Palladium(II) chalcogenolate complexes as catalysts for CC cross-coupling and carbonylative Suzuki coupling reactions
Abstract The catalytic activity of palladium chalcogenolate complexes, [PdCl(ECH2CH2NMe2)]3 (E=S or Se), [PdCl(ECH2CH2CH2NMe2)]2 and [PdCl(SeCH2CH2NMe2)(PPh3)] has been investigated in carbonylative Suzuki coupling reactions. The phosphine complex has also been used as a catalyst in CC cross couplin...
Ausführliche Beschreibung
Gespeichert in:
| Autor*in: |
Paluru, Dilip K. [verfasserIn] |
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| Format: |
E-Artikel |
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| Sprache: |
Englisch |
| Erschienen: |
2014transfer abstract |
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| Umfang: |
4 |
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| Übergeordnetes Werk: |
Enthalten in: Continuing Medical Education Program - 2013, Amsterdam [u.a.] |
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| Übergeordnetes Werk: |
volume:55 ; year:2014 ; number:18 ; day:30 ; month:04 ; pages:2953-2956 ; extent:4 |
| Links: |
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| DOI / URN: |
10.1016/j.tetlet.2014.03.101 |
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| 245 | 1 | 0 | |a Palladium(II) chalcogenolate complexes as catalysts for CC cross-coupling and carbonylative Suzuki coupling reactions |
| 264 | 1 | |c 2014transfer abstract | |
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| 520 | |a Abstract The catalytic activity of palladium chalcogenolate complexes, [PdCl(ECH2CH2NMe2)]3 (E=S or Se), [PdCl(ECH2CH2CH2NMe2)]2 and [PdCl(SeCH2CH2NMe2)(PPh3)] has been investigated in carbonylative Suzuki coupling reactions. The phosphine complex has also been used as a catalyst in CC cross coupling reactions involving an aryl halide and either triaryl bismuth or aryl boronic acid (Suzuki coupling). The catalytic system was also explored for other carbonylation reactions including carbonylative Sonogashira coupling and amino carbonylation reaction. The phosphine complex showed better activity in carbonylative Suzuki coupling reactions than dimeric and trimeric complexes. All the complexes showed comparable activity in Suzuki coupling reactions. | ||
| 520 | |a Abstract The catalytic activity of palladium chalcogenolate complexes, [PdCl(ECH2CH2NMe2)]3 (E=S or Se), [PdCl(ECH2CH2CH2NMe2)]2 and [PdCl(SeCH2CH2NMe2)(PPh3)] has been investigated in carbonylative Suzuki coupling reactions. The phosphine complex has also been used as a catalyst in CC cross coupling reactions involving an aryl halide and either triaryl bismuth or aryl boronic acid (Suzuki coupling). The catalytic system was also explored for other carbonylation reactions including carbonylative Sonogashira coupling and amino carbonylation reaction. The phosphine complex showed better activity in carbonylative Suzuki coupling reactions than dimeric and trimeric complexes. All the complexes showed comparable activity in Suzuki coupling reactions. | ||
| 650 | 7 | |a Suzuki coupling |2 Elsevier | |
| 650 | 7 | |a Chalcogenolate |2 Elsevier | |
| 650 | 7 | |a Palladium |2 Elsevier | |
| 650 | 7 | |a Carbonylative Suzuki coupling |2 Elsevier | |
| 650 | 7 | |a Triarylbismuth |2 Elsevier | |
| 700 | 1 | |a Dey, Sandip |4 oth | |
| 700 | 1 | |a Chaudhari, Kamal R. |4 oth | |
| 700 | 1 | |a Khedkar, Mayur V. |4 oth | |
| 700 | 1 | |a Bhanage, Bhalachandra M. |4 oth | |
| 700 | 1 | |a Jain, Vimal K. |4 oth | |
