{"id":11115,"date":"2022-11-21T04:57:45","date_gmt":"2022-11-20T20:57:45","guid":{"rendered":"https:\/\/www.pyrazoles-derivatives.com\/?p=11115"},"modified":"2022-11-21T04:57:45","modified_gmt":"2022-11-20T20:57:45","slug":"sabate-alduy-catherines-team-published-research-in-bulletin-de-la-societe-chimique-de-france-in-cas-37599-34-1","status":"publish","type":"post","link":"https:\/\/www.pyrazoles-derivatives.com\/?p=11115","title":{"rendered":"Sabate-Alduy, Catherine&#8217;s team published research in Bulletin de la Societe Chimique de France  in  | CAS: 37599-34-1"},"content":{"rendered":"<p>Sabate-Alduy, Catherine published the artcile<b><i>1,3-Dipolar cycloaddition of diazomethane  Orientation of the addition of diazoalkanes to acetylenic compounds \u03b1-substituted with an alcohol or an ether group<\/i><\/b>,  <a href=\"https:\/\/www.ambeed.com\/products\/37599-34-1.html\">Product Details of C5H8N2O<\/a>,  the publication is  Bulletin de la Societe Chimique de France (1972), 2764-9, database is CAplus.<\/p>\n<p>The reaction of CH2N2 with acetylenic alcs. RR1CR2C\ue306CH (R and R1 = H, Me, Ph; (RR1) = (CH2)5; R2 = OH, NH2, OMe) was not stereospecific, giving 40-80% of the pyrazoles I and 20-60% of their isomers II (R3 = H). On the other hand the reaction with MeCHN2 was stereospecific, giving 80-100% I (R3 = Me). CH2N2 reacted with Me 3-(1-hydroxycyclohexyl)-propiolate to give 100% II [(RR1) = (CH2)5, R2 = OH, R3 = CO2Me , whereas with MeCHN2 a mixture of the isomers was obtained. Charge distribution calculations by the CNDO\/2 method confirm that the polarity of the acetylenic mol. determines the direction of the addition, rather than steric effects.<\/p>\n<p>Bulletin de la Societe Chimique de France published new progress about 37599-34-1. 37599-34-1 belongs to pyrazoles-derivatives, auxiliary class Pyrazole,Ether, name is 4-(methoxymethyl)-1H-pyrazole, and the molecular formula is C5H8N2O, <a href=\"https:\/\/www.ambeed.com\/products\/37599-34-1.html\">Product Details of C5H8N2O<\/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>Bulletin de la Societe Chimique de France published new progress about 37599-34-1. 37599-34-1 belongs to pyrazoles-derivatives, auxiliary class Pyrazole,Ether, name is 4-(methoxymethyl)-1H-pyrazole, and the molecular formula is C5H8N2O, <a href=\"https:\/\/www.ambeed.com\/products\/37599-34-1.html\">Product Details of C5H8N2O<\/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":[732],"class_list":["post-11115","post","type-post","status-publish","format-standard","hentry","category-pyrazoles-derivatives","tag-m-w100-150"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v24.9 - 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