9-mesityl-10-methylacridinium perchlorate (Mes-Acr-$ Me^{+} $$ ClO_{4} $−) as a novel metal-free donor–acceptor (D–A) photocatalyst: visible-light-induced access to tetrahydrobenzo[b]pyran scaffolds through a single-electron transfer (SET) pathway
Abstract A green radical synthetic approach for the production of tetrahydrobenzo[b]pyran scaffolds, which utilizes a Knoevenagel–Michael cyclocondensation reaction of aldehydes, malononitrile, and dimedone, has been devised. This innovative technique has been designed to achieve environmental susta...
Ausführliche Beschreibung
Gespeichert in:
| Autor*in: |
Mohamadpour, Farzaneh [verfasserIn] Kamyab, Hesam [verfasserIn] Chelliapan, Shreeshivadasan [verfasserIn] Amani, Ali Mohammad [verfasserIn] |
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| Format: |
E-Artikel |
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| Sprache: |
Englisch |
| Erschienen: |
2024 |
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| Schlagwörter: |
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| Anmerkung: |
© The Author(s), under exclusive licence to Springer Nature B.V. 2024. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. |
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| Übergeordnetes Werk: |
Enthalten in: Research on chemical intermediates - Springer Netherlands, 1989, 50(2024), 7 vom: 20. Mai, Seite 2993-3007 |
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| Übergeordnetes Werk: |
volume:50 ; year:2024 ; number:7 ; day:20 ; month:05 ; pages:2993-3007 |
| Links: |
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| DOI / URN: |
10.1007/s11164-024-05304-7 |
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| Katalog-ID: |
SPR056578024 |
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| 520 | |a Abstract A green radical synthetic approach for the production of tetrahydrobenzo[b]pyran scaffolds, which utilizes a Knoevenagel–Michael cyclocondensation reaction of aldehydes, malononitrile, and dimedone, has been devised. This innovative technique has been designed to achieve environmental sustainability. A novel single-electron transfer photocatalyst was employed for the synthesis in an aqueous ethanol solution under an air atmosphere at room temperature and stimulated with blue LED illumination serving as a renewable energy source. The objective of this undertaking is to cultivate a metal-free donor–acceptor (D–A) photocatalyst that is highly affordable and universally accessible. 9-Mesityl-10-methylacridinium perchlorate (Mes-Acr-$ Me^{+} $$ ClO_{4} $−) is recognized for its expeditious and effortless applicability, high efficiency in yielding products, low energy consumption, and commendable eco-friendliness. This capability facilitates the investigation into the temporal alterations of environmental and chemical constituents. A research inquiry was conducted with the primary objective of determining the turnover number and turnover frequency associated with tetrahydrobenzo[b]pyran scaffolds. Furthermore, the attainment of cyclization at a gram-scale level offers substantiation for its feasibility as a viable solution for industrial implementation. | ||
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10.1007/s11164-024-05304-7 doi (DE-627)SPR056578024 (SPR)s11164-024-05304-7-e DE-627 ger DE-627 rakwb eng 540 VZ 35.13 bkl Mohamadpour, Farzaneh verfasserin aut 9-mesityl-10-methylacridinium perchlorate (Mes-Acr-$ Me^{+} $$ ClO_{4} $−) as a novel metal-free donor–acceptor (D–A) photocatalyst: visible-light-induced access to tetrahydrobenzo[b]pyran scaffolds through a single-electron transfer (SET) pathway 2024 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © The Author(s), under exclusive licence to Springer Nature B.V. 2024. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. Abstract A green radical synthetic approach for the production of tetrahydrobenzo[b]pyran scaffolds, which utilizes a Knoevenagel–Michael cyclocondensation reaction of aldehydes, malononitrile, and dimedone, has been devised. This innovative technique has been designed to achieve environmental sustainability. A novel single-electron transfer photocatalyst was employed for the synthesis in an aqueous ethanol solution under an air atmosphere at room temperature and stimulated with blue LED illumination serving as a renewable energy source. The objective of this undertaking is to cultivate a metal-free donor–acceptor (D–A) photocatalyst that is highly affordable and universally accessible. 