{"id":11497,"date":"2022-11-28T04:25:17","date_gmt":"2022-11-27T20:25:17","guid":{"rendered":"https:\/\/www.pyrazoles-derivatives.com\/?p=11497"},"modified":"2022-11-28T04:25:17","modified_gmt":"2022-11-27T20:25:17","slug":"petzold-daniels-team-published-research-in-advanced-synthesis-catalysis-in-360-cas-930-36-9","status":"publish","type":"post","link":"https:\/\/www.pyrazoles-derivatives.com\/?p=11497","title":{"rendered":"Petzold, Daniel&#8217;s team published research in Advanced Synthesis &amp; Catalysis  in 360 | CAS: 930-36-9"},"content":{"rendered":"<p>Petzold, Daniel published the artcile<b><i>Photocatalytic Oxidative Bromination of Electron-Rich Arenes and Heteroarenes by Anthraquinone<\/i><\/b>,  <a href=\"https:\/\/www.ambeed.com\/products\/930-36-9.html\">Category: pyrazoles-derivatives<\/a>,  the publication is  Advanced Synthesis &amp; Catalysis (2018), 360(4), 626-630, database is CAplus.<\/p>\n<p>The estimated excited oxidation potential of sodium anthraquinone-2-sulfonate (SAS) increases from 1.8 V to \u223c2.3 V vs. SCE by protonation with Bronsted acids. This increased photooxidation power of protonated anthraquinone was used for the regio-selective oxidative bromination of electron rich (hetero)arenes and drugs in good yield. The mild reaction conditions are compatible with many functional groups, such as double and triple bonds, ketones, amides and amines, hydroxyl groups, carboxylic acids and carbamates. Mechanistic studies indicate the photooxidation of the arene followed by nucleophilic bromide addition as the likely pathway.<\/p>\n<p>Advanced Synthesis &amp; Catalysis published new progress about 930-36-9. 930-36-9 belongs to pyrazoles-derivatives, auxiliary class Pyrazole, name is 1-Methylpyrazole, and the molecular formula is C4H6N2, <a href=\"https:\/\/www.ambeed.com\/products\/930-36-9.html\">Category: pyrazoles-derivatives<\/a>.<\/p>\n<p>Referemce:<br \/><a href=\"https:\/\/en.wikipedia.org\/wiki\/Pyrazole\">https:\/\/en.wikipedia.org\/wiki\/Pyrazole<\/a>,<br \/><a href=\"Pyrazole - Wikipedia\">Pyrazoles &#8211; an overview | ScienceDirect Topics<\/a><\/p>\n","protected":false},"excerpt":{"rendered":"<p>Advanced Synthesis &amp; Catalysis published new progress about 930-36-9. 930-36-9 belongs to pyrazoles-derivatives, auxiliary class Pyrazole, name is 1-Methylpyrazole, and the molecular formula is C4H6N2, <a href=\"https:\/\/www.ambeed.com\/products\/930-36-9.html\">Category: pyrazoles-derivatives<\/a>.<\/p>\n","protected":false},"author":8,"featured_media":0,"comment_status":"closed","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[245,131],"tags":[784],"class_list":["post-11497","post","type-post","status-publish","format-standard","hentry","category-930-36-9","category-pyrazoles-derivatives","tag-m-w50-100"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v24.9 - https:\/\/yoast.com\/wordpress\/plugins\/seo\/ -->\n<title>Petzold, Daniel&#039;s team published research in Advanced Synthesis &amp; 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