Tokushima University / Educator and Researcher Directory --- Karanjit, Sangita

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https://researchmap.jp/karanjit0227 (researchmap)

Field of Study

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Book / Paper

Academic Paper (Judged Full Paper):

1.	Kimika Kayano, Tomohiro Tsutsumi, Yoshiko Murata, Chie Ogasa, Takehiro Watanabe, Ryota Sato, Sangita Karanjit and Kosuke Namba : Epoxide ring-opening reactions for abundant production of mugineic acids and nicotianamine probes., Angewandte Chemie International Edition, Vol.63, No.20, e202401411, 2024. (Summary) A succinct synthetic approach to mugineic acids and 2'-hydroxynicotianamine was established. Unlike all other synthetic methods, this approach utilized epoxide ring-opening reactions to form two C-N bonds and is characterized by the absence of redox reactions. Mugineic acid was synthesized from three readily available fragments on a gram scale in 6 steps. The protected 2'-hydroxynicotianamine was also synthesized in 4 steps, and the dansyl group, serving as a fluorophore, was introduced through a click reaction after propargylation of the 2'-hydroxy group. The dansyl-labeled nicotianamine (NA) iron complexes were internalized by oocytes overexpressing ZmYS1 (from maize) or PAT1 (from human) transporters, indicating successful transport of the synthesized NA-probe through these transporters. (Keyword) Epoxy Compounds / Humans / Molecular Structure / Azetidinecarboxylic Acid (Tokushima University Institutional Repository) ● Metadata: 119292 (Link to Publication Site) ● Publication site (DOI): 10.1002/anie.202401411 (Link to Search Site for Scientific Articles) ● PubMed @ National Institutes of Health, US National Library of Medicine (PMID): 38500479 ● Search Scopus @ Elsevier (PMID): 38500479 ● Search Scopus @ Elsevier (DOI): 10.1002/anie.202401411 (Tokushima University Institutional Repository: 119292, DOI: 10.1002/anie.202401411, PubMed: 38500479)
2.	Yuna Kondo, Tenta Nakamura, Daisuke Tsuji, Ryota Sato, Sangita Karanjit, Reiko Akagi and Kosuke Namba : Development of 1,3a,6a-triazapentalene derivatives as practical erasable fluorescent cell staining reagents., Tetrahedron Letters, Vol.138, 154986, 2024. (Link to Publication Site) ● Publication site (DOI): 10.1016/j.tetlet.2024.154986 (Link to Search Site for Scientific Articles) ● Search Scopus @ Elsevier (DOI): 10.1016/j.tetlet.2024.154986 (DOI: 10.1016/j.tetlet.2024.154986)
3.	Ryuichi Sumida, Misa Okuda, Akane Mera, Masaki Inoue, Sangita Karanjit, Kanji Niwa, Tomohiro Tsutsumi, Ryota Sato, Atsushi Nakayama, Naonobu Tanaka, Masataka Oda and Kosuke Namba : A suitable stereoisomer of vibrioferrin probes for iron uptake of Vibrio parahaemolyticus, Chemistry Letters, 2023. (Tokushima University Institutional Repository) ● Metadata: 118228 (Link to Publication Site) ● Publication site (DOI): 10.1246/cl.230166 (Link to Search Site for Scientific Articles) ● CiNii @ National Institute of Informatics (CRID): 1360016863185963264 ● Search Scopus @ Elsevier (DOI): 10.1246/cl.230166 (Tokushima University Institutional Repository: 118228, DOI: 10.1246/cl.230166, CiNii: 1360016863185963264)
4.	Yuhei Nogi, Noriko Saito-Tarashima, Sangita Karanjit and Noriaki Minakawa : Synthesis and Behavior of DNA Oligomers Containing the Ambiguous Z-Nucleobase 5-Aminoimidazole-4-carboxamide, Molecules, Vol.28, No.7, 3265, 2023. (Summary) 5-Amino-1-β-D-ribofuranosylimidazole-4-carboxamide 5'-monophosphate (ZMP) is a central intermediate in de novo purine nucleotide biosynthesis. Its nucleobase moiety, 5-aminoimidazole-4-carboxamide (Z-base), is considered an ambiguous base that can pair with any canonical base owing to the rotatable nature of its 5-carboxamide group. This idea of ambiguous base pairing due to free rotation of the carboxamide has been applied to designing mutagenic antiviral nucleosides, such as ribavirin and T-705. However, the ambiguous base-pairing ability of Z-base has not been elucidated, because the synthesis of Z-base-containing oligomers is problematic. Herein, we propose a practical method for the synthesis of Z-base-containing DNA oligomers based on the ring-opening reaction of an -dinitrophenylhypoxanthine (Hxa) base. Thermal denaturation studies of the resulting oligomers revealed that the Z-base behaves physiologically as an A-like nucleobase, preferentially forming pairs with T. We tested the behavior of Z-base-containing DNA oligomers in enzyme-catalyzed reactions: in