13 research outputs found
ÂżEs capaz el mindfulness de reducir la intensidad de juicio y el efecto de falso consenso?
Treball Final de Grau en Psicologia. Codi: PS1048. Curs acadèmic: 2016/2017El mindfulness es, por definición, la acción de prestar atención completa a la experiencia presente de
una forma particular, con un propĂłsito y sin hacer juicios o evaluaciones de los eventos privados
experimentados y de los estĂmulos externos relacionados con estos eventos privados. Este ejercicio es
una técnica de relajación que, en numerosos estudios, ha demostrado ser capaz de producir efectos
positivos en el ámbito laboral, educativo y sanitario. Sin embargo, es escasa la literatura que explica
los mecanismos cognitivos a los que afecta esta tĂ©cnica y que explicarĂan estos efectos. Algunos de los
estudios que pretenden dar una explicaciĂłn a tales efectos han demostrado que el mindfulness es capaz
de mejorar las capacidades cognitivas y los procesos atencionales. En lo referido a procesos
atributivos, se ha demostrado que algunos de los sesgos atributivos elementales, como el sesgo de
correspondencia, se reducen de forma significativa con la práctica de esta técnica dada la capacidad
para otorgar a sus practicantes la habilidad de realizar observaciones centradas en el momento presente
e impedir en gran medida la actuación de mecanismos automáticos de prejuicio y estereotipación. El
presente estudio pretende conocer en qué medida es capaz el mindfulness de modificar la intensidad
con la que las personas emiten juicios morales, asĂ como a cometer errores atributivos, en concreto el
efecto de falso consenso. Para este cometido se ha contado con una muestra de 440 participantes y se
han utilizado herramientas como el cuestionario MINDSENS, la Escala de Necesidad de CogniciĂłn y
cuestionarios de elaboraciĂłn propia donde los participantes debĂan emitir juicios, considerar el
consenso social existente y situar estas respuestas en una dimensiĂłn de intensidad. Los resultados
obtenidos reflejan una reducciĂłn significativa del efecto de falso consenso en los participantes
meditadores. Sin embargo, no se aprecian diferencias en la intensidad de los juicios emitidos entre
meditadores y no meditadores.Mindfulness is, by definition, the action of paying attention to the actual experience in a particular
way, with a purpose and without making judgments or evaluations of the experienced private events
and the external stimuli related to these private events. This exercise is a relaxation technique that, in
many studies, has shown to be able to produce positive effects in the labor, educational and health
field. However, there are not many literature explaining the cognitive mechanisms that affect this
technique and explain these effects. Some of the studies that attempt to explain the stories have shown
that mindfulness is capable of improving cognitive abilities and attentional processes. With regard to attributive processes, it has been shown that some of the biases of elemental attributions, such as
correspondence bias, are significantly reduced with the practice of this technique given the ability to
give its practitioners the ability to perform observations centered on the present moment and greatly
impede the performance of automatic mechanisms of prejudice and stereotyping. The present study
intends to know to what extent the mindfulness is able to modify the intensity with which people emit
moral judgments, as well as to commit attributive errors, in particular the effect of false consensus. For
this purpose, a sample of 440 participants has used tools such as the MINDSENS questionnaire, the
Cognition Need Scale and the self-elaboration questionnaires where participants should make
judgments, consider the existing social consensus and find these answers in An intensity dimension
The results obtained reflect a significant reduction of the effect of false consensus on the meditator
participants. However, there are no differences in the intensity of the judgments emitted between
meditators and non-meditators
Pd(II)-Catalyzed <i>ortho</i>-C–H Oxidation of Arylacetic Acid Derivatives: Synthesis of Benzofuranones
PdÂ(II)-catalyzed <i>ortho</i>-C–H acetoxylation
of arylacetic acid derivatives is demonstrated with the aid of a novel <i>S</i>-methyl-<i>S</i>-2-pyridylÂsulfoximine (MPyS)
directing group (DG). The α-mono- and α-unsubstituted
arylacetic acid derivatives were readily employed in the <i>ortho</i>-C–H acetoxylations. The oxidation products are hydrolyzed,
