The Nobel Prize In Chemistry 2016: Molecular Machines

The Nobel Prize in Chemistry 2016 was granted to Jean-Pierre Sauvage, Sir James F. Stoddart and Bernard (Ben) L. Feringa. These scientists were responsible for the creation and development of molecular machines. The development of such systems represents a breakthrough in the field of supramolecular chemistry, nanotechnology and organic synthesis. This article aims to bring simple and objective information to the scientific community about the work of these three researchers.40111312

The Nobel Prize in Chemistry 2016: molecular machines

The Nobel Prize in Chemistry 2016 was granted to Jean-Pierre Sauvage, Sir James F. Stoddart and Bernard (Ben) L. Feringa. These scientists were responsible for the creation and development of molecular machines. The development of such systems represents a breakthrough in the field of supramolecular chemistry, nanotechnology and organic synthesis. This article aims to bring simple and objective information to the scientific community about the work of these three researchers.The Nobel Prize in Chemistry 2016 was granted to Jean-Pierre Sauvage, Sir James F. Stoddart and Bernard (Ben) L. Feringa. These scientists were responsible for the creation and development of molecular machines. The development of such systems represents401113123sem informaçãosem informaçã

O PRÊMIO NOBEL DE QUÍMICA EM 2016: MÁQUINAS MOLECULARES

The Nobel Prize in Chemistry 2016 was granted to Jean-Pierre Sauvage, Sir James F. Stoddart and Bernard (Ben) L. Feringa. These scientists were responsible for the creation and development of molecular machines. The development of such systems represents a breakthrough in the field of supramolecular chemistry, nanotechnology and organic synthesis. This article aims to bring simple and objective information to the scientific community about the work of these three researchers

Modular, Stereocontrolled Cβ–H/Cα–C Activation of Alkyl Carboxylic Acids

The union of two powerful transformations, directed C–H activation and decarboxylative cross-coupling, for the enantioselective synthesis of vicinally functionalized alkyl, carbocyclic, and heterocyclic compounds is described. Starting from simple carboxylic acid building blocks, this modular sequence exploits the residual directing group to access more than 50 scaffolds that would be otherwise extremely difficult to prepare. The tactical use of these two transformations accomplishes a formal vicinal difunctionalization of carbon centers in a way that is modular and thus amenable to rapid diversity incorporation. A simplification of routes to known preclinical drug candidates is presented along with the rapid diversification of an antimalarial compound series. </div

Analysis of Outcomes in Ischemic vs Nonischemic Cardiomyopathy in Patients With Atrial Fibrillation A Report From the GARFIELD-AF Registry

IMPORTANCE Congestive heart failure (CHF) is commonly associated with nonvalvular atrial fibrillation (AF), and their combination may affect treatment strategies and outcomes