Eco-friendly, Water Mediated, One-Pot Synthesis of 2-(5,6-Dicyano-1H-benzo[d]imidazol-2-yl)-N-arylbenzamides and Their Antifungal Activity Testing
Abstract Ecofriendly, water mediated, one-pot three-component synthesis of novel 2-(5,6-dicyano-1H-benzo[d]imidazol-2-yl)-N-arylbenzamides have been developed by the reactions of phthalic anhydride with substituted anilines and 4,5-diaminophthalonitrile in water for 90–120 min at 100°C without any c...
Ausführliche Beschreibung
Gespeichert in:
| Autor*in: |
Narayana, B. S. [verfasserIn] |
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| Format: |
E-Artikel |
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| Sprache: |
Englisch |
| Erschienen: |
2023 |
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| Anmerkung: |
© Pleiades Publishing, Ltd. 2023 |
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| Übergeordnetes Werk: |
Enthalten in: Russian journal of organic chemistry - Dordrecht : Springer Science + Business Media B.V., 1996, 59(2023), 2 vom: Feb., Seite 305-311 |
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| Übergeordnetes Werk: |
volume:59 ; year:2023 ; number:2 ; month:02 ; pages:305-311 |
| Links: |
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| DOI / URN: |
10.1134/S1070428023020124 |
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| Katalog-ID: |
SPR050180592 |
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| 100 | 1 | |a Narayana, B. S. |e verfasserin |4 aut | |
| 245 | 1 | 0 | |a Eco-friendly, Water Mediated, One-Pot Synthesis of 2-(5,6-Dicyano-1H-benzo[d]imidazol-2-yl)-N-arylbenzamides and Their Antifungal Activity Testing |
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| 520 | |a Abstract Ecofriendly, water mediated, one-pot three-component synthesis of novel 2-(5,6-dicyano-1H-benzo[d]imidazol-2-yl)-N-arylbenzamides have been developed by the reactions of phthalic anhydride with substituted anilines and 4,5-diaminophthalonitrile in water for 90–120 min at 100°C without any catalyst. The reactions involve easy workup, provide excellent yields, and use water as a green solvent. | ||
| 700 | 1 | |a Reddy, Y. D. |4 aut | |
| 700 | 1 | |a Reddy, Ch. V. R. |4 aut | |
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10.1134/S1070428023020124 doi (DE-627)SPR050180592 (SPR)S1070428023020124-e DE-627 ger DE-627 rakwb eng Narayana, B. S. verfasserin aut Eco-friendly, Water Mediated, One-Pot Synthesis of 2-(5,6-Dicyano-1H-benzo[d]imidazol-2-yl)-N-arylbenzamides and Their Antifungal Activity Testing 2023 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Pleiades Publishing, Ltd. 2023 Abstract Ecofriendly, water mediated, one-pot three-component synthesis of novel 2-(5,6-dicyano-1H-benzo[d]imidazol-2-yl)-N-arylbenzamides have been developed by the reactions of phthalic anhydride with substituted anilines and 4,5-diaminophthalonitrile in water for 90–120 min at 100°C without any catalyst. The reactions involve easy workup, provide excellent yields, and use water as a green solvent. Reddy, Y. D. aut Reddy, Ch. V. R. aut Enthalten in Russian journal of organic chemistry Dordrecht : Springer Science + Business Media B.V., 1996 59(2023), 2 vom: Feb., Seite 305-311 (DE-627)340148543 (DE-600)2065669-5 1608-3393 nnns volume:59 year:2023 number:2 month:02 pages:305-311 https://dx.doi.org/10.1134/S1070428023020124 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 AR 59 2023 2 02 305-311 |
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10.1134/S1070428023020124 doi (DE-627)SPR050180592 (SPR)S1070428023020124-e DE-627 ger DE-627 rakwb eng Narayana, B. S. verfasserin aut Eco-friendly, Water Mediated, One-Pot Synthesis of 2-(5,6-Dicyano-1H-benzo[d]imidazol-2-yl)-N-arylbenzamides and Their Antifungal Activity Testing 2023 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Pleiades Publishing, Ltd. 2023 Abstract Ecofriendly, water mediated, one-pot three-component synthesis of novel 2-(5,6-dicyano-1H-benzo[d]imidazol-2-yl)-N-arylbenzamides have been developed by the reactions of phthalic anhydride with substituted anilines and 4,5-diaminophthalonitrile in water for 90–120 min at 100°C without any catalyst. The reactions involve easy workup, provide excellent yields, and use water as a green solvent. Reddy, Y. D. aut Reddy, Ch. V. R. aut Enthalten in Russian journal of organic chemistry Dordrecht : Springer Science + Business Media B.V., 1996 59(2023), 2 vom: Feb., Seite 305-311 (DE-627)340148543 (DE-600)2065669-5 1608-3393 nnns volume:59 year:2023 number:2 month:02 pages:305-311 https://dx.doi.org/10.1134/S1070428023020124 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 AR 59 2023 2 02 305-311 |
