The promoting effect of pyridine ligands in the Pd-catalysed Heck–Matsuda reaction; New Journal of Chemistry; Vol. 40, iss. 10
| Parent link: | New Journal of Chemistry Vol. 40, iss. 10.— 2016.— [P. 8855-8862] |
|---|---|
| Autor Corporativo: | |
| Outros autores: | , , , , , , , |
| Summary: | Title screen An efficient Pd-catalyzed arylation reaction of challenging acyclic olefins, in the presence of an organic ligand, has been disclosed. Commercially available cheap pyridine-based ligands are able to promote good to excellent yields for poorly efficient Heck–Matsuda arylation reactions of several allylic alcohols. A wide range of electronically different arenediazonium salts bearing either electron-releasing or withdrawing groups have been used allowing the synthesis of a range of Я-aryl-methoxy-lactols. The catalytic system has been optimised, along with the reaction conditions, in order to achieve remarkable yields in less than 1 h. Режим доступа: по договору с организацией-держателем ресурса |
| Idioma: | inglés |
| Publicado: |
2016
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| Subjects: | |
| Acceso en liña: | http://dx.doi.org/10.1039/C6NJ01717G |
| Formato: | Electrónico Capítulo de libro |
| KOHA link: | https://koha.lib.tpu.ru/cgi-bin/koha/opac-detail.pl?biblionumber=650629 |
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| 200 | 1 | |a The promoting effect of pyridine ligands in the Pd-catalysed Heck–Matsuda reaction |f W. Khodja [et al.] | |
| 203 | |a Text |c electronic | ||
| 300 | |a Title screen | ||
| 320 | |a [References: 48 tit.] | ||
| 330 | |a An efficient Pd-catalyzed arylation reaction of challenging acyclic olefins, in the presence of an organic ligand, has been disclosed. Commercially available cheap pyridine-based ligands are able to promote good to excellent yields for poorly efficient Heck–Matsuda arylation reactions of several allylic alcohols. A wide range of electronically different arenediazonium salts bearing either electron-releasing or withdrawing groups have been used allowing the synthesis of a range of Я-aryl-methoxy-lactols. The catalytic system has been optimised, along with the reaction conditions, in order to achieve remarkable yields in less than 1 h. | ||
| 333 | |a Режим доступа: по договору с организацией-держателем ресурса | ||
| 461 | |t New Journal of Chemistry | ||
| 463 | |t Vol. 40, iss. 10 |v [P. 8855-8862] |d 2016 | ||
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| 701 | 1 | |a Zammattio |b F. |g Francoise | |
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