Synthesis of Pterostilbene through supported-catalyst promoted Mizoroki-Heck reaction, and its transposition in continuous flow reactor
Autor: | Gianluca Casotti, Gabriele Laudadio, Gaetano Angelici, Adriano Carpita, Graziano Fusini, Claudio Evangelisti |
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Přispěvatelé: | Micro Flow Chemistry and Synthetic Meth. |
Jazyk: | angličtina |
Rok vydání: | 2019 |
Předmět: |
Fluid Flow and Transfer Processes
Green chemistry Flow chemistry Mizoroki-heck reaction Pterostilbene Cross-coupling C-C Pterostilbene 010405 organic chemistry Chemistry Continuous flow Mizoroki-heck reaction Organic Chemistry Transposition (telecommunications) Nanochemistry Flow chemistry 010402 general chemistry 01 natural sciences Cross-coupling C-C 0104 chemical sciences Catalysis chemistry.chemical_compound Chemistry (miscellaneous) Heck reaction Organic chemistry |
Zdroj: | Journal of Flow Chemistry, 9(2), 133-143. Akademiai Kiadó |
ISSN: | 2062-249X |
DOI: | 10.1007/s41981-019-00033-0 |
Popis: | 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. [Figure not available: see fulltext.]. |
Databáze: | OpenAIRE |
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