9-Mesityl-10-methylacridinium perchlorate (Mes-Acr-$ Me^{+} $$ ClO_{4} $−) is recognized for its expeditious and effortless applicability, high efficiency in yielding products, low energy consumption, and commendable eco-friendliness. This capability facilitates the investigation into the temporal alterations of environmental and chemical constituents. A research inquiry was conducted with the primary objective of determining the turnover number and turnover frequency associated with tetrahydrobenzo[b]pyran scaffolds. Furthermore, the attainment of cyclization at a gram-scale level offers substantiation for its feasibility as a viable solution for industrial implementation. 9-Mesityl-10-methylacridinium perchlorate (Mes-Acr-Me (dpeaa)DE-He213 ClO (dpeaa)DE-He213 ) (dpeaa)DE-He213 Electron-transfer pathway (dpeaa)DE-He213 Tetrahydrobenzo[ (dpeaa)DE-He213 ]pyran scaffolds (dpeaa)DE-He213 Renewable energy source (dpeaa)DE-He213 Gram-scale synthesis (dpeaa)DE-He213 Kamyab, Hesam verfasserin aut Chelliapan, Shreeshivadasan verfasserin aut Amani, Ali Mohammad verfasserin aut Enthalten in Research on chemical intermediates Springer Netherlands, 1989 50(2024), 7 vom: 20. Mai, Seite 2993-3007 (DE-627)328186511 (DE-600)2045085-0 1568-5675 nnns volume:50 year:2024 number:7 day:20 month:05 pages:2993-3007 https://dx.doi.org/10.1007/s11164-024-05304-7 X:SPRINGER Resolving-System lizenzpflichtig Volltext SYSFLAG_0 GBV_SPRINGER SSG-OLC-PHA 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_65 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_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_2119 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_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 35.13 VZ AR 50 2024 7 20 05 2993-3007 |
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10.1007/s11164-024-05304-7 doi (DE-627)SPR056578024 (SPR)s11164-024-05304-7-e DE-627 ger DE-627 rakwb eng 540 VZ 35.13 bkl Mohamadpour, Farzaneh verfasserin aut 9-mesityl-10-methylacridinium perchlorate (Mes-Acr-$ Me^{+} $$ ClO_{4} $−) as a novel metal-free donor–acceptor (D–A) photocatalyst: visible-light-induced access to tetrahydrobenzo[b]pyran scaffolds through a single-electron transfer (SET) pathway 2024 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © The Author(s), under exclusive licence to Springer Nature B.V. 2024. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. Abstract A green radical synthetic approach for the production of tetrahydrobenzo[b]pyran scaffolds, which utilizes a Knoevenagel–Michael cyclocondensation reaction of aldehydes, malononitrile, and dimedone, has been devised. This innovative technique has been designed to achieve environmental sustainability. A novel single-electron transfer photocatalyst was employed for the synthesis in an aqueous ethanol solution under an air atmosphere at room temperature and stimulated with blue LED illumination serving as a renewable energy source. The objective of this undertaking is to cultivate a metal-free donor–acceptor (D–A) photocatalyst that is highly affordable and universally accessible. 9-Mesityl-10-methylacridinium perchlorate (Mes-Acr-$ Me^{+} $$ ClO_{4} $−) is recognized for its expeditious and effortless applicability, high efficiency in yielding products, low energy consumption, and commendable eco-friendliness. This capability facilitates the investigation into the temporal alterations of environmental and chemical constituents. A research inquiry was conducted with the primary objective of determining the turnover number and turnover frequency associated with tetrahydrobenzo[b]pyran scaffolds. Furthermore, the attainment of cyclization at a gram-scale level offers substantiation for its feasibility as a viable solution for industrial implementation. 9-Mesityl-10-methylacridinium perchlorate (Mes-Acr-Me (dpeaa)DE-He213 ClO (dpeaa)DE-He213 ) (dpeaa)DE-He213 Electron-transfer pathway (dpeaa)DE-He213 Tetrahydrobenzo[ (dpeaa)DE-He213 ]pyran scaffolds (dpeaa)DE-He213 Renewable energy source (dpeaa)DE-He213 Gram-scale synthesis (dpeaa)DE-He213 Kamyab, Hesam verfasserin aut Chelliapan, Shreeshivadasan verfasserin aut Amani, Ali Mohammad verfasserin aut Enthalten in Research on chemical intermediates Springer Netherlands, 1989 50(2024), 7 vom: 20. Mai, Seite 2993-3007 (DE-627)328186511 (DE-600)2045085-0 1568-5675 nnns volume:50 year:2024 number:7 day:20 month:05 pages:2993-3007 https://dx.doi.org/10.1007/s11164-024-05304-7 X:SPRINGER Resolving-System lizenzpflichtig Volltext SYSFLAG_0 GBV_SPRINGER SSG-OLC-PHA 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_65 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_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_2119 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_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 35.13 VZ AR 50 2024 7 20 05 2993-3007 |