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10.1016/j.tetlet.2014.03.101 doi GBVA2014001000018.pica (DE-627)ELV022374922 (ELSEVIER)S0040-4039(14)00522-X DE-627 ger DE-627 rakwb eng 540 540 DE-600 610 VZ 540 VZ 35.00 bkl Paluru, Dilip K. verfasserin aut Palladium(II) chalcogenolate complexes as catalysts for CC cross-coupling and carbonylative Suzuki coupling reactions 2014transfer abstract 4 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Abstract The catalytic activity of palladium chalcogenolate complexes, [PdCl(ECH2CH2NMe2)]3 (E=S or Se), [PdCl(ECH2CH2CH2NMe2)]2 and [PdCl(SeCH2CH2NMe2)(PPh3)] has been investigated in carbonylative Suzuki coupling reactions. The phosphine complex has also been used as a catalyst in CC cross coupling reactions involving an aryl halide and either triaryl bismuth or aryl boronic acid (Suzuki coupling). The catalytic system was also explored for other carbonylation reactions including carbonylative Sonogashira coupling and amino carbonylation reaction. The phosphine complex showed better activity in carbonylative Suzuki coupling reactions than dimeric and trimeric complexes. All the complexes showed comparable activity in Suzuki coupling reactions. Abstract The catalytic activity of palladium chalcogenolate complexes, [PdCl(ECH2CH2NMe2)]3 (E=S or Se), [PdCl(ECH2CH2CH2NMe2)]2 and [PdCl(SeCH2CH2NMe2)(PPh3)] has been investigated in carbonylative Suzuki coupling reactions. The phosphine complex has also been used as a catalyst in CC cross coupling reactions involving an aryl halide and either triaryl bismuth or aryl boronic acid (Suzuki coupling). The catalytic system was also explored for other carbonylation reactions including carbonylative Sonogashira coupling and amino carbonylation reaction. The phosphine complex showed better activity in carbonylative Suzuki coupling reactions than dimeric and trimeric complexes. All the complexes showed comparable activity in Suzuki coupling reactions. Suzuki coupling Elsevier Chalcogenolate Elsevier Palladium Elsevier Carbonylative Suzuki coupling Elsevier Triarylbismuth Elsevier Dey, Sandip oth Chaudhari, Kamal R. oth Khedkar, Mayur V. oth Bhanage, Bhalachandra M. oth Jain, Vimal K. oth Enthalten in Elsevier Science Continuing Medical Education Program 2013 Amsterdam [u.a.] (DE-627)ELV011942339 volume:55 year:2014 number:18 day:30 month:04 pages:2953-2956 extent:4 https://doi.org/10.1016/j.tetlet.2014.03.101 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U SSG-OLC-PHA 35.00 Chemie: Allgemeines VZ AR 55 2014 18 30 0430 2953-2956 4 045F 540 |
| spelling |
10.1016/j.tetlet.2014.03.101 doi GBVA2014001000018.pica (DE-627)ELV022374922 (ELSEVIER)S0040-4039(14)00522-X DE-627 ger DE-627 rakwb eng 540 540 DE-600 610 VZ 540 VZ 35.00 bkl Paluru, Dilip K. verfasserin aut Palladium(II) chalcogenolate complexes as catalysts for CC cross-coupling and carbonylative Suzuki coupling reactions 2014transfer abstract 4 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Abstract The catalytic activity of palladium chalcogenolate complexes, [PdCl(ECH2CH2NMe2)]3 (E=S or Se), [PdCl(ECH2CH2CH2NMe2)]2 and [PdCl(SeCH2CH2NMe2)(PPh3)] has been investigated in carbonylative Suzuki coupling reactions. The phosphine complex has also been used as a catalyst in CC cross coupling reactions involving an aryl halide and either triaryl bismuth or aryl boronic acid (Suzuki coupling). The catalytic system was also explored for other carbonylation reactions including carbonylative Sonogashira coupling and amino carbonylation reaction. The phosphine complex showed better activity in carbonylative Suzuki coupling reactions than dimeric and trimeric complexes. All the complexes showed comparable activity in Suzuki coupling reactions. Abstract The catalytic activity of palladium chalcogenolate complexes, [PdCl(ECH2CH2NMe2)]3 (E=S or Se), [PdCl(ECH2CH2CH2NMe2)]2 and [PdCl(SeCH2CH2NMe2)(PPh3)] has been investigated in carbonylative Suzuki coupling reactions. The phosphine complex has also been used as a catalyst in CC cross coupling reactions involving an aryl halide and either triaryl bismuth or aryl boronic acid (Suzuki coupling). The catalytic system was also explored for other carbonylation reactions