Arenediazonium Tosylates (ADTs) as Efficient Reagents for Suzuki–Miyaura Cross-Coupling in Neat Water
| Parent link: | Synthesis: international full-paper journal.— , 1969- Vol. 49, iss. 07.— 2017.— [P. 1680-1688] |
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| Συλλογικό Έργο: | , |
| Άλλοι συγγραφείς: | , , , , , |
| Περίληψη: | Title screen A simple, convenient, and environment-friendly procedure for the preparation of substituted biaryls via Suzuki–Miyaura cross-coupling was developed. The use of arenediazonium tosylates and corresponding boron compounds allows a conversion in neat water in the presence of commercially available Pd(OAc)2 under mild conditions with tolerance to a wide range of functional groups. A procedure particularly useful for the synthesis of di-ortho-substituted biaryls was developed. Режим доступа: по договору с организацией-держателем ресурса |
| Έκδοση: |
2017
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| Θέματα: | |
| Διαθέσιμο Online: | http://dx.doi.org/10.1055/s-0036-1588919 |
| Μορφή: | Ηλεκτρονική πηγή Κεφάλαιο βιβλίου |
| KOHA link: | https://koha.lib.tpu.ru/cgi-bin/koha/opac-detail.pl?biblionumber=653958 |
| Περίληψη: | Title screen A simple, convenient, and environment-friendly procedure for the preparation of substituted biaryls via Suzuki–Miyaura cross-coupling was developed. The use of arenediazonium tosylates and corresponding boron compounds allows a conversion in neat water in the presence of commercially available Pd(OAc)2 under mild conditions with tolerance to a wide range of functional groups. A procedure particularly useful for the synthesis of di-ortho-substituted biaryls was developed. Режим доступа: по договору с организацией-держателем ресурса |
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| DOI: | 10.1055/s-0036-1588919 |