Norito Takenaka
Assistant Professor, Organic Chemistry

B.A./M.A., Boston University, 1996
Ph.D., The University of Chicago, 2002

E-mail: n.takenaka@miami.edu

Research Interests:

The Takenaka group is interested in synthetic organic chemistry in broad terms, which range from asymmetric catalysis to synthesis of complex natural products. New methods offer new ways to assemble the complex molecular architecture and execution of resulting new synthetic strategies, in turn, lead to new insights and discoveries in method development. Methodology and synthesis are expected to complement to each other. The group’s focus is on the design and development of conceptually new catalysts for the promotion of selective chemical transformations of broad synthetic utility. Of particular interest is the development of environmentally benign, highly versatile Lewis/Brønsted acids that catalyze carbon-carbon bond formation with the highest level of selectivity and efficiency, which is of central importance in organic synthesis. The second major focus of our program is on the synthesis of structurally interesting and biologically significant natural products that not only encompass our own synthetic methods but also inspire further methodology and strategy development, including mechanistic aspects. The objectives of such endeavors are the discovery and development of new synthetic technology that provides efficient access to potential pharmaceuticals in green, non-toxic fashion, as well as better understanding of organic chemistry.

External Funding

American Cancer Society
Florida Department of Public Health

Full List of Publications

Selected Publications

“2-Aminopyridinium Ions Activate Nitroalkenes through Hydrogen Bonding” Takenaka, N.; Sarangthem, R. S.; Seerla, S. K. Org. Lett. 2007, 9, 2819-2822.

“Asymmetric Conjugate Addition of Silyl Enol Ethers Catalyzed by Tethered Bis(8-quinolinolato) Aluminum Complexes” Takenaka, N.; Abell, J. P.; Yamamoto, Y. J. Am. Chem. Soc. 2007, 129, 742-743.

“Axially Chiral Biaryl Diols (BAMOLs) Catalyze Highly Enantioselective Hetero Diels-Alder Reactions Through Hydrogen Bonding” Unni, A. K.; Takenaka, N.; Yamamoto, H.; Rawal, V. H. J. Am. Chem. Soc.2005, 127, 1336-1337.

“Catalytic, Highly Enantio- and Diastereoselective Pinacol Coupling Reaction with a New Tethered Bis(8-quinolinolato) Ligand” Takenaka, N.; Xia, G.; Yamamoto, H. J. Am. Chem. Soc.2004, 126, 13198-13199.

“The First Catalytic Enantioselective Diels-Alder Reactions of 1,2-Dihydropyridine: Efficient Syntheses of Optically Active 2-Azabicyclo[2.2.2]octanes with Chiral BINAM Derived Cr (III) Salen Complexes.”Takenaka, N.; Huang, Y.; Rawal, V. H. Tetrahedron, 2002, 58, 8299-8305.

“Asymmetric Crotylation Reactions in the Synthesis of Polypropionate Derived Macrolide: Application to the Total Synthesis of Oleandolide” Hu, T.; Takenaka, N.; Panek, J. S. J. Am. Chem. Soc.2002, 124, 12806-12815.

“Total Synthesis of Oleandolide” Hu, T.; Takenaka, N.; Panek, J. S. J. Am. Chem. Soc.1999, 121, 9229-9230.

“Double-Stereodifferentiating Crotylation Reactions with Chiral (E)-Crotylsilanes. Evaluation of a New Approach for the Synthesis of Polypropionate-Derived Natural Products” Jain, N. F.; Takenaka, N.; Panek, J. S. J. Am. Chem. Soc.1996, 118, 12475-12476.

 

 


 
Department of Chemistry
1301 Memorial Drive
Coral Gables, Florida 33146-0431
(305) 284-2174
Leave Feedback
Privacy Information
Copyright © 2004