Saccharin: an efficient organocatalyst for the one-pot synthesis of 4-amidocinnolines under metal and halogen-free conditions
Abstract A mild and efficient protocol for the one-pot synthesis of 4-amidocinnolines was developed using saccharin as a cheap and eco-friendly organocatalyst and t-butyl nitrite as a metal-free diazotization reagent. The current method has advantages such as cost effectiveness, use of the biodegrad...
Ausführliche Beschreibung
Gespeichert in:
| Autor*in: |
Khaligh, Nader Ghaffari [verfasserIn] Mihankhah, Taraneh [verfasserIn] Johan, Mohad Rafie [verfasserIn] Ching, Juan Joon [verfasserIn] |
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| Format: |
E-Artikel |
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| Sprache: |
Englisch |
| Erschienen: |
2018 |
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| Schlagwörter: |
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| Übergeordnetes Werk: |
Enthalten in: Monatshefte für Chemie - Wien [u.a.] : Springer, 1880, 149(2018), 6 vom: 21. Feb., Seite 1083-1087 |
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| Übergeordnetes Werk: |
volume:149 ; year:2018 ; number:6 ; day:21 ; month:02 ; pages:1083-1087 |
| Links: |
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| DOI / URN: |
10.1007/s00706-018-2174-2 |
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| Katalog-ID: |
SPR007480377 |
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| 100 | 1 | |a Khaligh, Nader Ghaffari |e verfasserin |4 aut | |
| 245 | 1 | 0 | |a Saccharin: an efficient organocatalyst for the one-pot synthesis of 4-amidocinnolines under metal and halogen-free conditions |
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| 520 | |a Abstract A mild and efficient protocol for the one-pot synthesis of 4-amidocinnolines was developed using saccharin as a cheap and eco-friendly organocatalyst and t-butyl nitrite as a metal-free diazotization reagent. The current method has advantages such as cost effectiveness, use of the biodegradable reagents, simple experimental procedure; afford the quantitative yield of the desired products, metal- and halogen-free as well as environmentally benign conditions. Graphical abstract | ||
| 650 | 4 | |a Saccharin |7 (dpeaa)DE-He213 | |
| 650 | 4 | |a -Butyl nitrite |7 (dpeaa)DE-He213 | |
| 650 | 4 | |a Cinnoline |7 (dpeaa)DE-He213 | |
| 650 | 4 | |a Metal-free condition |7 (dpeaa)DE-He213 | |
| 650 | 4 | |a One-pot synthesis |7 (dpeaa)DE-He213 | |
| 700 | 1 | |a Mihankhah, Taraneh |e verfasserin |4 aut | |
| 700 | 1 | |a Johan, Mohad Rafie |e verfasserin |4 aut | |
| 700 | 1 | |a Ching, Juan Joon |e verfasserin |4 aut | |
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10.1007/s00706-018-2174-2 doi (DE-627)SPR007480377 (SPR)s00706-018-2174-2-e DE-627 ger DE-627 rakwb eng 540 ASE 35.00 bkl Khaligh, Nader Ghaffari verfasserin aut Saccharin: an efficient organocatalyst for the one-pot synthesis of 4-amidocinnolines under metal and halogen-free conditions 2018 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract A mild and efficient protocol for the one-pot synthesis of 4-amidocinnolines was developed using saccharin as a cheap and eco-friendly organocatalyst and t-butyl nitrite as a metal-free diazotization reagent. The current method has advantages such as cost effectiveness, use of the biodegradable reagents, simple experimental procedure; afford the quantitative yield of the desired products, metal- and halogen-free as well as environmentally benign conditions. Graphical abstract Saccharin (dpeaa)DE-He213 -Butyl nitrite (dpeaa)DE-He213 Cinnoline (dpeaa)DE-He213 Metal-free condition (dpeaa)DE-He213 One-pot synthesis (dpeaa)DE-He213 Mihankhah, Taraneh verfasserin aut Johan, Mohad Rafie verfasserin aut Ching, Juan Joon verfasserin aut Enthalten in Monatshefte für Chemie Wien [u.a.] : Springer, 1880 149(2018), 6 vom: 21. Feb., Seite 1083-1087 (DE-627)25462992X (DE-600)1462037-6 1434-4475 nnns volume:149 year:2018 number:6 day:21 month:02 pages:1083-1087 https://dx.doi.org/10.1007/s00706-018-2174-2 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A 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_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_267 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_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 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_2116 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_4012 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_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 35.00 ASE AR 149 2018 6 21 02 1083-1087 |
