Koichi Kodama
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Explore the profile of Koichi Kodama including associated specialties, affiliations and a list of published articles.
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56
Citations
216
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Recent Articles
1.
Kodama K, Obata M, Hirose T
Chempluschem
. 2024 Mar;
89(8):e202400021.
PMID: 38445837
While β-peptides have been paid attention due to their diverse secondary structures, their application to the design of low-molecular-weight gelators (LMWGs) is less explored. In this work, chiral cyclic β-amino...
2.
Hirose T, Kikuchi Y, Nakano T, Ohno T, Kawamura K, Nazri N, et al.
Heliyon
. 2023 Dec;
9(11):e22037.
PMID: 38053870
Liquid crystalline triphenylene derivatives, (n = 6, 12, 14, 16) were prepared using -alkoxycinnamate as the [2+2] photo-cyclization site. (n = 12, 14, 16) showed Col phase and gave crescent-shaped...
3.
Kodama K, Kondo Y, Katayama K, Yanagisawa M, Hirose T
Chirality
. 2023 Nov;
36(2):e23630.
PMID: 37957824
Chiral N-substituted secondary 1,2-aminoalcohols have been developed for the enantioseparation of ortho-halomandelic acids (o-X-MAs) via diastereomeric salt formation. Two structural isomers, N-methyl-2-amino-1,2-diphenylethanol and N-benzyl-2-amino-2-phenylethanol, showed high separation abilities for o-X-MAs...
4.
Muralidhar J, Salikolimi K, Adachi K, Hashizume D, Kodama K, Hirose T, et al.
J Am Chem Soc
. 2023 Jul;
145(31):16973-16977.
PMID: 37427843
Toward renewable energy for global leveling, compounds that can store ammonia (NH), a carbon-free energy carrier of hydrogen, will be of great value. Here, we report an organic-inorganic halide perovskite...
5.
Chandrasekaran S, Tambo M, Yamazaki Y, Muramatsu T, Kanda Y, Hirose T, et al.
Molecules
. 2023 Jan;
28(1).
PMID: 36615310
Enantioseparation of 3-hydroxycarboxylic acids via diastereomeric salt formation was demonstrated using 2-amino-1,2-diphenylethanol (ADPE) and cinchonidine as the resolving agents. Racemic 3-hydroxy-4-phenylbutanoic acid (-), 3-hydroxy-4-(4-chlorophenyl)butanoic acid (-), and 3-hydroxy-5-phenylpentanoic acid (-)...
6.
Kodama K, Obata M, Sugimura S, Yuhara H, Hirose T
Chemistry
. 2022 Dec;
29(11):e202202692.
PMID: 36461621
This study reports the formation of low-molecular-weight gelators based on carboxylic acids derived from chiral cyclicβ-amino acids. The effect of their stereochemistry on the gelation of organic solvents was investigated,...
7.
Kanai H, Yamada K, Salikolimi K, Kodama K, Ishida Y
Chemistry
. 2022 Sep;
28(62):e202201940.
PMID: 36073840
The photocyclodimerization of 2-anthracenecarboxylic acid has been extensively studied as a model reaction of asymmetric photochemistry. So far, numerous chiral environments have been employed to control this photoreaction, while the...
8.
Kodama K, Takase F, Hirose T
RSC Adv
. 2022 Apr;
11(30):18162-18170.
PMID: 35480945
Amidine-based optically active resolving agents for enantiomer separation of axially chiral 1,1'-biaryl-2,2'-diols have been developed. A strongly basic amidine bearing no substituents on its nitrogen atoms enables the formation of...
9.
Muralidhar J, Kodama K, Hirose T, Ito Y, Kawamoto M
Nanomaterials (Basel)
. 2022 Jan;
12(1).
PMID: 35010002
Single-walled carbon nanotubes (SWCNTs) have received extensive research attention owing to their extraordinary optical, electrical, and mechanical properties, which make them particularly attractive for application in optoelectronic devices. However, SWCNTs...
10.
Kanai H, Yamada K, Kodama K, Ishida Y
Chirality
. 2021 Nov;
34(2):295-305.
PMID: 34792805
Chiral amphiphiles are useful for controlling the structures and properties of supramolecular assemblies, but their stereocontrolled synthesis is generally difficult, because their long alkyl chains tend to bring unfavorable effects...