single nucleotide insertion, Klenow fragment DNA polymerase recognized Z-base as an A-like analog and incorporated dTTP as a complementary nucleotide to Z-base in the DNA template; in PCR amplification, Taq DNA polymerase similarly incorporated dTTP as a complementary nucleotide to Z-base. Our findings will contribute to the development of new mutagenic antiviral nucleoside analogs. (Keyword) Aminoimidazole Carboxamide / DNA / Base Pairing / Nucleosides / Nucleotides (Link to Publication Site) ● Publication site (DOI): 10.3390/molecules28073265 (Link to Search Site for Scientific Articles) ● PubMed @ National Institutes of Health, US National Library of Medicine (PMID): 37050028 ● Search Scopus @ Elsevier (PMID): 37050028 ● Search Scopus @ Elsevier (DOI): 10.3390/molecules28073265 (DOI: 10.3390/molecules28073265, PubMed: 37050028)
5.	Daisuke Tsuji, Atsushi Nakayama, RIko Yamamoto, Shuji Nagano, Takashi Taniguchi, Ryota Sato, Sangita Karanjit, Naoki Muguruma, Tetsuji Takayama, Kohji Itoh and Kosuke Namba : 1,3a,6a-Triazapentalene derivatives as photo-induced cytotoxic small fluorescent dyes, Communications Chemistry, Vol.6, No.1, 37, 2023. (Summary) 1,3a,6a-Triazapentalene (TAP) is a compact fluorescent chromophore whose fluorescence properties vary greatly depending on the substituents on the TAP ring. This study investigated the photo-induced cytotoxicities of various TAP derivatives. Among the derivatives, 2-p-nitrophenyl-TAP showed significant cytotoxicity to HeLa cells under UV irradiation but no cytotoxicity without UV. In addition, the photo-induced cytotoxicity of 2-p-nitirophenyl-TAP was found to be cancer cell selective and effective against HeLa cells and HCT 116 cells. Under UV irradiation, 2-p-nitrophenyl-TAP generated reactive oxygen species (ROS) that induced an apoptosis and ferroptosis in cancer cells. Therefore, it was revealed that 2-p-nitrophenyl-TAP is the most compact dye that can generate ROS by photoirradiation. (Tokushima University Institutional Repository) ● Metadata: 118227 (Link to Publication Site) ● Publication site (DOI): 10.1038/s42004-023-00838-0 (Link to Search Site for Scientific Articles) ● PubMed @ National Institutes of Health, US National Library of Medicine (PMID): 36813913 ● Search Scopus @ Elsevier (PMID): 36813913 ● Search Scopus @ Elsevier (DOI): 10.1038/s42004-023-00838-0 (Tokushima University Institutional Repository: 118227, DOI: 10.1038/s42004-023-00838-0, PubMed: 36813913)
6.	Yuki Kimura, Eisaku Ohashi, Sangita Karanjit, Takashi Taniguchi, Atsushi Nakayama, Hiroshi Imagawa, Ryota Sato and Kosuke Namba : Total synthesis of proposed structures of 4,10-dihydroxy 8,12-guaianolides, Organic Letters, Vol.24, No.17, 3297-3301, 2022. (Summary) The first total syntheses of two 4,10-dihydroxy-8,12-guaianolides that were reported to be natural products were achieved. Toward the syntheses of a collection of related guaianolides, the typical 5,7-fused system of 8,12-guaianolides was constructed by a ring expansion reaction of a hydroxylated coronafacic acid analogue that can be practically synthesized and optically resolved. The total syntheses of these compounds revealed that the previously reported structures of both natural products were incorrect. (Keyword) Biological Products / Molecular Structure (Tokushima University Institutional Repository) ● Metadata: 117329 (Link to Publication Site) ● Publication site (DOI): 10.1021/acs.orglett.2c01215 (Link to Search Site for Scientific Articles) ● PubMed @ National Institutes of Health, US National Library of Medicine (PMID): 35446586 ● Search Scopus @ Elsevier (PMID): 35446586 ● Search Scopus @ Elsevier (DOI): 10.1021/acs.orglett.2c01215 (Tokushima University Institutional Repository: 117329, DOI: 10.1021/acs.orglett.2c01215, PubMed: 35446586)
7.	Sangita Karanjit, Emiko Tanaka, L. K. Shrestha, Atsushi Nakayama, Katsuhiko Ariga and Kosuke Namba : A heterogeneous bifunctional silica-supported Ag₂O/Im⁺Cl^- catalyst for efficient CO₂ conversion, Catalysis Science & Technology, Vol.12, 3297-3301, 2022. (Link to Publication Site) ● Publication site (DOI): 10.1039/D2CY00194B (Link to Search Site for Scientific Articles) ● Search Scopus @ Elsevier (DOI): 10.1039/D2CY00194B (DOI: 10.1039/D2CY00194B)