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10.1007/s11164-024-05304-7 doi (DE-627)SPR056578024 (SPR)s11164-024-05304-7-e DE-627 ger DE-627 rakwb eng 540 VZ 35.13 bkl Mohamadpour, Farzaneh verfasserin aut 9-mesityl-10-methylacridinium perchlorate (Mes-Acr-$ Me^{+} $$ ClO_{4} $−) as a novel metal-free donor–acceptor (D–A) photocatalyst: visible-light-induced access to tetrahydrobenzo[b]pyran scaffolds through a single-electron transfer (SET) pathway 2024 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © The Author(s), under exclusive licence to Springer Nature B.V. 2024. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. Abstract A green radical synthetic approach for the production of tetrahydrobenzo[b]pyran scaffolds, which utilizes a Knoevenagel–Michael cyclocondensation reaction of aldehydes, malononitrile, and dimedone, has been devised. This innovative technique has been designed to achieve environmental sustainability. A novel single-electron transfer photocatalyst was employed for the synthesis in an aqueous ethanol solution under an air atmosphere at room temperature and stimulated with blue LED illumination serving as a renewable energy source. The objective of this undertaking is to cultivate a metal-free donor–acceptor (D–A) photocatalyst that is highly affordable and universally accessible. 9-Mesityl-10-methylacridinium perchlorate (Mes-Acr-$ Me^{+} $$ ClO_{4} $−) is recognized for its expeditious and effortless applicability, high efficiency in yielding products, low energy consumption, and commendable eco-friendliness. This capability facilitates the investigation into the temporal alterations of environmental and chemical constituents. A research inquiry was conducted with the primary objective of determining the turnover number and turnover frequency associated with tetrahydrobenzo[b]pyran scaffolds. Furthermore, the attainment of cyclization at a gram-scale level offers substantiation for its feasibility as a viable solution for industrial implementation. 9-Mesityl-10-methylacridinium perchlorate (Mes-Acr-Me (dpeaa)DE-He213 ClO (dpeaa)DE-He213 ) (dpeaa)DE-He213 Electron-transfer pathway (dpeaa)DE-He213 Tetrahydrobenzo[ (dpeaa)DE-He213 ]pyran scaffolds (dpeaa)DE-He213 Renewable energy source (dpeaa)DE-He213 Gram-scale synthesis (dpeaa)DE-He213 Kamyab, Hesam verfasserin aut Chelliapan, Shreeshivadasan verfasserin aut Amani, Ali Mohammad verfasserin aut Enthalten in Research on chemical intermediates Springer Netherlands, 1989 50(2024), 7 vom: 20. Mai, Seite 2993-3007 (DE-627)328186511 (DE-600)2045085-0 1568-5675 nnns volume:50 year:2024 number:7 day:20 month:05 pages:2993-3007 https://dx.doi.org/10.1007/s11164-024-05304-7 X:SPRINGER Resolving-System lizenzpflichtig Volltext SYSFLAG_0 GBV_SPRINGER SSG-OLC-PHA 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_65 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_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_2119 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_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 35.13 VZ AR 50 2024 7 20 05 2993-3007 |
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10.1007/s11164-024-05304-7 doi (DE-627)SPR056578024 (SPR)s11164-024-05304-7-e DE-627 ger DE-627 rakwb eng 540 VZ 35.13 bkl Mohamadpour, Farzaneh verfasserin aut 9-mesityl-10-methylacridinium perchlorate (Mes-Acr-$ Me^{+} $$ ClO_{4} $−) as a novel metal-free donor–acceptor (D–A) photocatalyst: visible-light-induced access to tetrahydrobenzo[b]pyran scaffolds through a single-electron transfer (SET) pathway 2024 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © The Author(s), under exclusive licence to Springer Nature B.V. 2024. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. Abstract A green radical synthetic approach for the production of tetrahydrobenzo[b]pyran scaffolds, which utilizes a Knoevenagel–Michael cyclocondensation reaction of aldehydes, malononitrile, and dimedone, has been devised. This innovative technique has been designed to achieve environmental sustainability. A novel single-electron transfer photocatalyst was employed for the synthesis in an aqueous ethanol solution under an air atmosphere at room temperature and stimulated with blue LED illumination serving as a renewable energy source. The objective of this undertaking is to cultivate a metal-free donor–acceptor (D–A) photocatalyst that is highly affordable and universally accessible. 