| spelling |
10.1007/s00706-018-2174-2 doi (DE-627)SPR007480377 (SPR)s00706-018-2174-2-e DE-627 ger DE-627 rakwb eng 540 ASE 35.00 bkl Khaligh, Nader Ghaffari verfasserin aut Saccharin: an efficient organocatalyst for the one-pot synthesis of 4-amidocinnolines under metal and halogen-free conditions 2018 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract A mild and efficient protocol for the one-pot synthesis of 4-amidocinnolines was developed using saccharin as a cheap and eco-friendly organocatalyst and t-butyl nitrite as a metal-free diazotization reagent. The current method has advantages such as cost effectiveness, use of the biodegradable reagents, simple experimental procedure; afford the quantitative yield of the desired products, metal- and halogen-free as well as environmentally benign conditions. Graphical abstract Saccharin (dpeaa)DE-He213 -Butyl nitrite (dpeaa)DE-He213 Cinnoline (dpeaa)DE-He213 Metal-free condition (dpeaa)DE-He213 One-pot synthesis (dpeaa)DE-He213 Mihankhah, Taraneh verfasserin aut Johan, Mohad Rafie verfasserin aut Ching, Juan Joon verfasserin aut Enthalten in Monatshefte für Chemie Wien [u.a.] : Springer, 1880 149(2018), 6 vom: 21. Feb., Seite 1083-1087 (DE-627)25462992X (DE-600)1462037-6 1434-4475 nnns volume:149 year:2018 number:6 day:21 month:02 pages:1083-1087 https://dx.doi.org/10.1007/s00706-018-2174-2 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A 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_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_267 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_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 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_2116 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_4012 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_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 35.00 ASE AR 149 2018 6 21 02 1083-1087 |
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10.1007/s00706-018-2174-2 doi (DE-627)SPR007480377 (SPR)s00706-018-2174-2-e DE-627 ger DE-627 rakwb eng 540 ASE 35.00 bkl Khaligh, Nader Ghaffari verfasserin aut Saccharin: an efficient organocatalyst for the one-pot synthesis of 4-amidocinnolines under metal and halogen-free conditions 2018 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract A mild and efficient protocol for the one-pot synthesis of 4-amidocinnolines was developed using saccharin as a cheap and eco-friendly organocatalyst and t-butyl nitrite as a metal-free diazotization reagent. The current method has advantages such as cost effectiveness, use of the biodegradable reagents, simple experimental procedure; afford the quantitative yield of the desired products, metal- and halogen-free as well as environmentally benign conditions. Graphical abstract Saccharin (dpeaa)DE-He213 -Butyl nitrite (dpeaa)DE-He213 Cinnoline (dpeaa)DE-He213 Metal-free condition (dpeaa)DE-He213 One-pot synthesis (dpeaa)DE-He213 Mihankhah, Taraneh verfasserin aut Johan, Mohad Rafie verfasserin aut Ching, Juan Joon verfasserin aut Enthalten in Monatshefte für Chemie Wien [u.a.] : Springer, 1880 149(2018), 6 vom: 21. Feb., Seite 1083-1087 (DE-627)25462992X (DE-600)1462037-6 1434-4475 nnns volume:149 year:2018 number:6 day:21 month:02 pages:1083-1087 https://dx.doi.org/10.1007/s00706-018-2174-2 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A 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_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_267 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_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 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_2116 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_4012 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_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 35.00 ASE AR 149 2018 6 21 02 1083-1087 |
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10.1007/s00706-018-2174-2 doi (DE-627)SPR007480377 (SPR)s00706-018-2174-2-e DE-627 ger DE-627 rakwb eng 540 ASE 35.00 bkl Khaligh, Nader Ghaffari verfasserin aut Saccharin: an efficient organocatalyst for the one-pot synthesis of 4-amidocinnolines under metal and halogen-free conditions 2018 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract A mild and efficient protocol for the one-pot synthesis of 4-amidocinnolines was developed using saccharin as a cheap and eco-friendly organocatalyst and t-butyl nitrite as a metal-free diazotization reagent. The current method has advantages such as cost effectiveness, use of the biodegradable reagents, simple