8.	Eisaku Ohashi, Sangita Karanjit, Atsushi Nakayama, Kohei Takeuchi, Sherif E Emam, Hidenori ANDO, Tatsuhiro Ishida and Kosuke Namba : Efficient construction of the hexacyclic ring core of palau'amine: the pK_a concept for proceeding with unfavorable equilibrium reactions, Chemical Science, Vol.12, 2021. (Tokushima University Institutional Repository) ● Metadata: 116279 (Link to Publication Site) ● Publication site (DOI): 10.1039/D1SC03260G (Link to Search Site for Scientific Articles) ● Search Scopus @ Elsevier (DOI): 10.1039/D1SC03260G (Tokushima University Institutional Repository: 116279, DOI: 10.1039/D1SC03260G)
9.	Atsushi Nakayama, Tenta Nakamura, Tabassum Ara, tatsuya fukuta, Sangita Karanjit, Takeshi Harada, Asuka Oda, Hideo Sato, Masahiro Abe, Kentaro Kogure and Kosuke Namba : Development of a novel antioxidant based on a dimeric dihydroisocoumarin derivative, Tetrahedron Letters, Vol.74, 153176, 2021. (Tokushima University Institutional Repository) ● Metadata: 116179 (Link to Publication Site) ● Publication site (DOI): 10.1016/j.tetlet.2021.153176 (Link to Search Site for Scientific Articles) ● Summary page in Scopus @ Elsevier: 2-s2.0-85107022552 (Tokushima University Institutional Repository: 116179, DOI: 10.1016/j.tetlet.2021.153176, Elsevier: Scopus)
10.	Sangita Karanjit, Ayumu Tamura, Masaya Kashihara, Kazuki Ushiyama, L. K. Shreshta, Katsuhiko Ariga and Kosuke Namba : Hydrotalcite-Supported Ag/Pd Bimetallic Nanoclusters Catalyzed Oxidation and One-Pot Aldol Reaction in Water, Catalysts, Vol.10, No.10, 1120, 2020. (Tokushima University Institutional Repository) ● Metadata: 116176 (Link to Publication Site) ● Publication site (DOI): 10.3390/catal10101120 (Link to Search Site for Scientific Articles) ● Search Scopus @ Elsevier (DOI): 10.3390/catal10101120 (Tokushima University Institutional Repository: 116176, DOI: 10.3390/catal10101120)
11.	Atsushi Nakayama, Tenta Nakamura, Toshihiro Zaima, Saho Fujimoto, Sangita Karanjit and Kosuke Namba : Concise Total Synthesis of Tronocarpine, Angewandte Chemie International Edition, Vol.60, No.2, 635-639, 2020. (Summary) A concise total synthesis of tronocarpine, a chippiine-type indole alkaloid, was accomplished. The key feature of this total synthesis is a one-pot construction of the pentacyclic skeleton containing an azabicyclo[3.3.1]nonane core by tandem cyclization from an indole derivative with all carbon side chains and functional groups. This tandem cyclization consists of α,β-unsaturated aldehyde formation, intramolecular aldol reaction, six-membered lactamization, azide reduction, and seven-membered lactamization. The stereochemical outcome in this tandem cyclization is controlled by the stereocenter at the C14 position. This strategy can be utilized to synthesize other chippiine-type alkaloids with azabicyclo[3.3.1]nonane skeletons. (Tokushima University Institutional Repository) ● Metadata: 116180 (Link to Publication Site) ● Publication site (DOI): 10.1002/anie.202009966 (Link to Search Site for Scientific Articles) ● PubMed @ National Institutes of Health, US National Library of Medicine (PMID): 32969565 ● Search Scopus @ Elsevier (PMID): 32969565 ● Search Scopus @ Elsevier (DOI): 10.1002/anie.202009966 (Tokushima University Institutional Repository: 116180, DOI: 10.1002/anie.202009966, PubMed: 32969565)
12.	Tsutsumi Tomohiro, Saitoh Arisa, Kasai Tomoyo, Chu MengYue, Sangita Karanjit, Atsushi Nakayama and Kosuke Namba : Synthesis and evaluation of 1,1,7,7-tetramethyl-9-azajulolidine (TMAJ) as a highly active derivative of N,N-dimethylaminopyridine, Tetrahedron Letters, Vol.61, No.26, 152047, 2020. (Tokushima University Institutional Repository) ● Metadata: 115070 (Link to Publication Site) ● Publication site (DOI): 10.1016/j.tetlet.2020.152047 (Link to Search Site for Scientific Articles) ● Search Scopus @ Elsevier (DOI): 10.1016/j.tetlet.2020.152047 (Tokushima University Institutional Repository: 115070, DOI: 10.1016/j.tetlet.2020.152047)
13.	Atsushi Nakayama, Hideo Satoh, Tenta Nakamura, Hamada Mai, Nagano Shuji, Shuhei Kameyama, Furue Yui, Hayashi Naoki, Kamoshida Go, Sangita Karanjit, Oda Masataka and Kosuke Namba : Synthesis and Antimicrobial Evaluation of Side-Chain Derivatives based on Eurotiumide A, Marine Drugs, Vol.18, No.2, 92, 2020. (Tokushima University Institutional Repository) ● Metadata: 115585 (Link to Publication Site) ● Publication site (DOI): 10.3390/md18020092 (Link to Search Site for Scientific Articles) ● Search Scopus @ Elsevier (DOI): 10.3390/md18020092 (Tokushima University Institutional Repository: 115585, DOI: 10.3390/md18020092)
