Jason Tierney

Bio: Jason Tierney is an academic researcher from Organon International. The author has contributed to research in topics: Organic synthesis & Chemistry. The author has an hindex of 5, co-authored 7 publications receiving 3107 citations.

Microwave Assisted Organic Synthesis

Abstract: Theoretical aspects of microwave dielectric heating, D. Michael P. Mingos.Microwave Accelerated Metal Catalysis. Organic Transformations at Warp Speed, Kristofer Olofsson and Mats Larhed.Heterocyclic chemistry using microwave-assisted approaches, Thierry Besson and Christopher T. Brain.Microwave-assisted Reductions, Timothy N. Danks and Gabriele Wagner.Speed and efficiency in the production of diverse structures: Microwave-assisted multicomponent reactions, Jacob Westman.Integrating Microwave Assisted Synthesis and Solid-Supported Reagents, I.R. Baxendale, A.-L. Lee and S. V. Ley.Microwave-Assisted Solid-Phase Synthesis, Alexander Stadler and C. Oliver Kappe.Time-Savings Associated with Microwave-Assisted Synthesis: A Quantitative Approach, Christopher R. Sarko.Scale-Up of Microwave-assisted Organic Synthesis, Brett A. Roberts and Christopher R. Strauss

1-[(indol-3-yl)carbonyl]piperazine derivatives

Abstract: The present invention relates to 1-[(indol-3-yl)carbonyl]piperazine derivative according to the general formula (I), wherein R represents 1-4 substituents independently selected from H, (C1-4)alkyl (optionally substituted with halogen), (C 1-4)alkyloxy (optionally substituted with halogen), halogen, OH, NH2, CN and NO2; R1 is (C5-8)cycloalkyl or (C5-8)cycloalkenyl; R2 is H, methyl or ethyl; R3, R3', R4' R4', R5, R5' and R6' are independently hydrogen or (C1-4)alkyl, optionally substituted with (C1-4)alkyloxy, halogen or OH; R6 is hydrogen or (C1-4)alkyl, optionally substituted with (C1-4)alkyloxy, halogen or OH; or R6 forms together with R7 a 4-7 membered saturated heterocyclic ring, optionally containing a further heteroatom selected from O and S; R7 forms together with R6 a 4-7 membered saturated heterocyclic ring, optionally containing a further heteroatom selected from O and S; or R7 is H, (C1-4)alkyl or (C3-5)cycloalkyl, the alkyl groups being optionally substituted with OH, halogen or (C1-4)alkyloxy; or a pharmaceutically acceptable salt thereof. The invention also relates to pharmaceutical compositions comprising said 1-[(indol-3-yl)carbonyl]piperazine derivatives, and to the use of these derivatives in the treatment of pain, such as peri-operative pain, chronic pain neuropathic pain, cancer pain, and pain and spasticity associated with multiple sclerosis.

Controlled microwave heating in modern organic synthesis.

Abstract: Although fire is now rarely used in synthetic chemistry, it was not until Robert Bunsen invented the burner in 1855 that the energy from this heat source could be applied to a reaction vessel in a focused manner. The Bunsen burner was later superseded by the isomantle, oil bath, or hot plate as a source for applying heat to a chemical reaction. In the past few years, heating and driving chemical reactions by microwave energy has been an increasingly popular theme in the scientific community. This nonclassical heating technique is slowly moving from a laboratory curiosity to an established technique that is heavily used in both academia and industry. The efficiency of "microwave flash heating" in dramatically reducing reaction times (from days and hours to minutes and seconds) is just one of the many advantages. This Review highlights recent applications of controlled microwave heating in modern organic synthesis, and discusses some of the underlying phenomena and issues involved.

The Sonogashira Reaction: A Booming Methodology in Synthetic Organic Chemistry†

Abstract: 3.7. Palladium Nanoparticles as Catalysts 888 3.8. Other Transition-Metal Complexes 888 3.9. Transition-Metal-Free Reactions 889 4. Applications 889 4.1. Alkynylation of Arenes 889 4.2. Alkynylation of Heterocycles 891 4.3. Synthesis of Enynes and Enediynes 894 4.4. Synthesis of Ynones 896 4.5. Synthesis of Carbocyclic Systems 897 4.6. Synthesis of Heterocyclic Systems 898 4.7. Synthesis of Natural Products 903 4.8. Synthesis of Electronic and Electrooptical Molecules 906

An Overview of the Theory and Applications of Metasurfaces: The Two-Dimensional Equivalents of Metamaterials

Abstract: Metamaterials are typically engineered by arranging a set of small scatterers or apertures in a regular array throughout a region of space, thus obtaining some desirable bulk electromagnetic behavior. The desired property is often one that is not normally found naturally (negative refractive index, near-zero index, etc.). Over the past ten years, metamaterials have moved from being simply a theoretical concept to a field with developed and marketed applications. Three-dimensional metamaterials can be extended by arranging electrically small scatterers or holes into a two-dimensional pattern at a surface or interface. This surface version of a metamaterial has been given the name metasurface (the term metafilm has also been employed for certain structures). For many applications, metasurfaces can be used in place of metamaterials. Metasurfaces have the advantage of taking up less physical space than do full three-dimensional metamaterial structures; consequently, metasurfaces offer the possibility of less-lossy structures. In this overview paper, we discuss the theoretical basis by which metasurfaces should be characterized, and discuss their various applications. We will see how metasurfaces are distinguished from conventional frequency-selective surfaces. Metasurfaces have a wide range of potential applications in electromagnetics (ranging from low microwave to optical frequencies), including: (1) controllable “smart” surfaces, (2) miniaturized cavity resonators, (3) novel wave-guiding structures, (4) angular-independent surfaces, (5) absorbers, (6) biomedical devices, (7) terahertz switches, and (8) fluid-tunable frequency-agile materials, to name only a few. In this review, we will see that the development in recent years of such materials and/or surfaces is bringing us closer to realizing the exciting speculations made over one hundred years ago by the work of Lamb, Schuster, and Pocklington, and later by Mandel'shtam and Veselago.

Cascade reactions in total synthesis.

Abstract: The design and implementation of cascade reactions is a challenging facet of organic chemistry, yet one that can impart striking novelty, elegance, and efficiency to synthetic strategies. The application of cascade reactions to natural products synthesis represents a particularly demanding task, but the results can be both stunning and instructive. This Review highlights selected examples of cascade reactions in total synthesis, with particular emphasis on recent applications therein. The examples discussed herein illustrate the power of these processes in the construction of complex molecules and underscore their future potential in chemical synthesis.

Microwaves in organic synthesis. thermal and non-thermal microwave effects

Abstract: Microwave irradiation has been successfully applied in organic chemistry. Spectacular accelerations, higher yields under milder reaction conditions and higher product purities have all been reported. Indeed, a number of authors have described success in reactions that do not occur by conventional heating and even modifications of selectivity (chemo-, regio- and stereoselectivity). The effect of microwave irradiation in organic synthesis is a combination of thermal effects, arising from the heating rate, superheating or “hot spots” and the selective absorption of radiation by polar substances. Such phenomena are not usually accessible by classical heating and the existence of non-thermal effects of highly polarizing radiation—the “specific microwave effect”—is still a controversial topic. An overview of the thermal effects and the current state of non-thermal microwave effects is presented in this critical review along with a view on how these phenomena can be effectively used in organic synthesis.