MONDE Kenji

Last updated: Jun 1, 2016 at 14:43
 
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Name
MONDE Kenji
Nickname
handle0167100
E-mail
kmondesci.hokudai.ac.jp
URL
http://www.lfsci.hokudai.ac.jp/labs/infchb/
Affiliation
Hokkaido University
Section
Faculty of Advanced Life Science, Division of Advanced Transdisciplinary Sciences
Job title
Professor
Degree
Doctor of Science(Hokkaido University)
Other affiliation
Frontier Research Center for Post-Genome Science and Technology

Research Areas

 
 

Academic & Professional Experience

 
Apr 2013
 - 
Today
Directer of Post-Genome Research Center, Hokkaido University
 
Apr 2010
 - 
Today
Professor, Hokkaido University
 
Apr 2006
 - 
Mar 2010
Associate Professor, Hokkaido University
 
Jul 2001
 - 
Mar 2006
Associate Professor, Hokkaido University
 
Jul 1996
 - 
Jun 2001
Research Associate, Tohoku University
 
Jan 1995
 - 
Jun 1996
Research Associate, Columbia University
 
Mar 1994
 - 
Jan 1995
Research Associate, Columbia University
 
Apr 1988
 - 
Mar 1994
Research Associate, Hokkaido University
 

Education

 
 
 - 
1986
Graduate School, Division of Natural Science, Hokkaido University
 
 
 - 
1988
Graduate School, Division of Natural Science, Hokkaido University
 
 
 - 
1984
Faculty of Science, Hokkaido University
 

Awards & Honors

 
1992
September, 1992 7th Special Lecture Award for the younger generation (The Chemical Society of Japan)
 

Published Papers

 
What Is the True Structure of D609, a Widely Used Lipid Related Enzyme Inhibitor?
Kato, M., Hammam, M. A. S., Taniguchi, T., Suga, Y., Monde, K.
Org. Lett.   18 768-771   2016   [Refereed]
Stereochemistry of a Rhododaurichromanic Acid Derivative.
Swamy M. M. M., Mandi A., Anetai M., Monde K.
Nat. Prod. Commun.   11 193-195   2016   [Refereed]
Epigenetic stimulation of polyketide production in Chaetomium cancroideum by an NAD+- dependent HDAC inhibitor
Asai, T., Morita, S., Taniguchi, T., Monde, K., Oshima, Y.
Org. Biomol. Chem.   14 646-651   2016   [Refereed]
Highly Efficient Preparation of Sphingoid Bases from Glucosylceramides by Chemoenzymatic Method
Gowda S.B., Usuki S., Hammam M.A.S., Murai Y., Igarashi Y., Monde K.
J. Lipid Res.   57 325-331   2016   [Refereed]
Vibrational CD (VCD) Spectroscopy as a Powerful Tool for Chiral Analysis of Flavor Compounds.
Yaguchi, Y., Nakahashi, A., Miura, N., Taniguchi, T., Sugimoto, D., Emura, M., Zaizen, K., Kusano, Y., .Monde, K.
ACS Symp. Ser.   1212 35-56   2015   [Refereed]
Stereochemical Analysis of Glycerophospholipids by Vibrational Circular Dichroism.
Taniguchi, T., Manai, D., Shibata, M., Itabashi, Y., Monde, K.
J. Am. Chem. Soc.   137 12191-12194   2015   [Refereed]
Genome Mining for Sesterterpenes Using Bifunctional Terpene Synthases Reveals a Unified Intermediate of Di/Sesterterpenes.
Ye, Y., Minami, A., Mandi, A., Liu, C., Taniguchi, T., Kuzuyama, T., Monde, K., Gomi, K., Oikawa H.
J. Am. Chem. Soc.   137 11846-11853   2015   [Refereed]
Asymmetric Nitrocyclopropanation of α-Substituted α,β-Enals Catalyzed by Diphenylprolinol Silyl Ether for the Construction of All-Carbon Quaternary Stereogenic Centers.
Hayashi, Y., Yamazaki, T., Nakanishi, Y., Ono, T., Taniguchi,T., Monde, K., Uchimaru,T.
Eur.J. Org. Chem.   2015 5747-5754   2015   [Refereed]
Revision of the relative and absolute stereochemistry of 3-hydroxydehydroiso-α-lapachone and its derivatives.
Khandelwal, P., Singh, P., Taniguchi, T., Monde, K., Johmoto, K., Uekusa, H., Masubuti, H., Fujimoto, Y.
Phytochemistry Lett.   10 224-229   2014   [Refereed]
Stereoselective synthesis of 1-methoxyspiroindoline phytoalexins and their amino analogues
Salayová, A., Kudličková Z., Baláž M., Budovská M., Pilátová M., Mojžiš J., Monde K., Petrovaj J. Gondová T.
Tetrahedron Asymmetry,   25 1221-1233   2014   [Refereed]

Association Memberships

 
 

Research Grants & Projects

 
Chiral analysis of glycoconjugates by Vibrational Circular Dichroism (VCD)