9-Mesityl-10-methylacridinium perchlorate (Mes-Acr-$ Me^{+} $$ ClO_{4} $−) is recognized for its expeditious and effortless applicability, high efficiency in yielding products, low energy consumption, and commendable eco-friendliness. This capability facilitates the investigation into the temporal alterations of environmental and chemical constituents. A research inquiry was conducted with the primary objective of determining the turnover number and turnover frequency associated with tetrahydrobenzo[b]pyran scaffolds. Furthermore, the attainment of cyclization at a gram-scale level offers substantiation for its feasibility as a viable solution for industrial implementation. 9-Mesityl-10-methylacridinium perchlorate (Mes-Acr-Me (dpeaa)DE-He213 ClO (dpeaa)DE-He213 ) (dpeaa)DE-He213 Electron-transfer pathway (dpeaa)DE-He213 Tetrahydrobenzo[ (dpeaa)DE-He213 ]pyran scaffolds (dpeaa)DE-He213 Renewable energy source (dpeaa)DE-He213 Gram-scale synthesis (dpeaa)DE-He213 Kamyab, Hesam verfasserin aut Chelliapan, Shreeshivadasan verfasserin aut Amani, Ali Mohammad verfasserin aut Enthalten in Research on chemical intermediates Springer Netherlands, 1989 50(2024), 7 vom: 20. Mai, Seite 2993-3007 (DE-627)328186511 (DE-600)2045085-0 1568-5675 nnns volume:50 year:2024 number:7 day:20 month:05 pages:2993-3007 https://dx.doi.org/10.1007/s11164-024-05304-7 X:SPRINGER Resolving-System lizenzpflichtig Volltext SYSFLAG_0 GBV_SPRINGER SSG-OLC-PHA 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_65 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_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_2119 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_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 35.13 VZ AR 50 2024 7 20 05 2993-3007 |
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10.1007/s11164-024-05304-7 doi (DE-627)SPR056578024 (SPR)s11164-024-05304-7-e DE-627 ger DE-627 rakwb eng 540 VZ 35.13 bkl Mohamadpour, Farzaneh verfasserin aut 9-mesityl-10-methylacridinium perchlorate (Mes-Acr-$ Me^{+} $$ ClO_{4} $−) as a novel metal-free donor–acceptor (D–A) photocatalyst: visible-light-induced access to tetrahydrobenzo[b]pyran scaffolds through a single-electron transfer (SET) pathway 2024 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © The Author(s), under exclusive licence to Springer Nature B.V. 2024. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. Abstract A green radical synthetic approach for the production of tetrahydrobenzo[b]pyran scaffolds, which utilizes a Knoevenagel–Michael cyclocondensation reaction of aldehydes, malononitrile, and dimedone, has been devised. This innovative technique has been designed to achieve environmental sustainability. A novel single-electron transfer photocatalyst was employed for the synthesis in an aqueous ethanol solution under an air atmosphere at room temperature and stimulated with blue LED illumination serving as a renewable energy source. The objective of this undertaking is to cultivate a metal-free donor–acceptor (D–A) photocatalyst that is highly affordable and universally accessible. 9-Mesityl-10-methylacridinium perchlorate (Mes-Acr-$ Me^{+} $$ ClO_{4} $−) is recognized for its expeditious and effortless applicability, high efficiency in yielding products, low energy consumption, and commendable eco-friendliness. This capability facilitates the investigation into the temporal alterations of environmental and chemical constituents. A research inquiry was conducted with the primary objective of determining the turnover number and turnover frequency associated with tetrahydrobenzo[b]pyran scaffolds. Furthermore, the attainment of cyclization at a gram-scale level offers substantiation for its feasibility as a viable solution for industrial implementation. 9-Mesityl-10-methylacridinium perchlorate (Mes-Acr-Me (dpeaa)DE-He213 ClO (dpeaa)DE-He213 ) (dpeaa)DE-He213 Electron-transfer pathway (dpeaa)DE-He213 Tetrahydrobenzo[ (dpeaa)DE-He213 ]pyran scaffolds (dpeaa)DE-He213 Renewable energy source (dpeaa)DE-He213 Gram-scale synthesis (dpeaa)DE-He213 Kamyab, Hesam verfasserin aut Chelliapan, Shreeshivadasan verfasserin aut Amani, Ali Mohammad verfasserin aut Enthalten in Research on chemical intermediates Springer Netherlands, 1989 50(2024), 7 vom: 20. Mai, Seite 2993-3007 (DE-627)328186511 (DE-600)2045085-0 1568-5675 nnns volume:50 year:2024 number:7 day:20 month:05 pages:2993-3007 https://dx.doi.org/10.1007/s11164-024-05304-7 X:SPRINGER Resolving-System lizenzpflichtig Volltext SYSFLAG_0 GBV_SPRINGER SSG-OLC-PHA 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_65 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_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_2119 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_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 35.13 VZ AR 50 2024 7 20 05 2993-3007 |