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10.1134/S1070428023020124 doi (DE-627)SPR050180592 (SPR)S1070428023020124-e DE-627 ger DE-627 rakwb eng Narayana, B. S. verfasserin aut Eco-friendly, Water Mediated, One-Pot Synthesis of 2-(5,6-Dicyano-1H-benzo[d]imidazol-2-yl)-N-arylbenzamides and Their Antifungal Activity Testing 2023 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Pleiades Publishing, Ltd. 2023 Abstract Ecofriendly, water mediated, one-pot three-component synthesis of novel 2-(5,6-dicyano-1H-benzo[d]imidazol-2-yl)-N-arylbenzamides have been developed by the reactions of phthalic anhydride with substituted anilines and 4,5-diaminophthalonitrile in water for 90–120 min at 100°C without any catalyst. The reactions involve easy workup, provide excellent yields, and use water as a green solvent. Reddy, Y. D. aut Reddy, Ch. V. R. aut Enthalten in Russian journal of organic chemistry Dordrecht : Springer Science + Business Media B.V., 1996 59(2023), 2 vom: Feb., Seite 305-311 (DE-627)340148543 (DE-600)2065669-5 1608-3393 nnns volume:59 year:2023 number:2 month:02 pages:305-311 https://dx.doi.org/10.1134/S1070428023020124 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 AR 59 2023 2 02 305-311 |
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Narayana, B. S. Eco-friendly, Water Mediated, One-Pot Synthesis of 2-(5,6-Dicyano-1H-benzo[d]imidazol-2-yl)-N-arylbenzamides and Their Antifungal Activity Testing |
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eco-friendly, water mediated, one-pot synthesis of 2-(5,6-dicyano-1h-benzo[d]imidazol-2-yl)-n-arylbenzamides and their antifungal activity testing |
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Eco-friendly, Water Mediated, One-Pot Synthesis of 2-(5,6-Dicyano-1H-benzo[d]imidazol-2-yl)-N-arylbenzamides and Their Antifungal Activity Testing |
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Abstract Ecofriendly, water mediated, one-pot three-component synthesis of novel 2-(5,6-dicyano-1H-benzo[d]imidazol-2-yl)-N-arylbenzamides have been developed by the reactions of phthalic anhydride with substituted anilines and 4,5-diaminophthalonitrile in water for 90–120 min at 100°C without any catalyst. The reactions involve easy workup, provide excellent yields, and use water as a green solvent. © Pleiades Publishing, Ltd. 2023 |
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Abstract Ecofriendly, water mediated, one-pot three-component synthesis of novel 2-(5,6-dicyano-1H-benzo[d]imidazol-2-yl)-N-arylbenzamides have been developed by the reactions of phthalic anhydride with substituted anilines and 4,5-diaminophthalonitrile in water for 90–120 min at 100°C without any catalyst. The reactions involve easy workup, provide excellent yields, and use water as a green solvent. © Pleiades Publishing, Ltd. 2023 |
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Abstract Ecofriendly, water mediated, one-pot three-component synthesis of novel 2-(5,6-dicyano-1H-benzo[d]imidazol-2-yl)-N-arylbenzamides have been developed by the reactions of phthalic anhydride with substituted anilines and 4,5-diaminophthalonitrile in water for 90–120 min at 100°C without any catalyst. The reactions involve easy workup, provide excellent yields, and use water as a green solvent. © Pleiades Publishing, Ltd. 2023 |
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Eco-friendly, Water Mediated, One-Pot Synthesis of 2-(5,6-Dicyano-1H-benzo[d]imidazol-2-yl)-N-arylbenzamides and Their Antifungal Activity Testing |
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| score |
7.4006968 |