Synthesis of Pterostilbene through supported-catalyst promoted Mizoroki-Heck reaction, and its transposition in continuous flow reactor
Abstract Pterostilbene, an important polyphenolic compound with interesting biological activities, has been efficiently synthesized through a Mizoroki-Heck reaction catalyzed by commercially available Pd catalysts immobilized onto heterogeneous supports. The synthesis has been transposed in a contin...
Ausführliche Beschreibung
Gespeichert in:
| Autor*in: |
Laudadio, Gabriele [verfasserIn] |
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| Format: |
E-Artikel |
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| Sprache: |
Englisch |
| Erschienen: |
2019 |
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| Schlagwörter: |
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| Anmerkung: |
© Akadémiai Kiadó 2019 |
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| Übergeordnetes Werk: |
Enthalten in: Journal of flow chemistry - [Cham] : Springer International Publishing, 2011, 9(2019), 2 vom: 18. Feb., Seite 133-143 |
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| Übergeordnetes Werk: |
volume:9 ; year:2019 ; number:2 ; day:18 ; month:02 ; pages:133-143 |
| Links: |
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| DOI / URN: |
10.1007/s41981-019-00033-0 |
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| Katalog-ID: |
SPR038366266 |
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| 245 | 1 | 0 | |a Synthesis of Pterostilbene through supported-catalyst promoted Mizoroki-Heck reaction, and its transposition in continuous flow reactor |
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| 520 | |a Abstract Pterostilbene, an important polyphenolic compound with interesting biological activities, has been efficiently synthesized through a Mizoroki-Heck reaction catalyzed by commercially available Pd catalysts immobilized onto heterogeneous supports. The synthesis has been transposed in a continuous flow reactor, following two different retrosynthetic approaches. Graphical abstractFlow synthesis of Pterostilbene | ||
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| 650 | 4 | |a Cross-coupling C-C |7 (dpeaa)DE-He213 | |
| 700 | 1 | |a Fusini, Graziano |4 aut | |
| 700 | 1 | |a Casotti, Gianluca |4 aut | |
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| 700 | 1 | |a Angelici, Gaetano |0 (orcid)0000-0002-4397-3449 |4 aut | |
| 700 | 1 | |a Carpita, Adriano |4 aut | |
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10.1007/s41981-019-00033-0 doi (DE-627)SPR038366266 (SPR)s41981-019-00033-0-e DE-627 ger DE-627 rakwb eng Laudadio, Gabriele verfasserin aut Synthesis of Pterostilbene through supported-catalyst promoted Mizoroki-Heck reaction, and its transposition in continuous flow reactor 2019 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Akadémiai Kiadó 2019 Abstract Pterostilbene, an important polyphenolic compound with interesting biological activities, has been efficiently synthesized through a Mizoroki-Heck reaction catalyzed by commercially available Pd catalysts immobilized onto heterogeneous supports. The synthesis has been transposed in a continuous flow reactor, following two different retrosynthetic approaches. Graphical abstractFlow synthesis of Pterostilbene Flow chemistry (dpeaa)DE-He213 Mizoroki-heck reaction (dpeaa)DE-He213 Pterostilbene (dpeaa)DE-He213 Cross-coupling C-C (dpeaa)DE-He213 Fusini, Graziano aut Casotti, Gianluca aut Evangelisti, Claudio aut Angelici, Gaetano (orcid)0000-0002-4397-3449 aut Carpita, Adriano aut Enthalten in Journal of flow chemistry [Cham] : Springer International Publishing, 2011 9(2019), 2 vom: 18. Feb., Seite 133-143 (DE-627)77992262X (DE-600)2759672-2 2063-0212 nnns volume:9 year:2019 number:2 day:18 month:02 pages:133-143 https://dx.doi.org/10.1007/s41981-019-00033-0 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_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_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_266 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_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_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_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 AR 9 2019 2 18 02 133-143 |
| spelling |
