Tags: Organic Seminar

It might be an understatement in saying the interest in Metal Organic Frameworks (MOFs) and their vast array of topologies, constitutions and applications have incurred great interest over the past two decades. Many areas of chemical research have been impacted in the potential that MOFs bring to the table. These include gas storage and separations, chemical catalysis, endeavors in the removal of harmful and toxic environmental chemicals,…
Daphniphyllum alkaloids have a rich history dating back to the isolation of Daphniphyllum macropodum Miquel in 1909 by Yagi.1 Pioneering work in the 1960s by Hirata and colleagues resulted in the isolation of daphniphylline and yuzurimine alkaloids, and subsequently, a total of over 330 Daphniphyllum alkaloids have been reported from the Daphniphyllum genus.2-5 In view of their intriguing biological activities including anti-cancer and  …
Over the past few decades, photoredox catalysis has emerged as a powerful tool for new bond formation. Acting as an oxidant or a reductant, an excited-state metal complex can generate reactive radical intermediates via a single-electron transfer process. The most commonly used transition-metal photocatalysts are ruthenium or iridium complexes. Our group has utilized chromium(III) complexes in a variety of different photoredox transformations.…
Lignin is the world’s second most abundant biopolymer and the world’s largest source of biobased aromatics (1). Occurring as an adhesive which binds together the cellulose fibers in the cell walls of woody plants, lignin has been largely cast aside as a waste byproduct of pulping procedures. Since the main industrial pulping procedures focus on the production of paper, the fate of lignin usually involves combustion to produce heat (2). This…
Electrolysis in synthetic organic chemistry has a rich history dating back to the 19th century. Many advances have been done with the use of electrolysis in the past, e.g. Kolbe’s decarboxylative dimerization, 1 Tafel’s electrolytic rearrangement, 2 Simmons’s C-H fluorination.3 Since then the popularity of the electrolysis in synthetic organic chemistry has drastically decreased. In the past decade transition metal-catalyzed C-H…
Despite the ever-increasing availability and applicability of computational methods to questions of chemical significance, many chemists from purely experimental backgrounds find it difficult to begin integrating these methods into their research. To reduce this barrier of entry and catalyze non-computational chemists’ ability to take advantage of the insights computational studies can provide, we have developed a suite of tools, collectively…
Glycosylation of certain proteins by oxygen-linked mannose (O-mannose) is known as O-mannosylation, and this process is essential for growth and development in animals.1-4 Defective O-mannosylation of α-dystroglycan, the most well studied O-mannosylated mammalian protein, leads to congenital muscular dystrophies and neurological defects.4-6 Mannose is linked to proteins through the serine or threonine side chain oxygen. Glycosyl transferase…
Phorbol, a Tigliane natural product first isolated in 1934 by Dr.Flaschenträger and Dr. Wolffersdorff, drove 17 research groups to develop the synthesis of it for over 30 years and report over 40 synthesis papers because of their potent biological activities to promote the tumor by activation of the protein kinase C and the anticancer activity.  The structure of the phorbol, first determined by Dr. Heck in 1967, was a congested tetracyclic…
Bond formation via metal-catalyzed selective C–H functionalization is well appreciated and often relies on the directing capability of the substrate. That is, the appropriate positioning of a Lewis basic functional group can present the metal catalyst center at a specific site, enabling activation of otherwise unreactive C–H bonds. The Lewis basicity of alcohols can be exploited to impart directing capabilities allowing for the capacity to…
The first part of my talk centers on the application of cation clock reactions for the determination of relative reaction kinetics in sialidation reactions. The formation of glycosidic bonds is perhaps the most important bond forming reaction in glycoscience, playing a critical role in the assembly of all glycoconjugates. In general, the control of the glycosylation reaction is a key ingredient to engineering better stereoselective…