experimental procedure; afford the quantitative yield of the desired products, metal- and halogen-free as well as environmentally benign conditions. Graphical abstract Saccharin (dpeaa)DE-He213 -Butyl nitrite (dpeaa)DE-He213 Cinnoline (dpeaa)DE-He213 Metal-free condition (dpeaa)DE-He213 One-pot synthesis (dpeaa)DE-He213 Mihankhah, Taraneh verfasserin aut Johan, Mohad Rafie verfasserin aut Ching, Juan Joon verfasserin aut Enthalten in Monatshefte für Chemie Wien [u.a.] : Springer, 1880 149(2018), 6 vom: 21. Feb., Seite 1083-1087 (DE-627)25462992X (DE-600)1462037-6 1434-4475 nnns volume:149 year:2018 number:6 day:21 month:02 pages:1083-1087 https://dx.doi.org/10.1007/s00706-018-2174-2 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A 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_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_267 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_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 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_2116 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_4012 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_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 35.00 ASE AR 149 2018 6 21 02 1083-1087 |
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10.1007/s00706-018-2174-2 doi (DE-627)SPR007480377 (SPR)s00706-018-2174-2-e DE-627 ger DE-627 rakwb eng 540 ASE 35.00 bkl Khaligh, Nader Ghaffari verfasserin aut Saccharin: an efficient organocatalyst for the one-pot synthesis of 4-amidocinnolines under metal and halogen-free conditions 2018 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract A mild and efficient protocol for the one-pot synthesis of 4-amidocinnolines was developed using saccharin as a cheap and eco-friendly organocatalyst and t-butyl nitrite as a metal-free diazotization reagent. The current method has advantages such as cost effectiveness, use of the biodegradable reagents, simple experimental procedure; afford the quantitative yield of the desired products, metal- and halogen-free as well as environmentally benign conditions. Graphical abstract Saccharin (dpeaa)DE-He213 -Butyl nitrite (dpeaa)DE-He213 Cinnoline (dpeaa)DE-He213 Metal-free condition (dpeaa)DE-He213 One-pot synthesis (dpeaa)DE-He213 Mihankhah, Taraneh verfasserin aut Johan, Mohad Rafie verfasserin aut Ching, Juan Joon verfasserin aut Enthalten in Monatshefte für Chemie Wien [u.a.] : Springer, 1880 149(2018), 6 vom: 21. Feb., Seite 1083-1087 (DE-627)25462992X (DE-600)1462037-6 1434-4475 nnns volume:149 year:2018 number:6 day:21 month:02 pages:1083-1087 https://dx.doi.org/10.1007/s00706-018-2174-2 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A 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_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_267 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_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 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_2116 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_4012 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_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 35.00 ASE AR 149 2018 6 21 02 1083-1087 |
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Enthalten in Monatshefte für Chemie 149(2018), 6 vom: 21. Feb., Seite 1083-1087 volume:149 year:2018 number:6 day:21 month:02 pages:1083-1087 |
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Enthalten in Monatshefte für Chemie 149(2018), 6 vom: 21. Feb., Seite 1083-1087 volume:149 year:2018 number:6 day:21 month:02 pages:1083-1087 |
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findex.gbv.de |
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Saccharin -Butyl nitrite Cinnoline Metal-free condition One-pot synthesis |
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Monatshefte für Chemie |
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Khaligh, Nader Ghaffari @@aut@@ Mihankhah, Taraneh @@aut@@ Johan, Mohad Rafie @@aut@@ Ching, Juan Joon @@aut@@ |
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2018-02-21T00:00:00Z |
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SPR007480377 |
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| author |
Khaligh, Nader Ghaffari |
| spellingShingle |
Khaligh, Nader Ghaffari ddc 540 bkl 35.00 misc Saccharin misc -Butyl nitrite misc Cinnoline misc Metal-free condition misc One-pot synthesis Saccharin: an efficient organocatalyst for the one-pot synthesis of 4-amidocinnolines under metal and halogen-free conditions |