14.	Atsushi Nakayama, Hideo Satoh, Shuji Nagano, Sangita Karanjit, Hiroshi Imagawa and Kosuke Namba : Asymmetric Total Syntheses and Structure Elucidations of (+)-Eurotiumide F and (+)-Eurotiumide G, Chemical & Pharmaceutical Bulletin, Vol.67, No.9, 953-958, 2019. (Summary) Asymmetric total syntheses of dihydropyran containing natural products, (+)-eurotiumide F and (+)-eurotiumide G have been described. These total syntheses revealed the absolute configuration of eurotiumide F and G, and confirmed the reported structure of eurotiumide F and revised the reported structure of eurotiumide G. Highlight of these syntheses is thermal rearrangement with 4-methoxyisochroman-1-one derivative having propargyl ether on phenolic ether under thermal condition to construct dihydropyran ring. X-Ray crystallographic analysis of (+)-eurotiumide G clarified the stereochemistry at the C1-position. (Tokushima University Institutional Repository) ● Metadata: 113683 (Link to Publication Site) ● Publication site (DOI): 10.1248/cpb.c18-00948 (Link to Search Site for Scientific Articles) ● PubMed @ National Institutes of Health, US National Library of Medicine (PMID): 31474735 ● Summary page in Scopus @ Elsevier: 2-s2.0-85071659929 (Tokushima University Institutional Repository: 113683, DOI: 10.1248/cpb.c18-00948, PubMed: 31474735, Elsevier: Scopus)
15.	Tomohiro Tsutsumi, Sangita Karanjit, Atsushi Nakayama and Kosuke Namba : A Concise Asymmetric Total Synthesis of (+)-Epilupinine, Organic Letters, Vol.21, No.8, 2620-2624, 2019. (Summary) Asymmetric total synthesis of (+)-epilupinine was achieved in just three steps using only commercially available common reagents. The total synthesis involved alkylations of N-nosylamide, ozone oxidation, and sequential reactions of the removal of the nosyl group, intramolecular dehydrative condensation, intramolecular Mannich reaction catalyzed by l-proline, and a reduction. (Tokushima University Institutional Repository) ● Metadata: 113631 (Link to Publication Site) ● Publication site (DOI): 10.1021/acs.orglett.9b00607 (Link to Search Site for Scientific Articles) ● PubMed @ National Institutes of Health, US National Library of Medicine (PMID): 30963767 ● Summary page in Scopus @ Elsevier: 2-s2.0-85064687055 (Tokushima University Institutional Repository: 113631, DOI: 10.1021/acs.orglett.9b00607, PubMed: 30963767, Elsevier: Scopus)
16.	Ryota Sato, Ryuji Okamoto, Takumi Ishizuka, Atsushi Nakayama, Sangita Karanjit and Kosuke Namba : Microwave-assisted Tertiary Carbon Radical Reaction for Construction of Quaternary Carbon Center, Chemistry Letters, Vol.48, No.5, 414-417, 2019. (Tokushima University Institutional Repository) ● Metadata: 113632 (Link to Publication Site) ● Publication site (DOI): 10.1246/cl.190040 (Link to Search Site for Scientific Articles) ● Summary page in Scopus @ Elsevier: 2-s2.0-85066142615 (Tokushima University Institutional Repository: 113632, DOI: 10.1246/cl.190040, Elsevier: Scopus)
17.	Ito Masami, Mera Akane, Mashimo Toshiki, Seki Tomohiro, Sangita Karanjit, Ohashi Eisaku, Atsushi Nakayama, Kitamura Kei, Hamura Toshiyuki, Ito Hajime and Kosuke Namba : Synthesis and Evaluation of 1,3a,6a-triazapentalene (TAP)-bonded system, Chemistry - A European Journal, Vol.24, No.67, 17727-17733, 2018. (Summary) A method of synthesizing a directly connected 1,3a,6a-triazapentalene (TAP) ring system as a linearly bonded aromatic system with a planar form was established. Various TAP-dimers and a 2-alkyl-TAP-trimer were synthesized and their fluorescence properties were evaluated. Although the direct connection of the TAP ring with other TAP rings did not affect the fluorescence properties in diluted solvent, TAP-dimers showed unique fluorescence properties derived from the aggregation state under highly concentrated conditions. In particular, TAP-dimer 5 f showed aggregation-induced emission in highly concentrated solution, and 5 b showed typical mechanochromic fluorescence in the solid state despite their compact molecular size. (Tokushima University Institutional Repository) ● Metadata: 113633 (Link to Publication Site) ● Publication site (DOI): 10.1002/chem.201804733 (Link to Search Site for Scientific Articles) ● PubMed @ National Institutes of Health, US National Library of Medicine (PMID): 30298702 ● Summary page in Scopus @ Elsevier: 2-s2.0-85057344150 (Tokushima University Institutional Repository: 113633, DOI: 10.1002/chem.201804733, PubMed: 30298702, Elsevier: Scopus)
