Alkoxycarbonylation and phenoxycarbonylation reactions catalyzed by a palladium(II) organometallic complex encaged in Y zeolite
Abstract Catalytic routes for synthesis of alkyl benzoates by alkoxycarbonylation reactions and aryl benzoates by phenoxycarbonylation reactions of aryl iodides are described using a palladium–1,10-phenanthroline complex encaged in Y zeolite. Moderate to excellent yields (40–99 %) of various benzoat...
Ausführliche Beschreibung
Gespeichert in:
| Autor*in: |
Mei, Hui [verfasserIn] |
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| Format: |
Artikel |
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| Sprache: |
Englisch |
| Erschienen: |
2014 |
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| Schlagwörter: |
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| Anmerkung: |
© Springer International Publishing Switzerland 2014 |
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| Übergeordnetes Werk: |
Enthalten in: Transition metal chemistry - Springer International Publishing, 1975, 39(2014), 4 vom: 25. März, Seite 443-450 |
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| Übergeordnetes Werk: |
volume:39 ; year:2014 ; number:4 ; day:25 ; month:03 ; pages:443-450 |
| Links: |
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| DOI / URN: |
10.1007/s11243-014-9818-9 |
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OLC2084050391 |
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| 520 | |a Abstract Catalytic routes for synthesis of alkyl benzoates by alkoxycarbonylation reactions and aryl benzoates by phenoxycarbonylation reactions of aryl iodides are described using a palladium–1,10-phenanthroline complex encaged in Y zeolite. Moderate to excellent yields (40–99 %) of various benzoates were obtained at low Pd loadings of 0.6 mol%. The catalyst could be effectively removed from the reaction mixture by a simple filtration process and was reused four times with only minor loss of activity. Furthermore, its catalytic activity was further highlighted by a comparison with another two supported Pd catalysts. The protocol has the advantages of easy handing, moderate to excellent yield, and catalyst recyclability. Graphical Abstract | ||
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| 650 | 4 | |a Phen | |
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| 700 | 1 | |a Li, Guangxing |4 aut | |
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10.1007/s11243-014-9818-9 doi (DE-627)OLC2084050391 (DE-He213)s11243-014-9818-9-p DE-627 ger DE-627 rakwb eng 660 VZ Mei, Hui verfasserin aut Alkoxycarbonylation and phenoxycarbonylation reactions catalyzed by a palladium(II) organometallic complex encaged in Y zeolite 2014 Text txt rdacontent ohne Hilfsmittel zu benutzen n rdamedia Band nc rdacarrier © Springer International Publishing Switzerland 2014 Abstract Catalytic routes for synthesis of alkyl benzoates by alkoxycarbonylation reactions and aryl benzoates by phenoxycarbonylation reactions of aryl iodides are described using a palladium–1,10-phenanthroline complex encaged in Y zeolite. Moderate to excellent yields (40–99 %) of various benzoates were obtained at low Pd loadings of 0.6 mol%. The catalyst could be effectively removed from the reaction mixture by a simple filtration process and was reused four times with only minor loss of activity. Furthermore, its catalytic activity was further highlighted by a comparison with another two supported Pd catalysts. The protocol has the advantages of easy handing, moderate to excellent yield, and catalyst recyclability. Graphical Abstract CDCl3 Phen PdCl2 Aryl Halide Iodobenzene Xiao, Se aut Zhu, Tianwu aut Lei, Yizhu aut Li, Guangxing aut Enthalten in Transition metal chemistry Springer International Publishing, 1975 39(2014), 4 vom: 25. März, Seite 443-450 (DE-627)129605417 (DE-600)242084-3 (DE-576)015099652 0340-4285 nnns volume:39 year:2014 number:4 day:25 month:03 pages:443-450 https://doi.org/10.1007/s11243-014-9818-9 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_OLC SSG-OLC-TEC SSG-OLC-CHE GBV_ILN_70 GBV_ILN_4012 GBV_ILN_4125 AR 39 2014 4 25 03 443-450 |
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10.1007/s11243-014-9818-9 doi (DE-627)OLC2084050391 (DE-He213)s11243-014-9818-9-p DE-627 ger DE-627 rakwb eng 660 VZ Mei, Hui verfasserin aut Alkoxycarbonylation and phenoxycarbonylation reactions catalyzed by a palladium(II) organometallic complex encaged in Y zeolite 2014 Text txt rdacontent ohne Hilfsmittel zu benutzen n rdamedia Band nc rdacarrier © Springer International Publishing Switzerland 2014 Abstract Catalytic routes for synthesis of alkyl benzoates by alkoxycarbonylation reactions and aryl benzoates by phenoxycarbonylation reactions of aryl iodides are described using a palladium–1,10-phenanthroline complex encaged in Y zeolite. Moderate to excellent yields (40–99 %) of various benzoates were obtained at low Pd loadings of 0.6 mol%. The catalyst could