and the MPyS-DG is easily recovered, providing ready access to <i>o</i>-hydroxyÂarylacetic acids. 3-Mono- and 3-unsubstituted
benzoÂfuranones are synthesized from <i>o</i>-hydroxyÂarylÂacetic
acids
Pd(II)-Catalyzed Primary-C(sp<sup>3</sup>)–H Acyloxylation at Room Temperature
With the aid of a novel <i>S</i>-methyl-<i>S</i>-2-pyridyl-sulfoximine (MPyS) directing group (DG), the unactivated primary β-C(sp<sup>3</sup>)–H bond of MPyS-<i>N</i>-amides oxidizes at room temperature. The catalytic conditions are applicable to the diacetoxylation of primary β,β′-C(sp<sup>3</sup>)–H bonds, and the carboxylic acid solvent is pivotal in the formation of the C–O bond. The MPyS-DG cleaves from the oxidation products and is recovered. This method provides convenient access to α,α′-disubstituted-β-hydroxycarboxylic acids
Sulfoximine Directed Intermolecular <i>o</i>‑C–H Amidation of Arenes with Sulfonyl Azides
The Ru(II)-catalyzed intermolecular <i>o</i>-C–H amidation of arenes in N-benzoylated sulfoximine with sulfonyl azides is demonstrated. The reaction proceeds with broad substrate scope and tolerates various functional groups. Base hydrolysis of the amidation product provides the anthranilic acid derivatives and methylphenyl sulfoximine (MPS) directing group. This method is successfully employed for the synthesis of HMR 1766
Sulfoximine Directed Intermolecular <i>o</i>‑C–H Amidation of Arenes with Sulfonyl Azides
The Ru(II)-catalyzed intermolecular <i>o</i>-C–H amidation of arenes in N-benzoylated sulfoximine with sulfonyl azides is demonstrated. The reaction proceeds with broad substrate scope and tolerates various functional groups. Base hydrolysis of the amidation product provides the anthranilic acid derivatives and methylphenyl sulfoximine (MPS) directing group. This method is successfully employed for the synthesis of HMR 1766
Ruthenium-Catalyzed Intramolecular Hydroarylation of Arenes and Mechanistic Study: Synthesis of Dihydrobenzofurans, Indolines, and Chromans
A ruthenium-catalyzed,
amide-directed intramolecular hydroarylation
of alkene-tethered benzamide derivatives is discussed. This method
proficiently constructs dihydrobenzofuran, indoline, and chroman skeletons
of biological significance in good to excellent yields; the overall
process is atom-economical and step-efficient. The reaction exhibits
broad scope, tolerating common functional groups, labile protecting
units, and heteroaryl motifs. The use of a catalytic amount of base
suffices the need. Deuterium scrambling and kinetic studies offer
valuable facts for understanding the reaction mechanism
Ruthenium-Catalyzed Intramolecular Hydroarylation of Arenes and Mechanistic Study: Synthesis of Dihydrobenzofurans, Indolines, and Chromans
A ruthenium-catalyzed,
amide-directed intramolecular hydroarylation
of alkene-tethered benzamide derivatives is discussed. This method
proficiently constructs dihydrobenzofuran, indoline, and chroman skeletons
of biological significance in good to excellent yields; the overall
process is atom-economical and step-efficient. The reaction exhibits
broad scope, tolerating common functional groups, labile protecting
units, and heteroaryl motifs. The use of a catalytic amount of base
suffices the need. Deuterium scrambling and kinetic studies offer
valuable facts for understanding the reaction mechanism
Sulfoximine-Directed Ruthenium-Catalyzed <i>ortho</i>-C–H Alkenylation of (Hetero)Arenes: Synthesis of EP3 Receptor Antagonist Analogue
The
reusable sulfoxÂimine directing-group-assisted RuÂ(II)-catalyzed
chemo- and regioÂselective <i>ortho</i>-C–H
alkenylation of arenes and heteroÂarenes with acrylates and α,β-unsaturated
ketones/vinyl sulfone is shown. The <i>N</i>-aroyl sulfoximine
undergoes annulation with diphenylÂacetylene, delivering isoÂquinoliÂnones
and methyl phenyl sulfoxide. The present protocol is successfully
employed for the synthesis of the EP3 receptor antagonist analogue
Ru-Catalyzed One-Pot Diannulation of Heteroaryls: Direct Access to π‑Conjugated Polycyclic Amides
A novel Ru-catalyzed
oxidative double annulation of heteroarenes
with symmetrical and unsymmetrical alkynes is reported. A general
method for the unsymmetrical annulation of heteroarenes with two distinct
alkynes is showcased for the first time. Methylphenyl sulfoximine
(MPS) plays an important role in the annulations of heteroarenes and
allows the construction of structurally complex π-conjugated
heteroarene-fused polycyclic amide skeletons via the formation of
multiple C–C and C–N bonds in a single operation. The
reaction exhibits excellent substrate scope and tolerates a wide range
of functional groups