18.	Tsubasa Okamoto, Miki Shibata, Sangita Karanjit, Atsushi Nakayama, Masahiro Yoshida and Kosuke Namba : Direct Synthesis of Polycyclic Tropinones by a Condensation-[4+3]-Cycloaddition Cascade Reaction., Chemistry - A European Journal, Vol.24, No.38, 9508-9513, 2018. (Summary) A concise method of constructing polycyclic tropinone frameworks was developed. The single-step synthesis of polycyclic tropinone consists of an intramolecular [4+3] cycloaddition reaction of N-nosyl-pyrrole with oxyallyl cation that was generated in situ by an intermolecular condensation reaction of the nucleophilic functional groups on a tethered pyrrole with the aldehyde of 2-(silyloxy)-acrolein. This cascade reaction afforded various polycyclic tropinones including tri-, tetra-, and pentacyclic systems in high yields as single diastereomers. (Tokushima University Institutional Repository) ● Metadata: 113634 (Link to Publication Site) ● Publication site (DOI): 10.1002/chem.201802011 (Link to Search Site for Scientific Articles) ● PubMed @ National Institutes of Health, US National Library of Medicine (PMID): 29701268 ● Summary page in Scopus @ Elsevier: 2-s2.0-85049583439 (Tokushima University Institutional Repository: 113634, DOI: 10.1002/chem.201802011, PubMed: 29701268, Elsevier: Scopus)
19.	Atsushi Nakayama, Hideo Sato, Sangita Karanjit, Naoki Hayashi, Masataka Oda and Kosuke Namba : Asymmetric Total Synthesis and Structure Revisions of Eurotiumide A and Eurotiumide B, and Evaluation of their Fluorescent Properties as Natural Probes., European Journal of Organic Chemistry, Vol.2018, No.29, 4013-4017, 2018. (Tokushima University Institutional Repository) ● Metadata: 113684 (Link to Publication Site) ● Publication site (DOI): 10.1002/ejoc.201800535 (Link to Search Site for Scientific Articles) ● Search Scopus @ Elsevier (DOI): 10.1002/ejoc.201800535 (Tokushima University Institutional Repository: 113684, DOI: 10.1002/ejoc.201800535)
20.	Sangita Karanjit, Masaya Kashihara, Atsushi Nakayama, Lok Kumar Shrestha, Katsuhiko Ariga and Kosuke Namba : Highly active and reusable hydrotalcite-supported Pd(0) catalyst for Suzuki coupling reactions of aryl bromides and chlorides, Tetrahedron, Vol.74, No.9, 948-954, 2018. (Link to Publication Site) ● Publication site (DOI): 10.1016/j.tet.2017.12.056 (Link to Search Site for Scientific Articles) ● Summary page in Scopus @ Elsevier: 2-s2.0-85040597957 (DOI: 10.1016/j.tet.2017.12.056, Elsevier: Scopus)

Proceeding of International Conference:

1.	Ohashi Eisaku, Takeuchi Kohei, Atsushi Nakayama, Tanino Keiji, Sangita Karanjit and Kosuke Namba : Studies on the Second Generation Synthesis of Palau'amine, The 9th Junior International Conference on Cutting-Edge Organic Chemistry Asia, Sep. 2019.
2.	Tsutsumi Tomohiro, Sangita Karanjit, Atsushi Nakayama and Kosuke Namba : A Concise Asymmetric Total Synthesis of (+)-epilupinine, 27th International Society of Heterocyclic Chemistry Congress, Sep. 2019.
3.	Ohashi Eisaku, Takeuchi Kohei, Atsushi Nakayama, Sangita Karanjit, Tanino Keiji and Kosuke Namba : Studies on the Second Generation Synthesis of Palau'amine, 27th International Society of Heterocyclic Chemisty Congress, Sep. 2019.
4.	Sangita Karanjit, Masaya Kashihara, Atsushi Nakayama and Kosuke Namba : Pd0-Hydrotalcite: A Versatile Heterogeneous Catalyst for Bond Transformation under Mild Condition, The 11th International Symposium on Integrated Synthesis, Awaji, Nov. 2017.

Proceeding of Domestic Conference:

1.	KONDOH Yuna, NAKAMURA Tenta, Riko Yamamoto, Ryota Sato, Sangita Karanjit, Daisuke Tsuji, 赤木玲子 and Kosuke Namba : 長波長領域で活性化する1,3a,6a-トリアザペンタレン(TAP)類の合成と光応答型細胞毒性の評価, 日本薬学会第144年会, Mar. 2024.
2.	Ryuichi Sumida, INOUE Masaki, Ryota Kotaka, Ryota Sato, Atsushi Nakayama, Sangita Karanjit and Kosuke Namba : Calyciphylline F の全合成, 日本薬学会第144年会, Mar. 2024.
3.	YUKI Kimura, Eisaku Ohhashi, Sangita Karanjit, Ryota Sato and Kosuke Namba : Palau'amineの第3世代合成研究, 日本薬学会第144年会, Mar. 2024.
4.	HAGIMOTO Daichi, Ryota Sato, Sangita Karanjit and Kosuke Namba : Alstonisine の全合成研究, 日本薬学会第144年会, Mar. 2024.
5.	Takashi Taniguchi, YUKI Kimura, Ryota Sato, Sangita Karanjit and Kosuke Namba : Guianolide型セスキテルペンラクトン類の第二世代合成研究, 日本薬学会第144年会, Mar. 2024.
6.	MAJIMA Rei, KOHDAI Kawata, Ryota Sato, Sangita Karanjit and Kosuke Namba : Scabronine Gの全合成研究, 日本薬学会第144年会, Mar. 2024.
7.	Jun Hashimura, Shuji Nagano, Ryota Sato, Sangita Karanjit and Kosuke Namba : Eleganine Aの合成研究, 日本薬学会第144年会, Mar. 2024.
8.	Sangita Karanjit, Tanaka Emiko, MAJIMA Rei, Ryota Sato and Kosuke Namba : Catalytic carboxylation and decarboxylation approach for the construction of bicyclic intermediates as core structural motifs in natural products, 日本化学会第104回春季年会, Mar. 2024.