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9-Mesityl-10-methylacridinium perchlorate (Mes-Acr-Me ClO ) Electron-transfer pathway Tetrahydrobenzo[ ]pyran scaffolds Renewable energy source Gram-scale synthesis |
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Mohamadpour, Farzaneh @@aut@@ Kamyab, Hesam @@aut@@ Chelliapan, Shreeshivadasan @@aut@@ Amani, Ali Mohammad @@aut@@ |
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Mohamadpour, Farzaneh |
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Mohamadpour, Farzaneh ddc 540 bkl 35.13 misc 9-Mesityl-10-methylacridinium perchlorate (Mes-Acr-Me misc ClO misc ) misc Electron-transfer pathway misc Tetrahydrobenzo[ misc ]pyran scaffolds misc Renewable energy source misc Gram-scale synthesis 9-mesityl-10-methylacridinium perchlorate (Mes-Acr-$ Me^{+} $$ ClO_{4} $−) as a novel metal-free donor–acceptor (D–A) photocatalyst: visible-light-induced access to tetrahydrobenzo[b]pyran scaffolds through a single-electron transfer (SET) pathway |
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540 VZ 35.13 bkl 9-mesityl-10-methylacridinium perchlorate (Mes-Acr-$ Me^{+} $$ ClO_{4} $−) as a novel metal-free donor–acceptor (D–A) photocatalyst: visible-light-induced access to tetrahydrobenzo[b]pyran scaffolds through a single-electron transfer (SET) pathway 9-Mesityl-10-methylacridinium perchlorate (Mes-Acr-Me (dpeaa)DE-He213 ClO (dpeaa)DE-He213 ) (dpeaa)DE-He213 Electron-transfer pathway (dpeaa)DE-He213 Tetrahydrobenzo[ (dpeaa)DE-He213 ]pyran scaffolds (dpeaa)DE-He213 Renewable energy source (dpeaa)DE-He213 Gram-scale synthesis (dpeaa)DE-He213 |
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ddc 540 bkl 35.13 misc 9-Mesityl-10-methylacridinium perchlorate (Mes-Acr-Me misc ClO misc ) misc Electron-transfer pathway misc Tetrahydrobenzo[ misc ]pyran scaffolds misc Renewable energy source misc Gram-scale synthesis |
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ddc 540 bkl 35.13 misc 9-Mesityl-10-methylacridinium perchlorate (Mes-Acr-Me misc ClO misc ) misc Electron-transfer pathway misc Tetrahydrobenzo[ misc ]pyran scaffolds misc Renewable energy source misc Gram-scale synthesis |
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ddc 540 bkl 35.13 misc 9-Mesityl-10-methylacridinium perchlorate (Mes-Acr-Me misc ClO misc ) misc Electron-transfer pathway misc Tetrahydrobenzo[ misc ]pyran scaffolds misc Renewable energy source misc Gram-scale synthesis |
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9-mesityl-10-methylacridinium perchlorate (Mes-Acr-$ Me^{+} $$ ClO_{4} $−) as a novel metal-free donor–acceptor (D–A) photocatalyst: visible-light-induced access to tetrahydrobenzo[b]pyran scaffolds through a single-electron transfer (SET) pathway |
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9-mesityl-10-methylacridinium perchlorate (Mes-Acr-$ Me^{+} $$ ClO_{4} $−) as a novel metal-free donor–acceptor (D–A) photocatalyst: visible-light-induced access to tetrahydrobenzo[b]pyran scaffolds through a single-electron transfer (SET) pathway |
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Mohamadpour, Farzaneh Kamyab, Hesam Chelliapan, Shreeshivadasan Amani, Ali Mohammad |
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9-mesityl-10-methylacridinium perchlorate (mes-acr-$ me^{+} $$ clo_{4} $−) as a novel metal-free donor–acceptor (d–a) photocatalyst: visible-light-induced access to tetrahydrobenzo[b]pyran scaffolds through a single-electron transfer (set) pathway |
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9-mesityl-10-methylacridinium perchlorate (Mes-Acr-$ Me^{+} $$ ClO_{4} $−) as a novel metal-free donor–acceptor (D–A) photocatalyst: visible-light-induced access to tetrahydrobenzo[b]pyran scaffolds through a single-electron transfer (SET) pathway |
