2016 Member
* TEL & FAX 019-621-(Ext.)
** E-mai (Mail account)@iwate-u.ac.jp
Student |
Name |
Room |
Group*** |
D2 |
Yusuke Taneichi |
313 |
S |
D2 |
Md. Ashraful Alam |
215 |
S |
M2 |
Ryo Sasaki |
314 |
C |
M1 |
Ryo Kowata |
314 |
C |
B4 |
Kaoru Nitatori |
314 |
C |
B4 |
Rei Nishinomiya |
215 |
S |
B4 |
Takuma Kikuchi |
314 |
C |
B4 |
Chiko Kudo |
313 |
S |
B4 |
Yuta Fujiwara |
313 |
S |
B4 |
Chisato Nakamura |
314 |
C |
B4 |
Satsuki Moriya |
314 |
C |
B4 |
Kasumi Shingo |
313 |
S |
*** Groups
S: Organic Synthesis Group directed by Professor Shimada
Researchers in organic synthesis have recently become increasingly interested
in studying reactions specific to heteroatom-containing compounds and applying
them to practical uses. While compounds containing heavier chalcogen elements
are unstable due to their high chemical reactivity, if it were possible
to generate such a compound effectively and manipulate its high chemical
reactivity so that the compound could be used in organic synthesis, it
would enable us to supply useful compounds easily and inexpensively. In
this context, my research focuses on generation of active chemical species,
including the double bond of a chalcogen atom and a carbon atom, and drug
synthesis using them.
C: Catalytic Reaction Group directed by Associate Professor Korenaga
An organometallic catalytic reaction is one of the most utilized methods
for synthesis of various organic compounds. The catalytic activities and
selectivities are controlled by supporting ligands. Among them, a chiral
ligand plays a significant role in asymmetric catalysis to obtain optically
pure compounds such as medicinal drugs. Our group is developing novel ligands
to activate highly the organometallic catalysts. As an alternative, development
of a metal-free organic catalyst is also studied. These catalytic systems
are considered using quantum chemical calculations.
Location
〒020-8551 4-3-5 Ueda, Morioka, Iwate 020-8551, Japan
Department of Chemistry and Bioengineering, Faculty of Engineering, Iwate
University
No. 5 Building, North Wing, 3F