O consumo colaborativo como alternativa ao consumo de massa: a percepção do consumidor em bairros de Florianópolis e a relação do consumo colaborativo com valores pessoais.

TCC (graduação) - Universidade Federal de Santa Catarina. Centro Sócio-Econômico. Economia.O tipo de consumo que a sociedade habituou-se ao longo das últimas décadas tem ocasionado problemas que impactam diretamente o cotidiano das pessoas. Alavancado por motivações individuais e questões ambientais, sociais e econômicas, o consumo colaborativo é um fenômeno recente que vem alterando o funcionamento da economia global ao proporcionar aos consumidores uma nova forma de acomodar seus desejos e necessidades de maneira conveniente e sustentável. Associado a isso, as redes de informação energizadas pela Internet têm modificado significativamente o modo e a velocidade com que os agentes econômicos se relacionam. Nesse sentido, o objetivo maior deste trabalho de conclusão do Curso de Ciências Econômicas é identificar a percepção dos consumidores da Grande Florianópolis acerca do consumo colaborativo como alternativa ao modelo de consumo tradicional. O estudo é dividido em três partes principais. Inicialmente recorre-se a pesquisa bibliográfica para contextualizar e conceituar os termos economia compartilhada e consumo colaborativo, suas formas e princípios. Visando conhecer os efeitos desse movimento no Brasil e especificamente em Florianópolis, na sequencia realiza-se pesquisa através de questionários para identificar a propensão do consumidor a participar de práticas de consumo colaborativo em quatro regiões: Lagoa da Conceição, Centro, Trindade e Continente. Considerando que os valores pessoais interferem no comportamento do consumidor, busca-se avaliar qualitativamente de que forma tais valores se relacionam com a disposição dos mesmos a participar do consumo colaborativo. Através do questionário aplicado, ainda que com amostra limitada, observa-se que os consumidores apresentam de modo geral nível satisfatório de propensão a participar do consumo colaborativo, sendo a Lagoa da Conceição a localidade com maior adesão, seguida por Continente, Trindade e Centro. Além disso, a mensuração dos valores pessoais permite observar que os consumidores mais abertos a mudança, menos conservadores e menos apegados materialmente apresentam maior propensão a participar do consumo colaborativo, como é o caso da Lagoa da Conceição. As considerações finais discutem os principais achados e limitações do estudo

Mediterranean-type diet and brain structural change from 73 to 76 years in a Scottish cohort

STUDY FUNDING The data were collected by a Research into Ageing programme grant; research continues as part of the Age UK–funded Disconnected Mind project. The work was undertaken by The University of Edinburgh Centre for Cognitive Ageing and Cognitive Epidemiology, part of the cross-council Lifelong Health and Wellbeing Initiative (MR/K026992/1), with funding from the BBSRC and Medical Research Council. Imaging and image analysis was performed at the Brain Research Imaging Centre (sbirc.ed.ac.uk/), Edinburgh, supported by the Scottish Funding Council SINAPSE Collaboration. Derivation of mean cortical thickness measures was funded by the Scottish Funding Council’s Postdoctoral and Early Career Researchers Exchange Fund awarded by SINAPSE to David Alexander Dickie. L.C.A.C. acknowledges funding from the Scottish Government's Rural and Environment Science and Analytical Services (RESAS) division.Peer reviewedPublisher PD

Sequential Ruthenium Catalysis for Olefin Isomerization and Oxidation: Application to the Synthesis of Unusual Amino Acids

How can you use a ruthenium isomerization catalyst twice? A ruthenium-catalyzed sequence for the formal two-carbon scission of allyl groups to carboxylic acids has been developed. The reaction includes an initial isomerization step using commercially available ruthenium catalysts followed by <i>in situ</i> transformation of the complex to a metal-oxo species, which is capable of catalyzing subsequent oxidation reactions. The method enables enantioselective syntheses of challenging α-tri- and tetrasubstituted α-amino acids including an expedient total synthesis of the antiepileptic drug levetiracetam

Enantioselective Total Synthesis of (−)-Hunterine A Enabled by a Desymmetrization/Rearrangement Strategy

