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1.
BMC Med Res Methodol ; 20(1): 25, 2020 02 07.
Artigo em Inglês | MEDLINE | ID: mdl-32028894

RESUMO

BACKGROUND: We recently developed CoCites, a citation-based search method that is designed to be more efficient than traditional keyword-based methods. The method begins with identification of one or more highly relevant publications (query articles) and consists of two searches: the co-citation search, which ranks publications on their co-citation frequency with the query articles, and the citation search, which ranks publications on frequency of all citations that cite or are cited by the query articles. METHODS: We aimed to reproduce the literature searches of published systematic reviews and meta-analyses and assess whether CoCites retrieves all eligible articles while screening fewer titles. RESULTS: A total of 250 reviews were included. CoCites retrieved a median of 75% of the articles that were included in the original reviews. The percentage of retrieved articles was higher (88%) when the query articles were cited more frequently and when they had more overlap in their citations. Applying CoCites to only the highest-cited article yielded similar results. The co-citation and citation searches combined were more efficient when the review authors had screened more than 500 titles, but not when they had screened less. CONCLUSIONS: CoCites is an efficient and accurate method for finding relevant related articles. The method uses the expert knowledge of authors to rank related articles, does not depend on keyword selection and requires no special expertise to build search queries. The method is transparent and reproducible.


Assuntos
Armazenamento e Recuperação da Informação/métodos , Modelos Teóricos , Publicações/estatística & dados numéricos , Projetos de Pesquisa/estatística & dados numéricos , Humanos , Fator de Impacto de Revistas , Reprodutibilidade dos Testes
2.
J Org Chem ; 79(20): 9728-34, 2014 Oct 17.
Artigo em Inglês | MEDLINE | ID: mdl-25279826

RESUMO

Rh(II)-catalyzed oxonium ylide formation-[2,3] sigmatropic rearrangement of α-diazo-ß-ketoesters possessing γ-cyclic unsaturated acetal substitution, followed by acid-catalyzed elimination-lactonization, provides a concise approach to 1,7-dioxaspiro[4.4]non-2-ene-4,6-diones. The process creates adjacent quaternary stereocenters with full control of the relative stereochemistry. An unsymmetrical monomethylated cyclic unsaturated acetal leads to hyperolactone C, where ylide formation-rearrangement proceeds with high selectivity between subtly nonequivalent acetal oxygen atoms.


Assuntos
Acetais/química , Furanos/síntese química , Oniocompostos/química , Ródio/química , Compostos de Espiro/química , Furanos/química , Estrutura Molecular , Estereoisomerismo
3.
Org Lett ; 16(8): 2158-61, 2014 Apr 18.
Artigo em Inglês | MEDLINE | ID: mdl-24673520

RESUMO

A palladium-catalyzed cyanation of alkenyl halides using acetone cyanohydrin is described. A number of structurally diverse alkenylic nitrile containing compounds was prepared in one step under optimized conditions. The reaction proved to be efficient, chemoselective, easy to perform, and tolerant of a number of functional groups.


Assuntos
Alcenos/química , Alcenos/síntese química , Hidrocarbonetos Bromados/síntese química , Nitrilas/química , Nitrilas/síntese química , Paládio/química , Catálise , Técnicas de Química Combinatória , Hidrocarbonetos Bromados/química , Estrutura Molecular
4.
Phys Chem Chem Phys ; 14(42): 14489-91, 2012 Nov 14.
Artigo em Inglês | MEDLINE | ID: mdl-23032190

RESUMO

The sacoglossan mollusc-derived metabolite, tridachiahydropyrone (3), and its proposed biosynthetic precursors (1 and 2) form part of a complex chemical defence system against predators and harmful UV light. Here, we provide supporting biophysical evidence that the metabolites become selectively localised at cell membranes and outline a binding scheme that accommodates the observed data. The possibility that localised lipid domains within the membrane have an effect on the localisation is also addressed.


Assuntos
Produtos Biológicos/química , Bicamadas Lipídicas/química , Fosfolipídeos/química , Pironas/química , Produtos Biológicos/metabolismo , Bicamadas Lipídicas/metabolismo , Estrutura Molecular , Fosfolipídeos/metabolismo , Pironas/metabolismo , Raios Ultravioleta
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