Synthesis of Pulvinic Acid and Norbadione A Analogues by Suzuki–Miyaura Cross-Coupling of Benzylated Intermediates
Autor: | Charles Mioskowski, Thierry Le Gall, Marine Desage-El Murr, Stéphanie Nowaczyk |
---|---|
Přispěvatelé: | Institut Gilbert-Laustriat : Biomolécules, Biotechnologie, Innovation Thérapeutique, Université Louis Pasteur - Strasbourg I-Centre National de la Recherche Scientifique (CNRS), Klotz, Evelyne |
Rok vydání: | 2006 |
Předmět: | |
Zdroj: | European Journal of Organic Chemistry European Journal of Organic Chemistry, Wiley-VCH Verlag, 2006, 6, pp.1489-1498 |
ISSN: | 1099-0690 1434-193X |
Popis: | Pulvinic acid and norbadione A analogues can be prepared by Suzuki–Miyaura cross-coupling of functionalized arylboronic esters with appropriate vinyl triflates, in which the hydroxy functions are protected either with methyl or benzyl groups, the latter being cleaved in a more reliable fashion at the end of the synthetic sequence. (© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2006) |
Databáze: | OpenAIRE |
Externí odkaz: |