Blay, G.; Fernandez, I.; Monje, B.; Muñoz Roca, MDC.; Pedro, JR.; Vila, C. (2006). Enantioselective synthesis of 2-substituted-1,4-diketones from (S)-mandelic acid enolate and alpha, beta-enones. Tetrahedron. 62(39):9174-9182. https://doi.org/10.1016/j.tet.2006.07.036
Por favor, use este identificador para citar o enlazar este ítem: http://hdl.handle.net/10251/151882
Title: | Enantioselective synthesis of 2-substituted-1,4-diketones from (S)-mandelic acid enolate and alpha, beta-enones | |
Author: | Blay, Gonzalo Fernandez, Isabel Monje, Belen Pedro, Jose R. Vila, Carlos | |
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[EN] An approach for the synthesis of chiral non-racemic 2-substituted-1,4-diketones from (S)-mandelic acid and ¿,ß-enones has been developed. The reaction of lithium enolate of the 1,3-dioxolan-4-one derived from optically ...[+]
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Copyrigths: | Cerrado | |
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Publisher version: | https://doi.org/10.1016/j.tet.2006.07.036 | |
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