10.1007/s41981-019-00033-0 doi (DE-627)SPR038366266 (SPR)s41981-019-00033-0-e DE-627 ger DE-627 rakwb eng Laudadio, Gabriele verfasserin aut Synthesis of Pterostilbene through supported-catalyst promoted Mizoroki-Heck reaction, and its transposition in continuous flow reactor 2019 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Akadémiai Kiadó 2019 Abstract Pterostilbene, an important polyphenolic compound with interesting biological activities, has been efficiently synthesized through a Mizoroki-Heck reaction catalyzed by commercially available Pd catalysts immobilized onto heterogeneous supports. The synthesis has been transposed in a continuous flow reactor, following two different retrosynthetic approaches. Graphical abstractFlow synthesis of Pterostilbene Flow chemistry (dpeaa)DE-He213 Mizoroki-heck reaction (dpeaa)DE-He213 Pterostilbene (dpeaa)DE-He213 Cross-coupling C-C (dpeaa)DE-He213 Fusini, Graziano aut Casotti, Gianluca aut Evangelisti, Claudio aut Angelici, Gaetano (orcid)0000-0002-4397-3449 aut Carpita, Adriano aut Enthalten in Journal of flow chemistry [Cham] : Springer International Publishing, 2011 9(2019), 2 vom: 18. Feb., Seite 133-143 (DE-627)77992262X (DE-600)2759672-2 2063-0212 nnns volume:9 year:2019 number:2 day:18 month:02 pages:133-143 https://dx.doi.org/10.1007/s41981-019-00033-0 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_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_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_266 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_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_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_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 AR 9 2019 2 18 02 133-143 |
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10.1007/s41981-019-00033-0 doi (DE-627)SPR038366266 (SPR)s41981-019-00033-0-e DE-627 ger DE-627 rakwb eng Laudadio, Gabriele verfasserin aut Synthesis of Pterostilbene through supported-catalyst promoted Mizoroki-Heck reaction, and its transposition in continuous flow reactor 2019 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Akadémiai Kiadó 2019 Abstract Pterostilbene, an important polyphenolic compound with interesting biological activities, has been efficiently synthesized through a Mizoroki-Heck reaction catalyzed by commercially available Pd catalysts immobilized onto heterogeneous supports. The synthesis has been transposed in a continuous flow reactor, following two different retrosynthetic approaches. Graphical abstractFlow synthesis of Pterostilbene Flow chemistry (dpeaa)DE-He213 Mizoroki-heck reaction (dpeaa)DE-He213 Pterostilbene (dpeaa)DE-He213 Cross-coupling C-C (dpeaa)DE-He213 Fusini, Graziano aut Casotti, Gianluca aut Evangelisti, Claudio aut Angelici, Gaetano (orcid)0000-0002-4397-3449 aut Carpita, Adriano aut Enthalten in Journal of flow chemistry [Cham] : Springer International Publishing, 2011 9(2019), 2 vom: 18. Feb., Seite 133-143 (DE-627)77992262X (DE-600)2759672-2 2063-0212 nnns volume:9 year:2019 number:2 day:18 month:02 pages:133-143 https://dx.doi.org/10.1007/s41981-019-00033-0 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_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_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_266 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_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_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_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 AR 9 2019 2 18 02 133-143 |
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10.1007/s41981-019-00033-0 doi (DE-627)SPR038366266 (SPR)s41981-019-00033-0-e DE-627 ger DE-627 rakwb eng Laudadio, Gabriele verfasserin aut Synthesis of Pterostilbene through supported-catalyst promoted Mizoroki-Heck reaction, and its transposition in continuous flow reactor 2019 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Akadémiai Kiadó 2019 Abstract Pterostilbene, an important polyphenolic compound with interesting biological activities, has been efficiently synthesized through a Mizoroki-Heck reaction catalyzed by commercially available Pd catalysts immobilized onto heterogeneous supports. The synthesis has been transposed in a continuous flow reactor, following two different retrosynthetic approaches. Graphical abstractFlow synthesis of Pterostilbene Flow chemistry (dpeaa)DE-He213 Mizoroki-heck reaction (dpeaa)DE-He213 Pterostilbene (dpeaa)DE-He213 Cross-coupling C-C (dpeaa)DE-He213 Fusini, Graziano aut Casotti, Gianluca aut Evangelisti, Claudio aut Angelici, Gaetano (orcid)0000-0002-4397-3449 aut Carpita, Adriano aut Enthalten in Journal of flow chemistry [Cham] : Springer International Publishing, 2011 9(2019), 2 vom: 18. Feb., Seite 133-143 (DE-627)77992262X (DE-600)2759672-2 2063-0212 nnns volume:9 year:2019 number:2 day:18 month:02 pages:133-143 https://dx.doi.org/10.1007/s41981-019-00033-0 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_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_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_266 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_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_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_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 AR 9 2019 2 18 02 133-143 |