The first enantioselective total synthesis of (−)-hunterine A is disclosed. Our strategy employs a catalytic asymmetric desymmetrization of a symmetrical diketone and subsequent Beckmann rearrangement to construct a 5,6-α-aminoketone. A convergent 1,2-addition joins a vinyl dianion nucleophile and the enantioenriched ketone. The endgame of the synthesis features an aza-Cope/Mannich reaction and azide-olefin dipolar cycloaddition to complete the pentacyclic ring system. The synthesis is completed through a regioselective aziridine ring opening

Sequential Ruthenium Catalysis for Olefin Isomerization and Oxidation: Application to the Synthesis of Unusual Amino Acids

How can you use a ruthenium isomerization catalyst twice? A ruthenium-catalyzed sequence for the formal two-carbon scission of allyl groups to carboxylic acids has been developed. The reaction includes an initial isomerization step using commercially available ruthenium catalysts followed by <i>in situ</i> transformation of the complex to a metal-oxo species, which is capable of catalyzing subsequent oxidation reactions. The method enables enantioselective syntheses of challenging α-tri- and tetrasubstituted α-amino acids including an expedient total synthesis of the antiepileptic drug levetiracetam

Catalytic Enantioselective Synthesis of Acyclic Quaternary Centers: Palladium-Catalyzed Decarboxylative Allylic Alkylation of Fully Substituted Acyclic Enol Carbonates

The first enantioselective palladium-catalyzed decarboxylative allylic alkylation of fully substituted acyclic enol carbonates providing linear α-quaternary ketones is reported. Investigation into the reaction revealed that the use of an electron-deficient phosphinooxazoline ligand renders the enolate geometry of the starting material inconsequential, with the same enantiomer of product obtained in the same level of selectivity regardless of the starting ratio of enolates. As a result, a general method toward acyclic all-carbon quaternary stereocenters has been developed

Enantio‑, Diastereo‑, and Regioselective Iridium-Catalyzed Asymmetric Allylic Alkylation of Acyclic β‑Ketoesters

The first regio-, diastereo-, and enantioselective allylic alkylation of acyclic β-ketoesters to form vicinal tertiary and all-carbon quaternary stereocenters is reported. Critical to the successful development of this method was the employment of iridium catalysis in concert with <i>N</i>-aryl-phosphoramidite ligands. Broad functional group tolerance is observed at the keto-, ester-, and α-positions of the nucleophile. Various transformations demonstrating the utility of this method for rapidly accessing complex enantioenriched compounds are reported

Development of (Trimethylsilyl)ethyl Ester Protected Enolates and Applications in Palladium-Catalyzed Enantioselective Allylic Alkylation: Intermolecular Cross-Coupling of Functionalized Electrophiles

The development of (trimethylsilyl)­ethyl ester protected enolates is reported. The application of this class of compounds in palladium-catalyzed asymmetric allylic alkylation is explored, yielding a variety of α-quaternary six- and seven-membered ketones and lactams. Independent coupling partner synthesis engenders enhanced allyl substrate scope relative to traditional β-ketoester substrates; highly functionalized α-quaternary ketones generated by the union of (trimethylsilyl)­ethyl β-ketoesters and sensitive allylic alkylation coupling partners serve to demonstrate the utility of this method for complex fragment coupling

Catalytic Enantioselective Synthesis of Acyclic Quaternary Centers: Palladium-Catalyzed Decarboxylative Allylic Alkylation of Fully Substituted Acyclic Enol Carbonates

The first enantioselective palladium-catalyzed decarboxylative allylic alkylation of fully substituted acyclic enol carbonates providing linear α-quaternary ketones is reported. Investigation into the reaction revealed that the use of an electron-deficient phosphinooxazoline ligand renders the enolate geometry of the starting material inconsequential, with the same enantiomer of product obtained in the same level of selectivity regardless of the starting ratio of enolates. As a result, a general method toward acyclic all-carbon quaternary stereocenters has been developed

Enantio‑, Diastereo‑, and Regioselective Iridium-Catalyzed Asymmetric Allylic Alkylation of Acyclic β‑Ketoesters

The first regio-, diastereo-, and enantioselective allylic alkylation of acyclic β-ketoesters to form vicinal tertiary and all-carbon quaternary stereocenters is reported. Critical to the successful development of this method was the employment of iridium catalysis in concert with <i>N</i>-aryl-phosphoramidite ligands. Broad functional group tolerance is observed at the keto-, ester-, and α-positions of the nucleophile. Various transformations demonstrating the utility of this method for rapidly accessing complex enantioenriched compounds are reported