9.	KONDOH Yuna, NAKAMURA Tenta, Riko Yamamoto, Ryota Sato, Sangita Karanjit, Daisuke Tsuji, 赤木玲子 and Kosuke Namba : 長波長領域で活性化する1,3a,6a-トリアザペンタレン(TAP)類の合成と光応答型細胞毒性の評価, 日本プロセス化学会東四国地区フォーラムセミナー, Jan. 2024.
10.	Ryuichi Sumida, INOUE Masaki, Ryota Kotaka, Ryota Sato, Atsushi Nakayama, Sangita Karanjit and Kosuke Namba : Calyciphylline F の全合成研究, 第34回日本プロセス化学会東四国地区フォーラムセミナー, Jan. 2024.
11.	Takashi Taniguchi, YUKI Kimura, Ryota Sato, Sangita Karanjit and Kosuke Namba : Guianolide型セスキテルペンラクトン類の第二世代合成研究, 第62回日本薬学会・日本薬剤師会・日本病院薬剤師会中国四国支部学術大会, Oct. 2023.
12.	KONDOH Yuna, NAKAMURA Tenta, Riko Yamamoto, Sangita Karanjit, Ryota Sato, Daisuke Tsuji and Kosuke Namba : 赤色光応答型1,3a,6a-トリアザペンタレン(TAP)類の開発と光細胞毒性の評価, 第62回日本薬学会・日本薬剤師会・日本病院薬剤師会中国四国支部学術大会, Oct. 2023.
13.	YUKI Kimura, Eisaku Ohhashi, Sangita Karanjit, Ryota Sato and Kosuke Namba : Palau'amineの第3世代合成研究, 第62回日本薬学会・日本薬剤師会・日本病院薬剤師会中国四国支部学術大会, Oct. 2023.
14.	Jun Hashimura, Shuji Nagano, Ryota Sato, Sangita Karanjit and Kosuke Namba : Eleganine Aの合成研究, 第62回日本薬学会・日本薬剤師会・日本病院薬剤師会中国四国支部学術大会, Oct. 2023.
15.	Riko Yamamoto, Shuji Nagano, Akane Mera, Sangita Karanjit, Atsushi Nakayama, Daisuke Tsuji, 赤木玲子, Kouji Itou and Kosuke Namba : 1,3a,6a-トリアザペンタレン類の合成と光応答型細胞毒性の評価, 第62回日本薬学会・日本薬剤師会・日本病院薬剤師会中国四国支部学術大会, Oct. 2023.
16.	MAJIMA Rei, KOHDAI Kawata, Ryota Sato, Sangita Karanjit and Kosuke Namba : Scabronine Gの全合成研究, 第62回日本薬学会・日本薬剤師会・日本病院薬剤師会中国四国支部学術大会, Oct. 2023.
17.	BIWATANI Saki, YUKI Kimura, KIMIKA Kayano, Sangita Karanjit, 藤原和樹 and Kosuke Namba : 植物の鉄取り込み機構に基づいたCG病治療薬の開発研究, 第62回日本薬学会・日本薬剤師会・日本病院薬剤師会中国四国支部学術大会, Oct. 2023.
18.	KOHDAI Kawata, Ryuji Okamoto, Kohki Katoh, Sangita Karanjit, Ryota Sato and Kosuke Namba : Nagelamide Q の全合成研究, 第62回日本薬学会・日本薬剤師会・日本病院薬剤師会中国四国支部学術大会, Oct. 2023.
19.	Ryuichi Sumida, INOUE Masaki, Ryota Kotaka, Ryota Sato, Atsushi Nakayama, Sangita Karanjit and Kosuke Namba : Calyciphylline F の全合成研究, 第62回日本薬学会・日本薬剤師会・日本病院薬剤師会中国四国支部学術大会, Oct. 2023.
20.	KOHDAI Kawata, 岡本龍治, Kohki Katoh, Sangita Karanjit, Ryota Sato and Kosuke Namba : Nagelamide Q の全合成研究, 第65回天然物有機化合物討論会, Sep. 2023.
21.	Takashi Taniguchi, YUKI Kimura, Ryota Sato, Sangita Karanjit and Kosuke Namba : Guianolide型セスキテルペンラクトン類の第二世代合成研究, 第37回若手化学者のための化学道場, Sep. 2023.
22.	Ryuichi Sumida, INOUE Masaki, Ryota Kotaka, Ryota Sato, Atsushi Nakayama, Sangita Karanjit and Kosuke Namba : Calyciphylline F の全合成研究, 第37回若手化学者のための化学道場, Sep. 2023.
23.	Jun Hashimura, Shuji Nagano, Ryota Sato, Sangita Karanjit and Kosuke Namba : Eleganine Aの合成研究, 第37回若手化学者のための化学道場, Sep. 2023.
24.	YUKI Kimura, Eisaku Ohhashi, Sangita Karanjit, Ryota Sato and Kosuke Namba : Palau'amineの第3世代合成研究, 日本薬学会第143年会, Mar. 2023.
