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Water-mediated and promoted eco-friendly one-pot synthesis of azaarene substituted isoxazolesElectronic supplementary information (ESI) available. See DOI: 10.1039/c7nj01165b
An efficient and green approach for the sp 3 C-H bond functionalization of 2-methyl azaarenes to 3-methyl-4-nitro-5-styrylisoxazoles in water has been described. Nitrostyrylisoxazoles were proven to be good C&z.dbd;C electrophilic acceptors for the construction of various azaarene-containing Mic...
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creator | Nagaraju, Dharavath Rajanarendar, Eligeti Praveen Kumar, Pittala Nagi Reddy, Modugu |
description | An efficient and green approach for the sp
3
C-H bond functionalization of 2-methyl azaarenes to 3-methyl-4-nitro-5-styrylisoxazoles in water has been described. Nitrostyrylisoxazoles were proven to be good C&z.dbd;C electrophilic acceptors for the construction of various azaarene-containing Michael addition products. This method provides an efficient and environmentally benign method for the one-pot synthesis of biologically important azaarene-substituted isoxazole derivatives in good yields. The important aspects of the present methodology are the use of non-toxic solvent, that it is catalyst free, the ease of purification and the large substrate scope.
An efficient and green approach for the sp
3
C-H bond functionalization of 2-methyl azaarenes to 3-methyl-4-nitro-5-styrylisoxazoles in water has been described. |
doi_str_mv | 10.1039/c7nj01165b |
format | article |
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3
C-H bond functionalization of 2-methyl azaarenes to 3-methyl-4-nitro-5-styrylisoxazoles in water has been described. Nitrostyrylisoxazoles were proven to be good C&z.dbd;C electrophilic acceptors for the construction of various azaarene-containing Michael addition products. This method provides an efficient and environmentally benign method for the one-pot synthesis of biologically important azaarene-substituted isoxazole derivatives in good yields. The important aspects of the present methodology are the use of non-toxic solvent, that it is catalyst free, the ease of purification and the large substrate scope.
An efficient and green approach for the sp
3
C-H bond functionalization of 2-methyl azaarenes to 3-methyl-4-nitro-5-styrylisoxazoles in water has been described.</description><identifier>ISSN: 1144-0546</identifier><identifier>EISSN: 1369-9261</identifier><identifier>DOI: 10.1039/c7nj01165b</identifier><language>eng</language><creationdate>2017-06</creationdate><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids></links><search><creatorcontrib>Nagaraju, Dharavath</creatorcontrib><creatorcontrib>Rajanarendar, Eligeti</creatorcontrib><creatorcontrib>Praveen Kumar, Pittala</creatorcontrib><creatorcontrib>Nagi Reddy, Modugu</creatorcontrib><title>Water-mediated and promoted eco-friendly one-pot synthesis of azaarene substituted isoxazolesElectronic supplementary information (ESI) available. See DOI: 10.1039/c7nj01165b</title><description>An efficient and green approach for the sp
3
C-H bond functionalization of 2-methyl azaarenes to 3-methyl-4-nitro-5-styrylisoxazoles in water has been described. Nitrostyrylisoxazoles were proven to be good C&z.dbd;C electrophilic acceptors for the construction of various azaarene-containing Michael addition products. This method provides an efficient and environmentally benign method for the one-pot synthesis of biologically important azaarene-substituted isoxazole derivatives in good yields. The important aspects of the present methodology are the use of non-toxic solvent, that it is catalyst free, the ease of purification and the large substrate scope.
An efficient and green approach for the sp
3
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3
C-H bond functionalization of 2-methyl azaarenes to 3-methyl-4-nitro-5-styrylisoxazoles in water has been described. Nitrostyrylisoxazoles were proven to be good C&z.dbd;C electrophilic acceptors for the construction of various azaarene-containing Michael addition products. This method provides an efficient and environmentally benign method for the one-pot synthesis of biologically important azaarene-substituted isoxazole derivatives in good yields. The important aspects of the present methodology are the use of non-toxic solvent, that it is catalyst free, the ease of purification and the large substrate scope.
An efficient and green approach for the sp
3
C-H bond functionalization of 2-methyl azaarenes to 3-methyl-4-nitro-5-styrylisoxazoles in water has been described.</abstract><doi>10.1039/c7nj01165b</doi><tpages>5</tpages></addata></record> |
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title | Water-mediated and promoted eco-friendly one-pot synthesis of azaarene substituted isoxazolesElectronic supplementary information (ESI) available. See DOI: 10.1039/c7nj01165b |
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