-stereoselective-intermolecular-c-h-functionalization-by-donoracceptor-rhodium-carbenes\/","title":{"rendered":"214. Guiding principles for site selective and stereoselective intermolecular C\u2013H functionalization by donor\/acceptor rhodium carbenes"},"content":{"rendered":"<p>Authors:\u00a0Huw M. L. Davies and Daniel Morton<\/p>\n<p><em>Chem. Soc. Rev.,\u00a0<\/em><\/p>\n<p><strong>2011<\/strong>,\u00a0<em>40, <\/em>1857-1869<\/p>\n<p><a href=\"http:\/\/scholarblogs.emory.edu\/davieslab\/files\/2013\/12\/030.gif\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone size-medium wp-image-673 aligncenter\" alt=\"030\" src=\"http:\/\/scholarblogs.emory.edu\/davieslab\/files\/2013\/12\/030-300x146.gif\" width=\"300\" height=\"146\" \/><\/a><\/p>\n<p><!--more--><\/p>\n<p>This tutorial review presents a description of the controlling elements of intermolecular C\u2013H functionalization by means of C\u2013H insertion by donor\/acceptor rhodium carbenes. These rhodium carbenes, readily derived from the combination of diazo compounds with dirhodium(II) catalysts, are sufficiently reactive to undergo a wide range of C\u2013H insertions. They are also capable of highly selective reactions, controlled by a combination of steric and electronic factors. An overview of the structural factors that influence site selectivity will be given, followed by a description of the exceptional diastereo- and enantioselectivity that can be achieved. Several examples will be shown of how this methodology can be applied to streamline the synthesis of natural products and pharmaceutical targets.<\/p>\n<p><a href=\"http:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2011\/cs\/c0cs00217h#!divAbstract\" target=\"_blank\">Read More<\/a><\/p>\n","protected":false},"excerpt":{"rendered":"<p>Authors:\u00a0Huw M. L. Davies and Daniel Morton Chem. Soc. Rev.,\u00a0 2011,\u00a040, 1857-1869<\/p>\n","protected":false},"author":5441,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"ngg_post_thumbnail":0,"footnotes":""},"categories":[8],"tags":[16,3,38,7,90,14,30],"class_list":["post-672","post","type-post","status-publish","format-standard","hentry","category-publications","tag-carbenoid","tag-c-h-functionalization","tag-donoracceptor","tag-dosp","tag-ptad","tag-rhodiumii","tag-vinyl-carbenoid"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.3 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>214. 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