Green synthesis and antifungal activities of novel 3‐(trifluoromethyl)‐4,5‐dihydro‐1H‐furo[2,3‐c]pyrazole derivatives
Trifluoromethylated molecules, as well as pyrazol‐3‐one derivatives, are found in a wide range of biologically active compounds. An highly facile, green and mild access to substituted 3‐(trifluoromethyl)‐4,5‐dihydro‐1H‐furo[2,3‐c]pyrazole derivatives by the cascade [3 + 2] Michael/Alkylation of unsa...
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Veröffentlicht in: | Journal of heterocyclic chemistry 2020-07, Vol.57 (7), p.2904-2910 |
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container_title | Journal of heterocyclic chemistry |
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creator | Tan, Fangshun Su, Shennan Liu, Zhenzhong |
description | Trifluoromethylated molecules, as well as pyrazol‐3‐one derivatives, are found in a wide range of biologically active compounds. An highly facile, green and mild access to substituted 3‐(trifluoromethyl)‐4,5‐dihydro‐1H‐furo[2,3‐c]pyrazole derivatives by the cascade [3 + 2] Michael/Alkylation of unsaturated pyrazolones with α‐bromomalonate has been developed. The reactions can be performed in a easily available and environmentally benign solvent, and the substituted 3‐(trifluoromethyl)‐4,5‐dihydro‐1H‐furo[2,3‐c]pyrazole derivatives can be obtained in good to excellent yields by a simple purification step. The antifungal activities of these functional pyrazole derivatives were also evaluated and they showed high antifungal activity against Alternaria solani. |
doi_str_mv | 10.1002/jhet.3998 |
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An highly facile, green and mild access to substituted 3‐(trifluoromethyl)‐4,5‐dihydro‐1H‐furo[2,3‐c]pyrazole derivatives by the cascade [3 + 2] Michael/Alkylation of unsaturated pyrazolones with α‐bromomalonate has been developed. The reactions can be performed in a easily available and environmentally benign solvent, and the substituted 3‐(trifluoromethyl)‐4,5‐dihydro‐1H‐furo[2,3‐c]pyrazole derivatives can be obtained in good to excellent yields by a simple purification step. The antifungal activities of these functional pyrazole derivatives were also evaluated and they showed high antifungal activity against Alternaria solani.</description><identifier>ISSN: 0022-152X</identifier><identifier>EISSN: 1943-5193</identifier><identifier>DOI: 10.1002/jhet.3998</identifier><language>eng</language><publisher>Chichester, UK: John Wiley & Sons, Inc</publisher><ispartof>Journal of heterocyclic chemistry, 2020-07, Vol.57 (7), p.2904-2910</ispartof><rights>2020 Wiley Periodicals LLC</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fjhet.3998$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fjhet.3998$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids></links><search><creatorcontrib>Tan, Fangshun</creatorcontrib><creatorcontrib>Su, Shennan</creatorcontrib><creatorcontrib>Liu, Zhenzhong</creatorcontrib><title>Green synthesis and antifungal activities of novel 3‐(trifluoromethyl)‐4,5‐dihydro‐1H‐furo[2,3‐c]pyrazole derivatives</title><title>Journal of heterocyclic chemistry</title><description>Trifluoromethylated molecules, as well as pyrazol‐3‐one derivatives, are found in a wide range of biologically active compounds. 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title | Green synthesis and antifungal activities of novel 3‐(trifluoromethyl)‐4,5‐dihydro‐1H‐furo[2,3‐c]pyrazole derivatives |
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