Atsunori
Mori Dr. Eng. b. May 24, 1959 Professor CX-3 Organic Reactions
|
Academic Career |
Nagoya
University, Ph. D.(1987) Nagoya
University, B. S.(1982) |
Professional Career |
Professor, Kobe
Univ.(2005-) Associate Professor,
Chemical Resources Laboratory, Tokyo Inst. Tech. (1995-2005) Research
Associate, JAIST (Japan Advanced Inst. of Sci. &Tech. (1993-1995) Research
Associate, The University of Tokyo (1988-1993) Postdoctral
Fellow, Department of Chem., Univ. of California, Berkeley (1987-1988) |
|
Field of Research |
Organic
Synthesis, Organometallic Chemistry, Materials Science |
|
Research Interest |
Synthetic
methodology of transition metal-catalyzed reactions Synthetic
methodology & materials science of organosilicon compounds Polymer
synthesis with metal-mediated reactions Preparative
methodologies on advanced organic materials |
|
Publications Researcher ID |
・Chirality recognition of
winding vine-shaped heterobiaryls with molecular asymmetry. Kinetic and
dynamic kinetic resolution by Shi's asymmetric epoxidation ・Enantioselective Synthesis of
Macrocyclic Heterobiaryl Derivatives of Molecular Asymmetry by Molybdenum-Catalyzed
Asymmetric Ring-Closing Metathesis ・Ethylaluminum as Ethylene
Source for the Mizoroki-Heck-type Reaction. Rhodium-catalyzed Preparation of
Stilbene Derivatives ・Murahashi Coupling
Polymerization: Nickel(II)–N-Heterocyclic Carbene Complex-Catalyzed
Polycondensation of Organolithium Species of (Hetero)arenes ・Concise Synthesis of
Well-Defined Linear and Branched Oligothiophenes with ・Transition metal-catalyzed
bond-forming reactions at the C‒H bond of heteroaromatic compounds ・Synthesis of Well-defined
Head-to-tail-type Oligothiophenes by Regioselective Deprotonation of
3-Substituted Thio-phenes and Nickel-catalyzed Cross Coupling Reaction ・C‒H Functionalization
polycondensation of chlorothiophenes in the presence of nickel catalyst with
stoichiometric or catalytically-generated magnesium amide J. Am. Chem. Soc. 2011, 133,
9700. ・Palladium-catalyzed C‒H
Functionalization of Heteroarenes with Aryl Bromides and Chlorides ・Stepwise Construction of
Head-to-tail-type Oligothiophenes via Iterative Palladium-catalyzed CH
Arylation and Halogen Exchange ・Direct Amination of Azoles
via Catalytic C−H, N−H Coupling ・Palladium-Catalyzed C-H
Homocoupling of Bromothiophene Derivatives and Synthetic Application to
Well-Defined Oligothiophenes ・Palladium-Catalyzed Coupling
Reactions of Bromothiophenes at the C–H Bond Adjacent to the Sulfur Atom in
the Presence of AgNO3/KF ・One-pot construction of
pyrazoles and isoxazoles with palladium-catalyzed four-component
coupling ・Syntheses and Properties of Donor-Acceptor-Type
2,5-Diarylthiophene and 2,5-diarylthiazole, ・Palladium-catalyzed C-H homocoupling of thiophenes:
Facile construction of bithiophene structure ・Stereodivergent
Syntheses of (Z)- and (E)-Alkenylsilanes via Hydrosilylation of Terminal
Alkynes Catalyzed by Rhodium(I)
Iodide Complexes and Application to Silicon-Containing Polymer
Syntheses ・Carbonylative
Sonogashira Coupling of Terminal Alkynes with Aqueous Ammonia ・Facile synthesis of 2,5-diarylthiazoles via palladium-catalyzed
tandem C-H substitutions. Design of tunable light emission and liquid
crystalline characteristics ・Iridium-catalyzed Mizoroki-Heck-type reaction
of organosilicon compounds ・Sonogashira coupling with aqueous ammonia ・Hydroxorhodium complex-catalyzed carbon-carbon bond-forming
reactions of silanediols with
alfa,beta-unsaturated carbonyl compounds. Mizoroki-Heck type reaction vs
conjugate addition |