including carbonylative Sonogashira coupling and amino carbonylation reaction. The phosphine complex showed better activity in carbonylative Suzuki coupling reactions than dimeric and trimeric complexes. All the complexes showed comparable activity in Suzuki coupling reactions. Suzuki coupling Elsevier Chalcogenolate Elsevier Palladium Elsevier Carbonylative Suzuki coupling Elsevier Triarylbismuth Elsevier Dey, Sandip oth Chaudhari, Kamal R. oth Khedkar, Mayur V. oth Bhanage, Bhalachandra M. oth Jain, Vimal K. oth Enthalten in Elsevier Science Continuing Medical Education Program 2013 Amsterdam [u.a.] (DE-627)ELV011942339 volume:55 year:2014 number:18 day:30 month:04 pages:2953-2956 extent:4 https://doi.org/10.1016/j.tetlet.2014.03.101 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U SSG-OLC-PHA 35.00 Chemie: Allgemeines VZ AR 55 2014 18 30 0430 2953-2956 4 045F 540 |
| allfields_unstemmed |
10.1016/j.tetlet.2014.03.101 doi GBVA2014001000018.pica (DE-627)ELV022374922 (ELSEVIER)S0040-4039(14)00522-X DE-627 ger DE-627 rakwb eng 540 540 DE-600 610 VZ 540 VZ 35.00 bkl Paluru, Dilip K. verfasserin aut Palladium(II) chalcogenolate complexes as catalysts for CC cross-coupling and carbonylative Suzuki coupling reactions 2014transfer abstract 4 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Abstract The catalytic activity of palladium chalcogenolate complexes, [PdCl(ECH2CH2NMe2)]3 (E=S or Se), [PdCl(ECH2CH2CH2NMe2)]2 and [PdCl(SeCH2CH2NMe2)(PPh3)] has been investigated in carbonylative Suzuki coupling reactions. The phosphine complex has also been used as a catalyst in CC cross coupling reactions involving an aryl halide and either triaryl bismuth or aryl boronic acid (Suzuki coupling). The catalytic system was also explored for other carbonylation reactions including carbonylative Sonogashira coupling and amino carbonylation reaction. The phosphine complex showed better activity in carbonylative Suzuki coupling reactions than dimeric and trimeric complexes. All the complexes showed comparable activity in Suzuki coupling reactions. Abstract The catalytic activity of palladium chalcogenolate complexes, [PdCl(ECH2CH2NMe2)]3 (E=S or Se), [PdCl(ECH2CH2CH2NMe2)]2 and [PdCl(SeCH2CH2NMe2)(PPh3)] has been investigated in carbonylative Suzuki coupling reactions. The phosphine complex has also been used as a catalyst in CC cross coupling reactions involving an aryl halide and either triaryl bismuth or aryl boronic acid (Suzuki coupling). The catalytic system was also explored for other carbonylation reactions including carbonylative Sonogashira coupling and amino carbonylation reaction. The phosphine complex showed better activity in carbonylative Suzuki coupling reactions than dimeric and trimeric complexes. All the complexes showed comparable activity in Suzuki coupling reactions. Suzuki coupling Elsevier Chalcogenolate Elsevier Palladium Elsevier Carbonylative Suzuki coupling Elsevier Triarylbismuth Elsevier Dey, Sandip oth Chaudhari, Kamal R. oth Khedkar, Mayur V. oth Bhanage, Bhalachandra M. oth Jain, Vimal K. oth Enthalten in Elsevier Science Continuing Medical Education Program 2013 Amsterdam [u.a.] (DE-627)ELV011942339 volume:55 year:2014 number:18 day:30 month:04 pages:2953-2956 extent:4 https://doi.org/10.1016/j.tetlet.2014.03.101 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U SSG-OLC-PHA 35.00 Chemie: Allgemeines VZ AR 55 2014 18 30 0430 2953-2956 4 045F 540 |
| allfieldsGer |