25.	Riko Yamamoto, Shuji Nagano, Akane Mera, Sangita Karanjit, Atsushi Nakayama, Daisuke Tsuji, 赤木玲子, Kouji Itou and Kosuke Namba : 1,3a,6a-トリアザペンタレン類の合成と光応答型細胞毒性の評価, 日本薬学会第143年会, Mar. 2023.
26.	Kimika Kayano, Tomohiro Tsutsumi, Sangita Karanjit, Ryota Sato and Kosuke Namba : ムギネ酸類の効率的全合成, 日本薬学会第143年会, Mar. 2023.
27.	Ten Katoh, Tenta Nakamura, Sangita Karanjit, Ryota Sato and Kosuke Namba : アブシジン酸の全合成と蛍光プローブへの展開, 日本薬学会第143年会, Mar. 2023.
28.	Riko Yamamoto, Shuji Nagano, Akane Mera, Sangita Karanjit, Atsushi Nakayama, Daisuke Tsuji, Kouji Itou and Kosuke Namba : 1,3a,6a-トリアザペンタレン類の合成と光応答型細胞毒性の評価, 第61回日本薬学会・日本薬剤師会・日本病院薬剤師会中四国支部学術大会, Nov. 2022.
29.	Yuki Kimura, Eisaku Ohhashi, Sangita Karanjit, Ryota Sato and Kosuke Namba : Palau'amineの第3世代合成研究, 第61回日本薬学会・日本薬剤師会・日本病院薬剤師会中四国支部学術大会, Nov. 2022.
30.	Emiko Tanaka, Sangita Karanjit and Kosuke Namba : 二機能性を有する不均一系シリカ担持イミダゾリウム塩/酸化銀触媒を用いた効率的な二酸化炭素挿入環化反応., 第61回日本薬学会・日本薬剤師会・日本病院薬剤師会中国四国支部学術大会, Nov. 2022.
31.	Ryuichi Sumida, Masaki Inoue, Misa Okuda, Akane Mera, Sangita Karanjit, Atsushi Nakayama and Kosuke Namba : Vibrioferrin蛍光標識プローブの合成と評価, 第61回日本薬学会・日本薬剤師会・日本病院薬剤師会中国四国支部学術大会, Nov. 2022.
32.	Kimika Kayano, Tomohiro Tsutsumi, 小笠千恵, 村田佳子, Sangita Karanjit, Ryota Sato and Kosuke Namba : 哺乳類の鉄輸送機構解明に向けたニコチアナミンプローブの効率的合成, 第61回日本薬学会・日本薬剤師会・日本病院薬剤師会中国四国支部学術大会, Nov. 2022.
33.	Takashi Taniguchi, Yuki Kimura, Ryota Sato, Sangita Karanjit and Kosuke Namba : Guaianolide型セスキテルペンラクトン類の第二世代合成, 第61回日本薬学会・日本薬剤師会・日本病院薬剤師会中国四国支部学術大会, Nov. 2022.
34.	Ten Katoh, Tenta Nakamura, Sangita Karanjit, Ryota Sato and Kosuke Namba : アブシジン酸の全合成と蛍光プローブへの展開, 第61回日本薬学会・日本薬剤師会・日本病院薬剤師会中国四国支部学術大会, Nov. 2022.
35.	Jun Hashimura, Shuji Nagano, Sangita Karanjit, Ryota Sato and Kosuke Namba : Eleganine Aの全合成研究, 第61回日本薬学会・日本薬剤師会・日本病院薬剤師会中国四国支部学術大会, Nov. 2022.
36.	Kimika Kayano, Tomohiro Tsutsumi, 小笠千恵, 村田佳子, Sangita Karanjit, Ryota Sato and Kosuke Namba : 哺乳類の鉄輸送機構解明に向けたニコチアナミンプローブの効率的合成, 第36回若手化学者のための化学道場, Sep. 2022.
37.	Emiko Tanaka, Sangita Karanjit and Kosuke Namba : 二機能性を有する不均一系シリカ担持イミダゾリウム塩/酸化銀触媒を用いた効率的な二酸化炭素挿入環化反応., 第36回若手化学者のための化学道場, Sep. 2022.
38.	Yuki Kimura, Eisaku Ohhashi, Sangita Karanjit, Takashi Taniguchi, Atsushi Nakayama, 今川洋, Ryota Sato and Kosuke Namba : Guaianolide型セスキテルペンラクトン類の全合成, 第64回天然有機化合物討論会, Sep. 2022.
39.	Emiko Tanaka, Sangita Karanjit and Kosuke Namba : 二機能性を有する不均一系シリカ担持イミダゾリウム塩/酸化銀触媒を用いた効率的な二酸化炭素挿入環化反応, 創薬懇話会2022, Jun. 2022.
40.	Yuki Kimura, Eisaku Ohashi, Sangita Karanjit, Atsushi Nakayama and Kosuke Namba : Guaianolide型セスキテルペンラクトン類の全合成研究, 日本薬学会第142年会, Mar. 2022.
41.	Emiko Tanaka, Sangita Karanjit and Kosuke Namba : 二機能を有する不均一系シリカ担持イミダゾリウム塩/酸化銀触媒を用いた効率的な二酸化炭素挿入環化反応, 日本薬学会第142年会, Mar. 2022.
