{"id":11152,"date":"2022-11-21T05:00:35","date_gmt":"2022-11-20T21:00:35","guid":{"rendered":"https:\/\/www.pyrazoles-derivatives.com\/?p=11152"},"modified":"2022-11-21T05:00:35","modified_gmt":"2022-11-20T21:00:35","slug":"anderson-niall-a-s-team-published-research-in-organic-biomolecular-chemistry-in-14-cas-1025735-46-9","status":"publish","type":"post","link":"https:\/\/www.pyrazoles-derivatives.com\/?p=11152","title":{"rendered":"Anderson, Niall A.&#8217;s team published research in Organic &amp; Biomolecular Chemistry  in 14 | CAS: 1025735-46-9"},"content":{"rendered":"<p>Anderson, Niall A. published the artcile<b><i>Synthesis and determination of absolute configuration of a non-peptidic \u03b1<sub>v<\/sub>\u03b2<sub>6<\/sub> integrin antagonist for the treatment of idiopathic pulmonary fibrosis<\/i><\/b>,  <a href=\"https:\/\/www.ambeed.com\/products\/1025735-46-9.html\">Safety of 3-(3,5-Dimethyl-1H-pyrazol-1-yl)phenylboronic acid<\/a>,  the publication is  Organic &amp; Biomolecular Chemistry (2016), 14(25), 5992-6009, database is CAplus and MEDLINE.<\/p>\n<p>A diastereoselective synthesis of <strong>I<\/strong>, a potential therapeutic agent for the treatment of idiopathic pulmonary fibrosis, which is currently undergoing Phase I trials is reported. The key steps in the synthesis involved alkylation of 2-methylnaphthyridine with (R)-N-Boc-3-(iodomethyl)-pyrrolidine, and an asym. Rh-catalyzed addition of an arylboronic acid to a 4-(N-pyrrolidinyl)crotonate ester. The overall yield of the seven linear step synthesis is 8% and the product is obtained in &lt;99.5% ee proceeding with 80% de. The absolute configuration of <strong>I<\/strong> is established by an alternative asym. synthesis involving alkylation of an arylacetic acid using Evans oxazolidinone chem., acylation using the resulting 2-arylsuccinic acid, and reduction The absolute configuration of the benzylic asym. center is established as (S).<\/p>\n<p>Organic &amp; Biomolecular Chemistry published new progress about 1025735-46-9. 1025735-46-9 belongs to pyrazoles-derivatives, auxiliary class Pyrazole,Boronic acid and ester,Benzene,Boronic Acids, name is 3-(3,5-Dimethyl-1H-pyrazol-1-yl)phenylboronic acid, and the molecular formula is C11H13BN2O2, <a href=\"https:\/\/www.ambeed.com\/products\/1025735-46-9.html\">Safety of 3-(3,5-Dimethyl-1H-pyrazol-1-yl)phenylboronic acid<\/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>Organic &amp; Biomolecular Chemistry published new progress about 1025735-46-9. 1025735-46-9 belongs to pyrazoles-derivatives, auxiliary class Pyrazole,Boronic acid and ester,Benzene,Boronic Acids, name is 3-(3,5-Dimethyl-1H-pyrazol-1-yl)phenylboronic acid, and the molecular formula is C11H13BN2O2, <a href=\"https:\/\/www.ambeed.com\/products\/1025735-46-9.html\">Safety of 3-(3,5-Dimethyl-1H-pyrazol-1-yl)phenylboronic acid<\/a>.<\/p>\n","protected":false},"author":8,"featured_media":0,"comment_status":"closed","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[131],"tags":[716],"class_list":["post-11152","post","type-post","status-publish","format-standard","hentry","category-pyrazoles-derivatives","tag-m-w200-250"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v24.9 - https:\/\/yoast.com\/wordpress\/plugins\/seo\/ -->\n<title>Anderson, Niall A.&#039;s team published research in Organic &amp; Biomolecular Chemistry in 14 | CAS: 1025735-46-9 | pyrazoles-derivatives<\/title>\n<meta name=\"description\" content=\"Anderson, Niall A. published the artcileSynthesis and determination of absolute configuration of a non-peptidic \u03b1v\u03b26 integrin antagonist for the treatment of idiopathic pulmonary fibrosis, Safety of 3-(3,5-Dimethyl-1H-pyrazol-1-yl)phenylboronic acid, the publication is Organic &amp; 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