An efficient ligand- and copper-free Sonogashira reaction catalyzed by palladium nanoparticles supported on pectin
A novel and green procedure for synthesis of Palladium nanoparticles (2–6nm) supported on pectin, as a reductant and ligand is described. The synthesized catalyst was further successfully explored in copper, ligand- and amine-free Sonogashira–Hagihara coupling of various aryl iodides, bromides and c...
Ausführliche Beschreibung
Gespeichert in:
| Autor*in: |
Khazaei, Ardeshir [verfasserIn] |
|---|
| Format: |
E-Artikel |
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| Sprache: |
Englisch |
| Erschienen: |
2013transfer abstract |
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| Umfang: |
5 |
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| Übergeordnetes Werk: |
Enthalten in: Using the Japanese version of the brief assessment of cognition in schizophrenia (BACS-J) to assess cognitive function in patients with REM sleep behavior disorder - Ubara, A. ELSEVIER, 2019, Amsterdam |
|---|---|
| Übergeordnetes Werk: |
volume:37 ; year:2013 ; day:5 ; month:07 ; pages:9-13 ; extent:5 |
| Links: |
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| DOI / URN: |
10.1016/j.catcom.2013.03.013 |
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| 520 | |a A novel and green procedure for synthesis of Palladium nanoparticles (2–6nm) supported on pectin, as a reductant and ligand is described. The synthesized catalyst was further successfully explored in copper, ligand- and amine-free Sonogashira–Hagihara coupling of various aryl iodides, bromides and chlorides as well as heteroaryl halides with phenylacetylene under aerobic conditions. It was found that the catalyst exhibited a high activity and selectivity for the Sonogashira–Hagihara reaction. The catalyst can be recovered and recycled by a simple filtration of the reaction solution with some decrease in catalytic activity. | ||
| 520 | |a A novel and green procedure for synthesis of Palladium nanoparticles (2–6nm) supported on pectin, as a reductant and ligand is described. The synthesized catalyst was further successfully explored in copper, ligand- and amine-free Sonogashira–Hagihara coupling of various aryl iodides, bromides and chlorides as well as heteroaryl halides with phenylacetylene under aerobic conditions. It was found that the catalyst exhibited a high activity and selectivity for the Sonogashira–Hagihara reaction. The catalyst can be recovered and recycled by a simple filtration of the reaction solution with some decrease in catalytic activity. | ||
| 700 | 1 | |a Rahmati, Sadegh |4 oth | |
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10.1016/j.catcom.2013.03.013 doi GBVA2013006000014.pica (DE-627)ELV027112977 (ELSEVIER)S1566-7367(13)00090-3 DE-627 ger DE-627 rakwb eng 660 540 660 DE-600 540 DE-600 610 VZ 44.90 bkl Khazaei, Ardeshir verfasserin aut An efficient ligand- and copper-free Sonogashira reaction catalyzed by palladium nanoparticles supported on pectin 2013transfer abstract 5 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier A novel and green procedure for synthesis of Palladium nanoparticles (2–6nm) supported on pectin, as a reductant and ligand is described. The synthesized catalyst was further successfully explored in copper, ligand- and amine-free Sonogashira–Hagihara coupling of various aryl iodides, bromides and chlorides as well as heteroaryl halides with phenylacetylene under aerobic conditions. It was found that the catalyst exhibited a high activity and selectivity for the Sonogashira–Hagihara reaction. The catalyst can be recovered and recycled by a simple filtration of the reaction solution with some decrease in catalytic activity. A novel and green procedure for synthesis of Palladium nanoparticles (2–6nm) supported on pectin, as a reductant and ligand is described. The synthesized catalyst was further successfully explored in copper, ligand- and amine-free Sonogashira–Hagihara coupling of various aryl iodides, bromides and chlorides as well as heteroaryl halides with phenylacetylene under aerobic conditions. It was found that the catalyst exhibited a high activity and selectivity for the Sonogashira–Hagihara reaction. The catalyst can be recovered and recycled by a simple filtration of the reaction solution with some decrease in catalytic activity. Rahmati, Sadegh oth Saednia, Shahnaz oth Enthalten in Elsevier Ubara, A. ELSEVIER Using the Japanese version of the brief assessment of cognition in schizophrenia (BACS-J) to assess cognitive function in patients with REM sleep behavior disorder 2019 Amsterdam (DE-627)ELV003313131 volume:37 year:2013 day:5 month:07 pages:9-13 extent:5 https://doi.org/10.1016/j.catcom.2013.03.013 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U SSG-OLC-PHA 44.90 Neurologie VZ AR 37 2013 5 0705 9-13 5 045F 660 |
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An efficient ligand- and copper-free Sonogashira reaction catalyzed by palladium nanoparticles supported on pectin |
| abstract |
A novel and green procedure for synthesis of Palladium nanoparticles (2–6nm) supported on pectin, as a reductant and ligand is described. The synthesized catalyst was further successfully explored in copper, ligand- and amine-free Sonogashira–Hagihara coupling of various aryl iodides, bromides and chlorides as well as heteroaryl halides with phenylacetylene under aerobic conditions. It was found that the catalyst exhibited a high activity and selectivity for the Sonogashira–Hagihara reaction. The catalyst can be recovered and recycled by a simple filtration of the reaction solution with some decrease in catalytic activity. |
| abstractGer |
A novel and green procedure for synthesis of Palladium nanoparticles (2–6nm) supported on pectin, as a reductant and ligand is described. The synthesized catalyst was further successfully explored in copper, ligand- and amine-free Sonogashira–Hagihara coupling of various aryl iodides, bromides and chlorides as well as heteroaryl halides with phenylacetylene under aerobic conditions. It was found that the catalyst exhibited a high activity and selectivity for the Sonogashira–Hagihara reaction. The catalyst can be recovered and recycled by a simple filtration of the reaction solution with some decrease in catalytic activity. |
| abstract_unstemmed |
A novel and green procedure for synthesis of Palladium nanoparticles (2–6nm) supported on pectin, as a reductant and ligand is described. The synthesized catalyst was further successfully explored in copper, ligand- and amine-free Sonogashira–Hagihara coupling of various aryl iodides, bromides and chlorides as well as heteroaryl halides with phenylacetylene under aerobic conditions. It was found that the catalyst exhibited a high activity and selectivity for the Sonogashira–Hagihara reaction. The catalyst can be recovered and recycled by a simple filtration of the reaction solution with some decrease in catalytic activity. |
| collection_details |
GBV_USEFLAG_U GBV_ELV SYSFLAG_U SSG-OLC-PHA |
| title_short |
An efficient ligand- and copper-free Sonogashira reaction catalyzed by palladium nanoparticles supported on pectin |
| url |
https://doi.org/10.1016/j.catcom.2013.03.013 |
| remote_bool |
true |
| author2 |
Rahmati, Sadegh Saednia, Shahnaz |
| author2Str |
Rahmati, Sadegh Saednia, Shahnaz |
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ELV003313131 |
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| author2_role |
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| doi_str |
10.1016/j.catcom.2013.03.013 |
| up_date |
2024-07-06T21:05:43.311Z |
| _version_ |
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