be effectively removed from the reaction mixture by a simple filtration process and was reused four times with only minor loss of activity. Furthermore, its catalytic activity was further highlighted by a comparison with another two supported Pd catalysts. The protocol has the advantages of easy handing, moderate to excellent yield, and catalyst recyclability. Graphical Abstract CDCl3 Phen PdCl2 Aryl Halide Iodobenzene Xiao, Se aut Zhu, Tianwu aut Lei, Yizhu aut Li, Guangxing aut Enthalten in Transition metal chemistry Springer International Publishing, 1975 39(2014), 4 vom: 25. März, Seite 443-450 (DE-627)129605417 (DE-600)242084-3 (DE-576)015099652 0340-4285 nnns volume:39 year:2014 number:4 day:25 month:03 pages:443-450 https://doi.org/10.1007/s11243-014-9818-9 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_OLC SSG-OLC-TEC SSG-OLC-CHE GBV_ILN_70 GBV_ILN_4012 GBV_ILN_4125 AR 39 2014 4 25 03 443-450 |
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10.1007/s11243-014-9818-9 doi (DE-627)OLC2084050391 (DE-He213)s11243-014-9818-9-p DE-627 ger DE-627 rakwb eng 660 VZ Mei, Hui verfasserin aut Alkoxycarbonylation and phenoxycarbonylation reactions catalyzed by a palladium(II) organometallic complex encaged in Y zeolite 2014 Text txt rdacontent ohne Hilfsmittel zu benutzen n rdamedia Band nc rdacarrier © Springer International Publishing Switzerland 2014 Abstract Catalytic routes for synthesis of alkyl benzoates by alkoxycarbonylation reactions and aryl benzoates by phenoxycarbonylation reactions of aryl iodides are described using a palladium–1,10-phenanthroline complex encaged in Y zeolite. Moderate to excellent yields (40–99 %) of various benzoates were obtained at low Pd loadings of 0.6 mol%. The catalyst could be effectively removed from the reaction mixture by a simple filtration process and was reused four times with only minor loss of activity. Furthermore, its catalytic activity was further highlighted by a comparison with another two supported Pd catalysts. The protocol has the advantages of easy handing, moderate to excellent yield, and catalyst recyclability. Graphical Abstract CDCl3 Phen PdCl2 Aryl Halide Iodobenzene Xiao, Se aut Zhu, Tianwu aut Lei, Yizhu aut Li, Guangxing aut Enthalten in Transition metal chemistry Springer International Publishing, 1975 39(2014), 4 vom: 25. März, Seite 443-450 (DE-627)129605417 (DE-600)242084-3 (DE-576)015099652 0340-4285 nnns volume:39 year:2014 number:4 day:25 month:03 pages:443-450 https://doi.org/10.1007/s11243-014-9818-9 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_OLC SSG-OLC-TEC SSG-OLC-CHE GBV_ILN_70 GBV_ILN_4012 GBV_ILN_4125 AR 39 2014 4 25 03 443-450 |
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10.1007/s11243-014-9818-9 doi (DE-627)OLC2084050391 (DE-He213)s11243-014-9818-9-p DE-627 ger DE-627 rakwb eng 660 VZ Mei, Hui verfasserin aut Alkoxycarbonylation and phenoxycarbonylation reactions catalyzed by a palladium(II) organometallic complex encaged in Y zeolite 2014 Text txt rdacontent ohne Hilfsmittel zu benutzen n rdamedia Band nc rdacarrier © Springer International Publishing Switzerland 2014 Abstract Catalytic routes for synthesis of alkyl benzoates by alkoxycarbonylation reactions and aryl benzoates by phenoxycarbonylation reactions of aryl iodides are described using a palladium–1,10-phenanthroline complex encaged in Y zeolite. Moderate to excellent yields (40–99 %) of various benzoates were obtained at low Pd loadings of 0.6 mol%. The catalyst could be effectively removed from the reaction mixture by a simple filtration process and was reused four times with only minor loss of activity. Furthermore, its catalytic activity was further highlighted by a comparison with another two supported Pd catalysts. The protocol has the advantages of easy handing, moderate to excellent yield, and catalyst recyclability. Graphical Abstract CDCl3 Phen PdCl2 Aryl Halide Iodobenzene Xiao, Se aut Zhu, Tianwu aut Lei, Yizhu aut Li, Guangxing aut Enthalten in Transition metal chemistry Springer International Publishing, 1975 39(2014), 4 vom: 25. März, Seite 443-450 (DE-627)129605417 (DE-600)242084-3 (DE-576)015099652 0340-4285 nnns volume:39 year:2014 number:4 day:25 month:03 pages:443-450 https://doi.org/10.1007/s11243-014-9818-9 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_OLC SSG-OLC-TEC SSG-OLC-CHE GBV_ILN_70 GBV_ILN_4012 GBV_ILN_4125 AR 39 2014 4 25 03 443-450 |
