{"id":7242,"date":"2021-10-28T02:06:17","date_gmt":"2021-10-27T18:06:17","guid":{"rendered":"https:\/\/www.pyrazoles-derivatives.com\/?p=7242"},"modified":"2021-10-28T02:06:17","modified_gmt":"2021-10-27T18:06:17","slug":"simple-exploration-of-86-92-0","status":"publish","type":"post","link":"https:\/\/www.pyrazoles-derivatives.com\/?p=7242","title":{"rendered":"Simple exploration of 86-92-0"},"content":{"rendered":"<p><a href=\"https:\/\/www.ambeed.com\/products\/86-92-0.html\">Recommanded Product: 86-92-0<\/a>. Lu, H; Zhang, HX; Tan, CY; Liu, JY; Wei, H; Xu, PF in [Lu, Hong; Zhang, Huan-Xin; Tan, Chang-Yin; Liu, Jin-Yu; Xu, Peng-Fei] Lanzhou Univ, Sch Chem &#038; Chem Engn, State Key Lab Appl Organ Chem, Lanzhou 730000, Gansu, Peoples R China; [Lu, Hong; Wei, Hao] Northwest Univ, Coll Chem &#038; Mat Sci, Natl Demonstrat Ctr Expt Chem Educ, Key Lab Synthet &#038; Nat Funct Mol Chem,Minist Educ, Xian 710127, Shaanxi, Peoples R China published One-Pot Asymmetric Synthesis of Spiropyrazolone-Linked Cyclopropanes and Benzofurans through a General Michael Addition\/Chlorination\/Nucleophilic Substitution Sequence in 2019, Cited 45. The Name is 3-Methyl-1-p-tolyl-5-pyrazolone. Through research, I have a further understanding and discovery of 86-92-0.<\/p>\n<p>A sequential and general strategy has been successfully developed for the synthesis of spiropyrazolone scaffolds. This intriguing transformation of the asymmetric multicomponent catalysis process was realized with the combination of Michael addition\/chlorination\/nucleophilic substitution in a one-pot sequence, giving rise to a series of spiropyrazolones with fully substituted cyclopropanes and spiro-dihydrobenzofurans containing continuous stereogenic centers in good yields with excellent stereoselectivities.<\/p>\n<p>About 3-Methyl-1-p-tolyl-5-pyrazolone, If you have any questions, you can contact Lu, H; Zhang, HX; Tan, CY; Liu, JY; Wei, H; Xu, PF or concate me.. <a href=\"https:\/\/www.ambeed.com\/products\/86-92-0.html\">Recommanded Product: 86-92-0<\/a><\/p>\n<p>Reference:<br \/><a href=\"https:\/\/doi.org\/10.1016\/j.tet.2019.130916\">Article; Zhang, Yong; Nie, Long-Jun; Luo, Liang; Mao, Jia-Xin; Liu, Jin-Xiang; Xu, Guo-Hai; Chen, Deliang; Luo, Hai-Qing; Tetrahedron; vol. 76; 7; (2020);<\/a>,<br \/><a href=\"https:\/\/en.wikipedia.org\/wiki\/Pyrazole\">Pyrazole &#8211; Wikipedia<\/a>,<br \/><a href=\"https:\/\/www.sciencedirect.com\/topics\/chemistry\/pyrazoles\">Pyrazoles &#8211; an overview | ScienceDirect Topics<\/p>\n","protected":false},"excerpt":{"rendered":"<p>About 3-Methyl-1-p-tolyl-5-pyrazolone, If you have any questions, you can contact Lu, H; Zhang, HX; Tan, CY; Liu, JY; Wei, H; Xu, PF or concate me.. <a href=\"https:\/\/www.ambeed.com\/products\/86-92-0.html\">Recommanded Product: 86-92-0<\/a><\/p>\n","protected":false},"author":8,"featured_media":0,"comment_status":"closed","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[675,131],"tags":[717],"class_list":["post-7242","post","type-post","status-publish","format-standard","hentry","category-86-92-0","category-pyrazoles-derivatives","tag-m-w150-200"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v24.9 - https:\/\/yoast.com\/wordpress\/plugins\/seo\/ -->\n<title>Simple exploration of 86-92-0 | pyrazoles-derivatives<\/title>\n<meta name=\"description\" content=\"Recommanded Product: 86-92-0. Lu, H; Zhang, HX; Tan, CY; Liu, JY; Wei, H; Xu, PF in [Lu, Hong; Zhang, Huan-Xin; Tan, Chang-Yin; Liu, Jin-Yu; Xu, Peng-Fei] Lanzhou Univ, Sch Chem &amp; Chem Engn, State Key Lab Appl Organ Chem, Lanzhou 730000, Gansu, Peoples R China; [Lu, Hong; Wei, Hao] Northwest Univ, Coll Chem &amp; Mat Sci, Natl Demonstrat Ctr Expt Chem Educ, Key Lab Synthet &amp; Nat Funct Mol Chem,Minist Educ, Xian 710127, Shaanxi, Peoples R China published One-Pot Asymmetric Synthesis of Spiropyrazolone-Linked Cyclopropanes and Benzofurans through a General Michael Addition\/Chlorination\/Nucleophilic Substitution Sequence in 2019, Cited 45. The Name is 3-Methyl-1-p-tolyl-5-pyrazolone. Through research, I have a further understanding and discovery of 86-92-0.\" \/>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/www.pyrazoles-derivatives.com\/?p=7242\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Simple exploration of 86-92-0 | pyrazoles-derivatives\" \/>\n<meta property=\"og:description\" content=\"Recommanded Product: 86-92-0. Lu, H; Zhang, HX; Tan, CY; Liu, JY; Wei, H; Xu, PF in [Lu, Hong; Zhang, Huan-Xin; Tan, Chang-Yin; Liu, Jin-Yu; Xu, Peng-Fei] Lanzhou Univ, Sch Chem &amp; Chem Engn, State Key Lab Appl Organ Chem, Lanzhou 730000, Gansu, Peoples R China; [Lu, Hong; Wei, Hao] Northwest Univ, Coll Chem &amp; Mat Sci, Natl Demonstrat Ctr Expt Chem Educ, Key Lab Synthet &amp; Nat Funct Mol Chem,Minist Educ, Xian 710127, Shaanxi, Peoples R China published One-Pot Asymmetric Synthesis of Spiropyrazolone-Linked Cyclopropanes and Benzofurans through a General Michael Addition\/Chlorination\/Nucleophilic Substitution Sequence in 2019, Cited 45. The Name is 3-Methyl-1-p-tolyl-5-pyrazolone. Through research, I have a further understanding and discovery of 86-92-0.\" \/>\n<meta property=\"og:url\" content=\"https:\/\/www.pyrazoles-derivatives.com\/?p=7242\" \/>\n<meta property=\"og:site_name\" content=\"pyrazoles-derivatives\" \/>\n<meta property=\"article:published_time\" content=\"2021-10-27T18:06:17+00:00\" \/>\n<meta name=\"author\" content=\"Jessica.F\" \/>\n<meta name=\"twitter:card\" content=\"summary_large_image\" \/>\n<meta name=\"twitter:label1\" content=\"Written by\" \/>\n\t<meta name=\"twitter:data1\" content=\"Jessica.F\" \/>\n\t<meta name=\"twitter:label2\" content=\"Est. reading time\" \/>\n\t<meta name=\"twitter:data2\" content=\"1 minute\" \/>\n<script type=\"application\/ld+json\" class=\"yoast-schema-graph\">{\"@context\":\"https:\/\/schema.org\",\"@graph\":[{\"@type\":\"WebPage\",\"@id\":\"https:\/\/www.pyrazoles-derivatives.com\/?p=7242\",\"url\":\"https:\/\/www.pyrazoles-derivatives.com\/?p=7242\",\"name\":\"Simple exploration of 86-92-0 | pyrazoles-derivatives\",\"isPartOf\":{\"@id\":\"https:\/\/www.pyrazoles-derivatives.com\/#website\"},\"datePublished\":\"2021-10-27T18:06:17+00:00\",\"author\":{\"@id\":\"https:\/\/www.pyrazoles-derivatives.com\/#\/schema\/person\/d9a9f27bed675392c6f363a01ffd49f1\"},\"description\":\"Recommanded Product: 86-92-0. Lu, H; Zhang, HX; Tan, CY; Liu, JY; Wei, H; Xu, PF in [Lu, Hong; Zhang, Huan-Xin; Tan, Chang-Yin; Liu, Jin-Yu; Xu, Peng-Fei] Lanzhou Univ, Sch Chem & Chem Engn, State Key Lab Appl Organ Chem, Lanzhou 730000, Gansu, Peoples R China; [Lu, Hong; Wei, Hao] Northwest Univ, Coll Chem & Mat Sci, Natl Demonstrat Ctr Expt Chem Educ, Key Lab Synthet & Nat Funct Mol Chem,Minist Educ, Xian 710127, Shaanxi, Peoples R China published One-Pot Asymmetric Synthesis of Spiropyrazolone-Linked Cyclopropanes and Benzofurans through a General Michael Addition\/Chlorination\/Nucleophilic Substitution Sequence in 2019, Cited 45. The Name is 3-Methyl-1-p-tolyl-5-pyrazolone. 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Lu, H; Zhang, HX; Tan, CY; Liu, JY; Wei, H; Xu, PF in [Lu, Hong; Zhang, Huan-Xin; Tan, Chang-Yin; Liu, Jin-Yu; Xu, Peng-Fei] Lanzhou Univ, Sch Chem & Chem Engn, State Key Lab Appl Organ Chem, Lanzhou 730000, Gansu, Peoples R China; [Lu, Hong; Wei, Hao] Northwest Univ, Coll Chem & Mat Sci, Natl Demonstrat Ctr Expt Chem Educ, Key Lab Synthet & Nat Funct Mol Chem,Minist Educ, Xian 710127, Shaanxi, Peoples R China published One-Pot Asymmetric Synthesis of Spiropyrazolone-Linked Cyclopropanes and Benzofurans through a General Michael Addition\/Chlorination\/Nucleophilic Substitution Sequence in 2019, Cited 45. The Name is 3-Methyl-1-p-tolyl-5-pyrazolone. 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Lu, H; Zhang, HX; Tan, CY; Liu, JY; Wei, H; Xu, PF in [Lu, Hong; Zhang, Huan-Xin; Tan, Chang-Yin; Liu, Jin-Yu; Xu, Peng-Fei] Lanzhou Univ, Sch Chem & Chem Engn, State Key Lab Appl Organ Chem, Lanzhou 730000, Gansu, Peoples R China; [Lu, Hong; Wei, Hao] Northwest Univ, Coll Chem & Mat Sci, Natl Demonstrat Ctr Expt Chem Educ, Key Lab Synthet & Nat Funct Mol Chem,Minist Educ, Xian 710127, Shaanxi, Peoples R China published One-Pot Asymmetric Synthesis of Spiropyrazolone-Linked Cyclopropanes and Benzofurans through a General Michael Addition\/Chlorination\/Nucleophilic Substitution Sequence in 2019, Cited 45. The Name is 3-Methyl-1-p-tolyl-5-pyrazolone. 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Lu, H; Zhang, HX; Tan, CY; Liu, JY; Wei, H; Xu, PF in [Lu, Hong; Zhang, Huan-Xin; Tan, Chang-Yin; Liu, Jin-Yu; Xu, Peng-Fei] Lanzhou Univ, Sch Chem & Chem Engn, State Key Lab Appl Organ Chem, Lanzhou 730000, Gansu, Peoples R China; [Lu, Hong; Wei, Hao] Northwest Univ, Coll Chem & Mat Sci, Natl Demonstrat Ctr Expt Chem Educ, Key Lab Synthet & Nat Funct Mol Chem,Minist Educ, Xian 710127, Shaanxi, Peoples R China published One-Pot Asymmetric Synthesis of Spiropyrazolone-Linked Cyclopropanes and Benzofurans through a General Michael Addition\/Chlorination\/Nucleophilic Substitution Sequence in 2019, Cited 45. The Name is 3-Methyl-1-p-tolyl-5-pyrazolone. 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