Enantioselective Palladium-Catalyzed [3C + 2C] and [4C + 3C] Intramolecular Cycloadditions of Alkylidenecyclopropanes
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Title: | Enantioselective Palladium-Catalyzed [3C + 2C] and [4C + 3C] Intramolecular Cycloadditions of Alkylidenecyclopropanes |
Author: | Verdugo Leal, Felipe Ignacio Villarino Palmaz, Lara Durán, Juan Gulías Costa, Moisés Mascareñas Cid, José Luis López García, Fernando |
Affiliation: | Universidade de Santiago de Compostela. Centro de Investigación en Química Biolóxica e Materiais Moleculares Universidade de Santiago de Compostela. Departamento de Química Orgánica |
Subject: | Alkylidenecyclopropane | Asymmetric | Cycloaddition | Enantioselective | Palladium | Phosphoramidite | |
Date of Issue: | 2018-06-04 |
Publisher: | American Chemical Society |
Citation: | Verdugo, F., Villarino, L., Durán, J., Gulías, M., Mascareñas, J., & López, F. (2018). Enantioselective Palladium-Catalyzed [3C + 2C] and [4C + 3C] Intramolecular Cycloadditions of Alkylidenecyclopropanes. ACS Catalysis, 8(7), 6100-6105. doi: 10.1021/acscatal.8b01296 |
Abstract: | We report a highly enantioselective [3C + 2C] intramolecular cycloaddition of alkylidenecyclopropanes (ACPs) and alkenes. The best results are obtained by using sterically demanding chiral phosphoramidite ligands derived from Vapol. Moreover, we also show that related, but less bulky, phosphoramidites can also lead to very effective [4C + 3C] cycloadditions when dienes, instead of alkenes, are used as reacting partners. The reactions provide a practical, simple, and selective access to optically active, synthetically appealing 5,5- and 5,7-bicyclic systems |
Description: | NOTICE: This is the peer reviewed version of the following article: Felipe Verdugo, Lara Villarino, Juan Durán, Moisés Gulías, José L. Mascareñas and Fernando López (2018), Enantioselective Palladium-Catalyzed [3C + 2C] and [4C + 3C] Intra-molecular Cycloadditions of Alkylidenecyclopropanes. ACS Catalysis, 2018, 8, 6100–6105 [DOI: 10.1021/acscatal.8b01296]. This article may be used for non-commercial purposes in accordance with American Chemical Society Terms and Conditions for self-archiving |
Publisher version: | https://doi.org/10.1021/acscatal.8b01296 |
URI: | http://hdl.handle.net/10347/17410 |
DOI: | 10.1021/acscatal.8b01296 |
ISSN: | 2155-5435 |
Rights: | © 2018 American Chemical Society |
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