Vila, C.; Quintero, L.; Blay, G.; Muñoz Roca, MDC.; Pedro, J. (2016). Organocatalytic Enantioselective Synthesis of alpha-Hydroxyketones through a Friedel-Crafts Reaction of Naphthols and Activated Phenols with Aryl- and Alkylglyoxal Hydrates. Organic Letters. 18(21):5652-5655. https://doi.org/10.1021/acs.orglett.6b02893
Por favor, use este identificador para citar o enlazar este ítem: http://hdl.handle.net/10251/150297
Title: | Organocatalytic Enantioselective Synthesis of alpha-Hydroxyketones through a Friedel-Crafts Reaction of Naphthols and Activated Phenols with Aryl- and Alkylglyoxal Hydrates | |
Author: | Vila, C. Quintero, L. Blay, G. Pedro, J.R. | |
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[EN] An efficient organocatalytic asymmetric synthesis of alpha-hydroxyketones has been developed. Quinine-derived thiourea catalyzed the enantioselective Friedel Crafts alkylation of naphthols and activated phenols with ...[+]
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Copyrigths: | Cerrado | |
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Publisher version: | https://doi.org/10.1021/acs.orglett.6b02893 | |
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Financial support from the MINECO (Gobierno de Espana; CTQ2013-47494-P) is gratefully acknowledged. C.V. thanks MINECO for a JdC contract. Access to NMR, MS, and X-ray facilities from the Servei Central de Suport a la ...[+]
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