Current Organic Chemistry - Volume 22, Issue 5, 2018

Background: Aminopyrimidines represent very important class of functionalized heterocycles having wide applications in organic and medicinal chemistry. Recently, considerable attention has been paid on exploration of aminopyrimidines in pot, atom and step economic multicomponent reactions. Objective: The main objective of this review is to give an overview on the recent applications of aminopyrimidines in multicom Read More

Background: Carbon-based structural materials are widely studied in the field of renewable energy and environmental sciences. Utilization of abundant, natural, renewable energy precursors together with simple and low energy processes can contribute to reduced emissions of greenhouse gas so is considered as fundamental for manufacturing of sustainable nanostructured materials. Description: Among differe Read More

Background: Condensation reactions have attracted increasing attentions due to their important organic transformations in a wide variety of fields of organic chemistry. The main limitations of conventional methods are urgently needed for the development of efficient and heterogeneous catalytic systems. Objective and Method: Supported ionic liquids have broad applications in catalytic reactions due to their significant pr Read More

Phthalocyanine, a large ring complex with 18 π electrons, is derived from the abundant porphyrin in nature. In recent years, the phthalocyanine based materials have aroused great interest of scientists, due to their special skeleton structure, which could be screened and assembled by introducing central ions, axial ligands and substituted groups, and thus obtained materials with special physical and chemical stabilities, Read More

Background: We report a novel MCR4 useful for generating chiral analogs of staurosporine a promiscuous and potent protein kinases inhibitor. Method: Our strategy introduces the use of substituted tetramic acids as chiral precursors which together with an aldehyde, an isocyanide, a dienophile and a Lewis acid lead to hexa-substituted benzenes in one pot. Conclusion: Interestingly, the use of chiral precursors not only Read More