Synthetic Organic Chemistry
Staffs
Seiichi Nakamura, Ph.D., Professor
Eisaku Ohashi, Ph.D., Research Associate
Eisaku Ohashi, Ph.D., Research Associate
Research Project
- Studies on the Synthesis of Biologically Active Natural Products
- Development of Efficient Methods for Construction of Molecular Architectures
- Development of Highly Selective Synthetic Reactions
Natural products have played a significant role in the development of organic chemistry, especially in the area of fine organic synthesis. Compounds with unprecedented molecular architecture and multiple functional groups have created opportunities for devising new strategies and methodologies as well as evaluating the synthetic utility of known methods and reactions. In addition, making target molecules in a practical fashion represents one of the major challenges in synthetic organic chemistry.
Our research has focused on the synthesis of biologically active natural products, and the development of new reactions and strategies for organic synthesis.
(1) We have accomplished the total synthesis of the calcium channel activator pinnatoxin A (left) by exploiting a tandem double hemiketal formation/hetero-Michael addition sequence to construct its [6,5,6]-dispiroketal ring system. Our first total synthesis of polygalolide A (right) by a carbonyl ylide cycloaddition strategy serves to provide stereochemical insight into the biosynthesis of this class of natural products.
Our research has focused on the synthesis of biologically active natural products, and the development of new reactions and strategies for organic synthesis.
(1) We have accomplished the total synthesis of the calcium channel activator pinnatoxin A (left) by exploiting a tandem double hemiketal formation/hetero-Michael addition sequence to construct its [6,5,6]-dispiroketal ring system. Our first total synthesis of polygalolide A (right) by a carbonyl ylide cycloaddition strategy serves to provide stereochemical insight into the biosynthesis of this class of natural products.
