SHIMOKAWA Jun

J-GLOBAL         Last updated: Nov 7, 2019 at 11:26
 
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Name
SHIMOKAWA Jun
E-mail
shimokawakuchem.kyoto-u.ac.jp
Affiliation
Kyoto University
Twitter ID
jshimok
ORCID ID
0000-0002-4023-4640

Research Interests

 
 

Research Areas

 
 

Academic & Professional Experience

 
Jan 2018
 - 
Today
Associate Professor, Graduare School of Science, Kyoto University 
 
Apr 2012
 - 
Dec 2017
Assistant Professor, Graduate School of Pharmaceutical Sciences, Nagoya University
 

Education

 
Apr 2003
 - 
Mar 2006
Graduate School of Pharmaceutical Sciences, The University of Tokyo
 
Apr 1998
 - 
Mar 2003
Faculty of Pharmaceutical Sciences, The University of Tokyo
 

Awards & Honors

 
Apr 2018
The Young Scientists’ Prize, The Commendation for Science and Technology by the Minister of Education, Culture, Sports, Science and Technology, Ministry of Education, Culture, Sports, Science and Technology
 
Oct 2017
Synthetic Studies on Heteropolycyclic Natural Products: Strategy via the Development of Novel Reactions and Divergent Approaches, Chemist Award BCA 2017, MSD Life Science Foundation
 
Mar 2017
The Pharmaceutical Society of Japan Award for Young Scientists, The Pharmaceutical Society of Japan
 
Nov 2016
Asian Core Program/Advanced Research Network Lectureship Award, Malaysia, Asian Core Program
 
Nov 2016
Asian Core Program/Advanced Research Network Lectureship Award, China, Asian Core Program
 

Published Papers

 
Hiroki Yamagishi, Jun Shimokawa, Hideki Yorimitsu
Synlett   30(13) 1551-1554   Aug 2019   [Refereed]
Atsushi Kaga, Tomohiro Fukushima, Jun Shimokawa, Masato Kitamura
Synthesis   51(17) 3214-3220   May 2019   [Refereed]
Jun Shimokawa, Kazuo Nagasawa
Heterocycles   99(1) 521-533   Dec 2018   [Refereed]
Hiroki Yamagishi, Shun Tsuchiya, Hayate Saito, Keisuke Nogi, Jun Shimokawa, Hideki Yorimitsu
Heterocycles   99(1) 301-309   Oct 2018   [Refereed]
Shimokawa Jun
JOURNAL OF SYNTHETIC ORGANIC CHEMISTRY JAPAN   76(5) 458-461   May 2018   [Refereed]
Shimokawa Jun
CHEMICAL & PHARMACEUTICAL BULLETIN   66(2) 105-115   Feb 2018   [Refereed]
Kazuya Douki, Jun Shimokawa, Masato Kitamura
Organic & Biomolecular Chemistry   17 1727-1730   Oct 2018   [Refereed]
Shimokawa Jun, Fukuyama Tohru
JOURNAL OF SYNTHETIC ORGANIC CHEMISTRY JAPAN   75(11) 1115-1124   Nov 2017   [Refereed]
Abe Kazuhiro, Shimokawa Jun, Naito Mao, Munson Keith, Vagin Olga, Sachs George, Suzuki Hiroshi, Tani Kazutoshi, Fujiyoshi Yoshinori
SCIENTIFIC REPORTS   7    Jul 2017   [Refereed]
Kazuya Douki, Hiroyuki Ono, Tohru Taniguchi, Jun Shimokawa, Masato Kitamura, Tohru Fukuyama
Journal of the American Chemical Society   138(44) 14578-14581   Oct 2016   [Refereed]
Jun Shimokawa, Koji Chiyoda, Hirotatsu Umihara, Tohru Fukuyama
Chemical and Pharmaceutical Bulletin   64(8) 1239-1241   May 2016   [Refereed]
Hirotatsu Unihara, Tomomi Yoshino, Jun Shimokawa, Masato Kitamura, Tohru Fukuyama
Angewandte Chemie, International Edition   55(24) 6915-6918   May 2016   [Refereed]
Ideue E, Shimokawa J, Fukuyama T
Organic Letters   17(20) 4964-4967   Oct 2015   [Refereed]
Jun Shimokawa
Tetrahedron Letters   55 6156-6162   Nov 2014   [Refereed]
© 2014 The Author. Published by Elsevier Ltd. Divergent strategy in natural product synthesis allows the comprehensive synthesis of family natural products. Efficient formulation of this idea requires the biosynthetic/biosynthesis-inspired insight...
Takayuki Yamakawa, Eiji Ideue, Jun Shimokawa, Tohru Fukuyama
Angewandte Chemie International Edition   53 8808   Aug 2014   [Refereed]
Ren Takeuchi, Jun Shimokawa, Tohru Fukuyama
Chemical Science   5 2003-2006   May 2014   [Refereed]
The epidithiodioxopiperazine skeleton is found in a variety of biologically active compounds. Despite numerous attempts at constructing this highly functionalized structure within a bicyclo[2.2.2]octane skeleton, asymmetric synthesis of this uniqu...
Kaise H, Shimokawa J, Fukuyama T
Organic letters   16(3) 727-729   Feb 2014   [Refereed]
Katsushi Kitahara, Jun Shimokawa, Tohru Fukuyama
Chemical Science   5 904-907   Jan 2014   [Refereed]
The asymmetric synthesis of spirotryprostatin A was achieved by employing an intramolecular Heck reaction to introduce the quaternary spiro center. The stereochemistry of the reaction was controlled by a tethering system, which was selectively int...
Yuri Iwai, Takashi Ozaki, Ryo Takita, Masanobu Uchiyama, Jun Shimokawa, Tohru Fukuyama
Chemical Science   4 1111-1119   Mar 2013   [Refereed]
The traditional McFadyen-Stevens reaction requires harsh alkaline reaction conditions, thus precluding application to the synthesis of aliphatic aldehydes. Our modified McFadyen-Stevens reaction enables the transformation from the N,N-acylsulfonyl...

Research Grants & Projects

 
Ministry of Education, Culture, Sports, Science and Technology: Grants-in-Aid for Scientific Research(特別推進研究)
Project Year: 2008 - 2012    Investigator(s): Tohru FUKUYAMA
(抄録なし)
Ministry of Education, Culture, Sports, Science and Technology: Grants-in-Aid for Scientific Research(若手研究(B))
Project Year: 2009 - 2010    Investigator(s): Jun SHIMOKAWA
Establishment of the reliable conditions for the radical-mediated indole construction has made it possible to achieve the highly efficient synthesis of tryprostatins A and B. Lowering the reaction temperature by means of V-70, a radical initiator,...
Ministry of Education, Culture, Sports, Science and Technology: Grants-in-Aid for Scientific Research(基盤研究(S))
Project Year: 2003 - 2007    Investigator(s): Tohru FUKUYAMA
The main focus of our research in this term of the grant-in-aid (S) is the synthesis of natural products bearing highly complicated structures. We have already developed the aryl-amination reaction using copper catalyst, and this strategy was appl...