10.1016/j.tetlet.2014.03.101 doi GBVA2014001000018.pica (DE-627)ELV022374922 (ELSEVIER)S0040-4039(14)00522-X DE-627 ger DE-627 rakwb eng 540 540 DE-600 610 VZ 540 VZ 35.00 bkl Paluru, Dilip K. verfasserin aut Palladium(II) chalcogenolate complexes as catalysts for CC cross-coupling and carbonylative Suzuki coupling reactions 2014transfer abstract 4 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Abstract The catalytic activity of palladium chalcogenolate complexes, [PdCl(ECH2CH2NMe2)]3 (E=S or Se), [PdCl(ECH2CH2CH2NMe2)]2 and [PdCl(SeCH2CH2NMe2)(PPh3)] has been investigated in carbonylative Suzuki coupling reactions. The phosphine complex has also been used as a catalyst in CC cross coupling reactions involving an aryl halide and either triaryl bismuth or aryl boronic acid (Suzuki coupling). The catalytic system was also explored for other carbonylation reactions including carbonylative Sonogashira coupling and amino carbonylation reaction. The phosphine complex showed better activity in carbonylative Suzuki coupling reactions than dimeric and trimeric complexes. All the complexes showed comparable activity in Suzuki coupling reactions. Abstract The catalytic activity of palladium chalcogenolate complexes, [PdCl(ECH2CH2NMe2)]3 (E=S or Se), [PdCl(ECH2CH2CH2NMe2)]2 and [PdCl(SeCH2CH2NMe2)(PPh3)] has been investigated in carbonylative Suzuki coupling reactions. The phosphine complex has also been used as a catalyst in CC cross coupling reactions involving an aryl halide and either triaryl bismuth or aryl boronic acid (Suzuki coupling). The catalytic system was also explored for other carbonylation reactions including carbonylative Sonogashira coupling and amino carbonylation reaction. The phosphine complex showed better activity in carbonylative Suzuki coupling reactions than dimeric and trimeric complexes. All the complexes showed comparable activity in Suzuki coupling reactions. Suzuki coupling Elsevier Chalcogenolate Elsevier Palladium Elsevier Carbonylative Suzuki coupling Elsevier Triarylbismuth Elsevier Dey, Sandip oth Chaudhari, Kamal R. oth Khedkar, Mayur V. oth Bhanage, Bhalachandra M. oth Jain, Vimal K. oth Enthalten in Elsevier Science Continuing Medical Education Program 2013 Amsterdam [u.a.] (DE-627)ELV011942339 volume:55 year:2014 number:18 day:30 month:04 pages:2953-2956 extent:4 https://doi.org/10.1016/j.tetlet.2014.03.101 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U SSG-OLC-PHA 35.00 Chemie: Allgemeines VZ AR 55 2014 18 30 0430 2953-2956 4 045F 540 |
| allfieldsSound |
10.1016/j.tetlet.2014.03.101 doi GBVA2014001000018.pica (DE-627)ELV022374922 (ELSEVIER)S0040-4039(14)00522-X DE-627 ger DE-627 rakwb eng 540 540 DE-600 610 VZ 540 VZ 35.00 bkl Paluru, Dilip K. verfasserin aut Palladium(II) chalcogenolate complexes as catalysts for CC cross-coupling and carbonylative Suzuki coupling reactions 2014transfer abstract 4 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Abstract The catalytic activity of palladium chalcogenolate complexes, [PdCl(ECH2CH2NMe2)]3 (E=S or Se), [PdCl(ECH2CH2CH2NMe2)]2 and [PdCl(SeCH2CH2NMe2)(PPh3)] has been investigated in carbonylative Suzuki coupling reactions. The phosphine complex has also been used as a catalyst in CC cross coupling reactions involving an aryl halide and either triaryl bismuth or aryl boronic acid (Suzuki coupling). The catalytic system was also explored for other carbonylation reactions including carbonylative Sonogashira coupling and amino carbonylation reaction. The phosphine complex showed better activity in carbonylative Suzuki coupling reactions than dimeric and trimeric complexes. All the complexes showed comparable activity in Suzuki coupling reactions. Abstract The catalytic activity of palladium chalcogenolate complexes, [PdCl(ECH2CH2NMe2)]3 (E=S or Se), [PdCl(ECH2CH2CH2NMe2)]2 and [PdCl(SeCH2CH2NMe2)(PPh3)] has been investigated in carbonylative Suzuki coupling reactions. The phosphine complex has also been used as a catalyst in CC cross coupling reactions involving an aryl halide and either triaryl bismuth or aryl boronic acid (Suzuki coupling). The catalytic system was also explored for other carbonylation reactions including carbonylative Sonogashira coupling and amino carbonylation reaction. The phosphine