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10.1007/s11243-014-9818-9 doi (DE-627)OLC2084050391 (DE-He213)s11243-014-9818-9-p DE-627 ger DE-627 rakwb eng 660 VZ Mei, Hui verfasserin aut Alkoxycarbonylation and phenoxycarbonylation reactions catalyzed by a palladium(II) organometallic complex encaged in Y zeolite 2014 Text txt rdacontent ohne Hilfsmittel zu benutzen n rdamedia Band nc rdacarrier © Springer International Publishing Switzerland 2014 Abstract Catalytic routes for synthesis of alkyl benzoates by alkoxycarbonylation reactions and aryl benzoates by phenoxycarbonylation reactions of aryl iodides are described using a palladium–1,10-phenanthroline complex encaged in Y zeolite. Moderate to excellent yields (40–99 %) of various benzoates were obtained at low Pd loadings of 0.6 mol%. The catalyst could be effectively removed from the reaction mixture by a simple filtration process and was reused four times with only minor loss of activity. Furthermore, its catalytic activity was further highlighted by a comparison with another two supported Pd catalysts. The protocol has the advantages of easy handing, moderate to excellent yield, and catalyst recyclability. Graphical Abstract CDCl3 Phen PdCl2 Aryl Halide Iodobenzene Xiao, Se aut Zhu, Tianwu aut Lei, Yizhu aut Li, Guangxing aut Enthalten in Transition metal chemistry Springer International Publishing, 1975 39(2014), 4 vom: 25. März, Seite 443-450 (DE-627)129605417 (DE-600)242084-3 (DE-576)015099652 0340-4285 nnns volume:39 year:2014 number:4 day:25 month:03 pages:443-450 https://doi.org/10.1007/s11243-014-9818-9 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_OLC SSG-OLC-TEC SSG-OLC-CHE GBV_ILN_70 GBV_ILN_4012 GBV_ILN_4125 AR 39 2014 4 25 03 443-450 |
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660 VZ Alkoxycarbonylation and phenoxycarbonylation reactions catalyzed by a palladium(II) organometallic complex encaged in Y zeolite CDCl3 Phen PdCl2 Aryl Halide Iodobenzene |
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alkoxycarbonylation and phenoxycarbonylation reactions catalyzed by a palladium(ii) organometallic complex encaged in y zeolite |
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Alkoxycarbonylation and phenoxycarbonylation reactions catalyzed by a palladium(II) organometallic complex encaged in Y zeolite |
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Abstract Catalytic routes for synthesis of alkyl benzoates by alkoxycarbonylation reactions and aryl benzoates by phenoxycarbonylation reactions of aryl iodides are described using a palladium–1,10-phenanthroline complex encaged in Y zeolite. Moderate to excellent yields (40–99 %) of various benzoates were obtained at low Pd loadings of 0.6 mol%. The catalyst could be effectively removed from the reaction mixture by a simple filtration process and was reused four times with only minor loss of activity. Furthermore, its catalytic activity was further highlighted by a comparison with another two supported Pd catalysts. The protocol has the advantages of easy handing, moderate to excellent yield, and catalyst recyclability. Graphical Abstract © Springer International Publishing Switzerland 2014 |
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Abstract Catalytic routes for synthesis of alkyl benzoates by alkoxycarbonylation reactions and aryl benzoates by phenoxycarbonylation reactions of aryl iodides are described using a palladium–1,10-phenanthroline complex encaged in Y zeolite. Moderate to excellent yields (40–99 %) of various benzoates were obtained at low Pd loadings of 0.6 mol%. The catalyst could be effectively removed from the reaction mixture by a simple filtration process and was reused four times with only minor loss of activity. Furthermore, its catalytic activity was further highlighted by a comparison with another two supported Pd catalysts. The protocol has the advantages of easy handing, moderate to excellent yield, and catalyst recyclability. Graphical Abstract © Springer International Publishing Switzerland 2014 |
| abstract_unstemmed |
Abstract Catalytic routes for synthesis of alkyl benzoates by alkoxycarbonylation reactions and aryl benzoates by phenoxycarbonylation reactions of aryl iodides are described using a palladium–1,10-phenanthroline complex encaged in Y zeolite. Moderate to excellent yields (40–99 %) of various benzoates were obtained at low Pd loadings of 0.6 mol%. The catalyst could be effectively removed from the reaction mixture by a simple filtration process and was reused four times with only minor loss of activity. Furthermore, its catalytic activity was further highlighted by a comparison with another two supported Pd catalysts. The protocol has the advantages of easy handing, moderate to excellent yield, and catalyst recyclability. Graphical Abstract © Springer International Publishing Switzerland 2014 |
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Alkoxycarbonylation and phenoxycarbonylation reactions catalyzed by a palladium(II) organometallic complex encaged in Y zeolite |
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Xiao, Se Zhu, Tianwu Lei, Yizhu Li, Guangxing |
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Xiao, Se Zhu, Tianwu Lei, Yizhu Li, Guangxing |
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129605417 |
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| doi_str |
10.1007/s11243-014-9818-9 |
| up_date |
2024-07-04T01:20:26.866Z |
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