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10.1007/s41981-019-00033-0 doi (DE-627)SPR038366266 (SPR)s41981-019-00033-0-e DE-627 ger DE-627 rakwb eng Laudadio, Gabriele verfasserin aut Synthesis of Pterostilbene through supported-catalyst promoted Mizoroki-Heck reaction, and its transposition in continuous flow reactor 2019 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Akadémiai Kiadó 2019 Abstract Pterostilbene, an important polyphenolic compound with interesting biological activities, has been efficiently synthesized through a Mizoroki-Heck reaction catalyzed by commercially available Pd catalysts immobilized onto heterogeneous supports. The synthesis has been transposed in a continuous flow reactor, following two different retrosynthetic approaches. Graphical abstractFlow synthesis of Pterostilbene Flow chemistry (dpeaa)DE-He213 Mizoroki-heck reaction (dpeaa)DE-He213 Pterostilbene (dpeaa)DE-He213 Cross-coupling C-C (dpeaa)DE-He213 Fusini, Graziano aut Casotti, Gianluca aut Evangelisti, Claudio aut Angelici, Gaetano (orcid)0000-0002-4397-3449 aut Carpita, Adriano aut Enthalten in Journal of flow chemistry [Cham] : Springer International Publishing, 2011 9(2019), 2 vom: 18. Feb., Seite 133-143 (DE-627)77992262X (DE-600)2759672-2 2063-0212 nnns volume:9 year:2019 number:2 day:18 month:02 pages:133-143 https://dx.doi.org/10.1007/s41981-019-00033-0 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_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_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_266 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_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_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_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 AR 9 2019 2 18 02 133-143 |
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Enthalten in Journal of flow chemistry 9(2019), 2 vom: 18. Feb., Seite 133-143 volume:9 year:2019 number:2 day:18 month:02 pages:133-143 |
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Enthalten in Journal of flow chemistry 9(2019), 2 vom: 18. Feb., Seite 133-143 volume:9 year:2019 number:2 day:18 month:02 pages:133-143 |
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Flow chemistry Mizoroki-heck reaction Pterostilbene Cross-coupling C-C |
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Laudadio, Gabriele @@aut@@ Fusini, Graziano @@aut@@ Casotti, Gianluca @@aut@@ Evangelisti, Claudio @@aut@@ Angelici, Gaetano @@aut@@ Carpita, Adriano @@aut@@ |
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Laudadio, Gabriele |
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Laudadio, Gabriele misc Flow chemistry misc Mizoroki-heck reaction misc Pterostilbene misc Cross-coupling C-C Synthesis of Pterostilbene through supported-catalyst promoted Mizoroki-Heck reaction, and its transposition in continuous flow reactor |
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Synthesis of Pterostilbene through supported-catalyst promoted Mizoroki-Heck reaction, and its transposition in continuous flow reactor Flow chemistry (dpeaa)DE-He213 Mizoroki-heck reaction (dpeaa)DE-He213 Pterostilbene (dpeaa)DE-He213 Cross-coupling C-C (dpeaa)DE-He213 |
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synthesis of pterostilbene through supported-catalyst promoted mizoroki-heck reaction, and its transposition in continuous flow reactor |
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Synthesis of Pterostilbene through supported-catalyst promoted Mizoroki-Heck reaction, and its transposition in continuous flow reactor |
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Abstract Pterostilbene, an important polyphenolic compound with interesting biological activities, has been efficiently synthesized through a Mizoroki-Heck reaction catalyzed by commercially available Pd catalysts immobilized onto heterogeneous supports. The synthesis has been transposed in a continuous flow reactor, following two different retrosynthetic approaches. Graphical abstractFlow synthesis of Pterostilbene © Akadémiai Kiadó 2019 |
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Abstract Pterostilbene, an important polyphenolic compound with interesting biological activities, has been efficiently synthesized through a Mizoroki-Heck reaction catalyzed by commercially available Pd catalysts immobilized onto heterogeneous supports. The synthesis has been transposed in a continuous flow reactor, following two different retrosynthetic approaches. Graphical abstractFlow synthesis of Pterostilbene © Akadémiai Kiadó 2019 |
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Abstract Pterostilbene, an important polyphenolic compound with interesting biological activities, has been efficiently synthesized through a Mizoroki-Heck reaction catalyzed by commercially available Pd catalysts immobilized onto heterogeneous supports. The synthesis has been transposed in a continuous flow reactor, following two different retrosynthetic approaches. Graphical abstractFlow synthesis of Pterostilbene © Akadémiai Kiadó 2019 |
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Synthesis of Pterostilbene through supported-catalyst promoted Mizoroki-Heck reaction, and its transposition in continuous flow reactor |
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The synthesis has been transposed in a continuous flow reactor, following two different retrosynthetic approaches. 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