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Abstract A green radical synthetic approach for the production of tetrahydrobenzo[b]pyran scaffolds, which utilizes a Knoevenagel–Michael cyclocondensation reaction of aldehydes, malononitrile, and dimedone, has been devised. This innovative technique has been designed to achieve environmental sustainability. A novel single-electron transfer photocatalyst was employed for the synthesis in an aqueous ethanol solution under an air atmosphere at room temperature and stimulated with blue LED illumination serving as a renewable energy source. The objective of this undertaking is to cultivate a metal-free donor–acceptor (D–A) photocatalyst that is highly affordable and universally accessible. 9-Mesityl-10-methylacridinium perchlorate (Mes-Acr-$ Me^{+} $$ ClO_{4} $−) is recognized for its expeditious and effortless applicability, high efficiency in yielding products, low energy consumption, and commendable eco-friendliness. This capability facilitates the investigation into the temporal alterations of environmental and chemical constituents. A research inquiry was conducted with the primary objective of determining the turnover number and turnover frequency associated with tetrahydrobenzo[b]pyran scaffolds. Furthermore, the attainment of cyclization at a gram-scale level offers substantiation for its feasibility as a viable solution for industrial implementation. © The Author(s), under exclusive licence to Springer Nature B.V. 2024. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. |
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Abstract A green radical synthetic approach for the production of tetrahydrobenzo[b]pyran scaffolds, which utilizes a Knoevenagel–Michael cyclocondensation reaction of aldehydes, malononitrile, and dimedone, has been devised. This innovative technique has been designed to achieve environmental sustainability. A novel single-electron transfer photocatalyst was employed for the synthesis in an aqueous ethanol solution under an air atmosphere at room temperature and stimulated with blue LED illumination serving as a renewable energy source. The objective of this undertaking is to cultivate a metal-free donor–acceptor (D–A) photocatalyst that is highly affordable and universally accessible. 9-Mesityl-10-methylacridinium perchlorate (Mes-Acr-$ Me^{+} $$ ClO_{4} $−) is recognized for its expeditious and effortless applicability, high efficiency in yielding products, low energy consumption, and commendable eco-friendliness. This capability facilitates the investigation into the temporal alterations of environmental and chemical constituents. A research inquiry was conducted with the primary objective of determining the turnover number and turnover frequency associated with tetrahydrobenzo[b]pyran scaffolds. Furthermore, the attainment of cyclization at a gram-scale level offers substantiation for its feasibility as a viable solution for industrial implementation. © The Author(s), under exclusive licence to Springer Nature B.V. 2024. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. |
| abstract_unstemmed |
Abstract A green radical synthetic approach for the production of tetrahydrobenzo[b]pyran scaffolds, which utilizes a Knoevenagel–Michael cyclocondensation reaction of aldehydes, malononitrile, and dimedone, has been devised. This innovative technique has been designed to achieve environmental sustainability. A novel single-electron transfer photocatalyst was employed for the synthesis in an aqueous ethanol solution under an air atmosphere at room temperature and stimulated with blue LED illumination serving as a renewable energy source. The objective of this undertaking is to cultivate a metal-free donor–acceptor (D–A) photocatalyst that is highly affordable and universally accessible. 9-Mesityl-10-methylacridinium perchlorate (Mes-Acr-$ Me^{+} $$ ClO_{4} $−) is recognized for its expeditious and effortless applicability, high efficiency in yielding products, low energy consumption, and commendable eco-friendliness. This capability facilitates the investigation into the temporal alterations of environmental and chemical constituents. A research inquiry was conducted with the primary objective of determining the turnover number and turnover frequency associated with tetrahydrobenzo[b]pyran scaffolds. Furthermore, the attainment of cyclization at a gram-scale level offers substantiation for its feasibility as a viable solution for industrial implementation. © The Author(s), under exclusive licence to Springer Nature B.V. 2024. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. |
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9-mesityl-10-methylacridinium perchlorate (Mes-Acr-$ Me^{+} $$ ClO_{4} $−) as a novel metal-free donor–acceptor (D–A) photocatalyst: visible-light-induced access to tetrahydrobenzo[b]pyran scaffolds through a single-electron transfer (SET) pathway |
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