complex showed better activity in carbonylative Suzuki coupling reactions than dimeric and trimeric complexes. All the complexes showed comparable activity in Suzuki coupling reactions. Suzuki coupling Elsevier Chalcogenolate Elsevier Palladium Elsevier Carbonylative Suzuki coupling Elsevier Triarylbismuth Elsevier Dey, Sandip oth Chaudhari, Kamal R. oth Khedkar, Mayur V. oth Bhanage, Bhalachandra M. oth Jain, Vimal K. oth Enthalten in Elsevier Science Continuing Medical Education Program 2013 Amsterdam [u.a.] (DE-627)ELV011942339 volume:55 year:2014 number:18 day:30 month:04 pages:2953-2956 extent:4 https://doi.org/10.1016/j.tetlet.2014.03.101 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U SSG-OLC-PHA 35.00 Chemie: Allgemeines VZ AR 55 2014 18 30 0430 2953-2956 4 045F 540 |
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Enthalten in Continuing Medical Education Program Amsterdam [u.a.] volume:55 year:2014 number:18 day:30 month:04 pages:2953-2956 extent:4 |
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Paluru, Dilip K. @@aut@@ Dey, Sandip @@oth@@ Chaudhari, Kamal R. @@oth@@ Khedkar, Mayur V. @@oth@@ Bhanage, Bhalachandra M. @@oth@@ Jain, Vimal K. @@oth@@ |
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Palladium(II) chalcogenolate complexes as catalysts for CC cross-coupling and carbonylative Suzuki coupling reactions |
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Abstract The catalytic activity of palladium chalcogenolate complexes, [PdCl(ECH2CH2NMe2)]3 (E=S or Se), [PdCl(ECH2CH2CH2NMe2)]2 and [PdCl(SeCH2CH2NMe2)(PPh3)] has been investigated in carbonylative Suzuki coupling reactions. The phosphine complex has also been used as a catalyst in CC cross coupling reactions involving an aryl halide and either triaryl bismuth or aryl boronic acid (Suzuki coupling). The catalytic system was also explored for other carbonylation reactions including carbonylative Sonogashira coupling and amino carbonylation reaction. The phosphine complex showed better activity in carbonylative Suzuki coupling reactions than dimeric and trimeric complexes. All the complexes showed comparable activity in Suzuki coupling reactions. |
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Abstract The catalytic activity of palladium chalcogenolate complexes, [PdCl(ECH2CH2NMe2)]3 (E=S or Se), [PdCl(ECH2CH2CH2NMe2)]2 and [PdCl(SeCH2CH2NMe2)(PPh3)] has been investigated in carbonylative Suzuki coupling reactions. The phosphine complex has also been used as a catalyst in CC cross coupling reactions involving an aryl halide and either triaryl bismuth or aryl boronic acid (Suzuki coupling). The catalytic system was also explored for other carbonylation reactions including carbonylative Sonogashira coupling and amino carbonylation reaction. The phosphine complex showed better activity in carbonylative Suzuki coupling reactions than dimeric and trimeric complexes. All the complexes showed comparable activity in Suzuki coupling reactions. |
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Abstract The catalytic activity of palladium chalcogenolate complexes, [PdCl(ECH2CH2NMe2)]3 (E=S or Se), [PdCl(ECH2CH2CH2NMe2)]2 and [PdCl(SeCH2CH2NMe2)(PPh3)] has been investigated in carbonylative Suzuki coupling reactions. The phosphine complex has also been used as a catalyst in CC cross coupling reactions involving an aryl halide and either triaryl bismuth or aryl boronic acid (Suzuki coupling). The catalytic system was also explored for other carbonylation reactions including carbonylative Sonogashira coupling and amino carbonylation reaction. The phosphine complex showed better activity in carbonylative Suzuki coupling reactions than dimeric and trimeric complexes. All the complexes showed comparable activity in Suzuki coupling reactions. |
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