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540 ASE 35.00 bkl Saccharin: an efficient organocatalyst for the one-pot synthesis of 4-amidocinnolines under metal and halogen-free conditions Saccharin (dpeaa)DE-He213 -Butyl nitrite (dpeaa)DE-He213 Cinnoline (dpeaa)DE-He213 Metal-free condition (dpeaa)DE-He213 One-pot synthesis (dpeaa)DE-He213 |
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ddc 540 bkl 35.00 misc Saccharin misc -Butyl nitrite misc Cinnoline misc Metal-free condition misc One-pot synthesis |
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ddc 540 bkl 35.00 misc Saccharin misc -Butyl nitrite misc Cinnoline misc Metal-free condition misc One-pot synthesis |
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ddc 540 bkl 35.00 misc Saccharin misc -Butyl nitrite misc Cinnoline misc Metal-free condition misc One-pot synthesis |
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Elektronische Aufsätze Aufsätze Elektronische Ressource |
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Saccharin: an efficient organocatalyst for the one-pot synthesis of 4-amidocinnolines under metal and halogen-free conditions |
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(DE-627)SPR007480377 (SPR)s00706-018-2174-2-e |
| title_full |
Saccharin: an efficient organocatalyst for the one-pot synthesis of 4-amidocinnolines under metal and halogen-free conditions |
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Khaligh, Nader Ghaffari |
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Monatshefte für Chemie |
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Khaligh, Nader Ghaffari Mihankhah, Taraneh Johan, Mohad Rafie Ching, Juan Joon |
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540 ASE 35.00 bkl |
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Elektronische Aufsätze |
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Khaligh, Nader Ghaffari |
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10.1007/s00706-018-2174-2 |
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verfasserin |
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saccharin: an efficient organocatalyst for the one-pot synthesis of 4-amidocinnolines under metal and halogen-free conditions |
| title_auth |
Saccharin: an efficient organocatalyst for the one-pot synthesis of 4-amidocinnolines under metal and halogen-free conditions |
| abstract |
Abstract A mild and efficient protocol for the one-pot synthesis of 4-amidocinnolines was developed using saccharin as a cheap and eco-friendly organocatalyst and t-butyl nitrite as a metal-free diazotization reagent. The current method has advantages such as cost effectiveness, use of the biodegradable reagents, simple experimental procedure; afford the quantitative yield of the desired products, metal- and halogen-free as well as environmentally benign conditions. Graphical abstract |
| abstractGer |
Abstract A mild and efficient protocol for the one-pot synthesis of 4-amidocinnolines was developed using saccharin as a cheap and eco-friendly organocatalyst and t-butyl nitrite as a metal-free diazotization reagent. The current method has advantages such as cost effectiveness, use of the biodegradable reagents, simple experimental procedure; afford the quantitative yield of the desired products, metal- and halogen-free as well as environmentally benign conditions. Graphical abstract |
| abstract_unstemmed |
Abstract A mild and efficient protocol for the one-pot synthesis of 4-amidocinnolines was developed using saccharin as a cheap and eco-friendly organocatalyst and t-butyl nitrite as a metal-free diazotization reagent. The current method has advantages such as cost effectiveness, use of the biodegradable reagents, simple experimental procedure; afford the quantitative yield of the desired products, metal- and halogen-free as well as environmentally benign conditions. Graphical abstract |
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| title_short |
Saccharin: an efficient organocatalyst for the one-pot synthesis of 4-amidocinnolines under metal and halogen-free conditions |
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https://dx.doi.org/10.1007/s00706-018-2174-2 |
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Mihankhah, Taraneh Johan, Mohad Rafie Ching, Juan Joon |
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Mihankhah, Taraneh Johan, Mohad Rafie Ching, Juan Joon |
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| doi_str |
10.1007/s00706-018-2174-2 |
| up_date |
2024-07-04T03:24:15.993Z |
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|
| score |
7.4012003 |