42.	Kimika Kayano, Tomohiro Tsutsumi, 小笠千恵, 村田佳子, Sangita Karanjit and Kosuke Namba : 植物体内の鉄輸送機構解明に向けたニコチアナミンプローブの開発研究, 日本薬学会第142年会, Mar. 2022.
43.	Emiko Tanaka, Sangita Karanjit and Kosuke Namba : 二機能を有する不均一系シリカ担持イミダゾリウム塩/酸化銀触媒を用いた効率的な二酸化炭素挿入環化反応, 第60回日本薬学会・日本薬剤師会・日本病院薬剤師会中国四国支部学術大会, Nov. 2021.
44.	Kimika Kayano, tomohiro Tsutsumi, Sangita Karanjit and Kosuke Namba : 植物体内の鉄輸送機構解明に向けたニコチアナミンプローブの開発研究, 第60回日本薬学会・日本薬剤師会・日本病院薬剤師会中国四国支部学術大会, Nov. 2021.
45.	Masaki Inoue, Ryota Sato, Ryota Kotaka, Atsushi Nakayama, Sangita Karanjit, 谷野圭持 and Kosuke Namba : Calyciphylline Fの全合成研究, 第60回日本薬学会・日本薬剤師会・日本病院薬剤師会中国四国支部学術大会, Nov. 2021.
46.	Saki Funabiki, Sayaka Sasaki, Haruka Mukaiyama, Daisuke Tsuji, Yoshiko Murata, Takenori Yamamoto, Sangita Karanjit, Atsushi Nakayama, Kouji Itou and Kosuke Namba : イネ科植物の鉄取り込み機構解明を志向したトランスポーター標識プローブの開発, 第60回日本薬学会・日本薬剤師会・日本病院薬剤師会中国四国支部学術大会, Nov. 2021.
47.	Yuki Kimura, Eisaku Ohashi, Sangita Karanjit, Atsushi Nakayama and Kosuke Namba : Guaianolide型セスキテルペンラクトン類の全合成研究, 第60回日本薬学会・日本薬剤師会・日本病院薬剤師会中国四国支部学術大会, Nov. 2021.
48.	Tenta Nakamura, Toshihiro Zaima, Sangita Karanjit, Atsushi Nakayama and Kosuke Namba : Tronocarpineの短工程全合成, 第50回複素環化学討論会, Oct. 2021.
49.	Yuki Kimura, Eisaku Ohashi, Sangita Karanjit, Atsushi Nakayama and Kosuke Namba : Guaianolide型セスキテルペンラクトン類の全合成研究, 第37回有機合成セミナー, Sep. 2021.
50.	Saki Funabiki, Sayaka Sasaki, Haruka Mukaiyama, Daisuke Tsuji, Yoshiko Murata, Takenori Yamamoto, Sangita Karanjit, Atsushi Nakayama, Kouji Itou and Kosuke Namba : イネ科植物の鉄取り込み機構解明を志向したトランスポーター標識プローブの開発, 創薬懇話会2021, Jun. 2021.
51.	Masaki Inoue, Ryota Sato, Ryota Kotaka, Ryuichi Fuchigami, Atsushi Nakayama, Sangita Karanjit and Kosuke Namba : Calyciphylline Fの全合成研究, 創薬懇話会2021, Jun. 2021.
52.	Yuki Kimura, Eisaku Ohashi, Sangita Karanjit, Atsushi Nakayama and Kosuke Namba : Guaianolide型セスキテルペンラクトン類の全合成研究, 創薬懇話会2021, Jun. 2021.
53.	Tenta Nakamura, Toshihiro Zaima, Sangita Karanjit, Atsushi Nakayama and Kosuke Namba : Chippiine型アルカロイドTronocarpineの短工程全合成, 創薬懇話会2021, Jun. 2021.
54.	井上雅貴, 佐藤亮太, 古高涼太, Atsushi Nakayama, Sangita Karanjit and Kosuke Namba : CalyciphyllineFの全合成研究, 日本薬学会第141年会(広島), Mar. 2021.
55.	井上雅貴, 佐藤亮太, 古高涼太, Atsushi Nakayama, Sangita Karanjit and Kosuke Namba : CalyciphyllineFの全合成研究, 第59回日本薬学会・日本薬剤師会・日本病院薬剤師会中国四国支部学術大会, Dec. 2020.
56.	Misa Okuda, Akane Mera, 小田真隆, Sangita Karanjit, Atsushi Nakayama and Kosuke Namba : 蛍光性シデロフォアを利用した微生物検出法の開発, 第59回日本薬学会・日本薬剤師会・日本病院薬剤師会中国四国支部学術大会, Dec. 2020.
57.	初梦玥, Tomohiro Tsutsumi, Tomoyo Kasai, Sangita Karanjit, Atsushi Nakayama and Kosuke Namba : 高触媒活性DMAP誘導体の合成研究, 第59回日本薬学会・日本薬剤師会・日本病院薬剤師会中国四国支部学術大会, Dec. 2020.
58.	Eisaku Ohhashi, Kohei Takeuchi, Sangita Karanjit, Atsushi Nakayama, 谷野圭持 and Kosuke Namba : Palau'amineの第二世代合成研究, 第62回天然物有機化合物討論会, Sep. 2020.
59.	Shuji Nagano, Tsubasa Okamoto, Miki Shibata, Sangita Karanjit, Atsushi Nakayama and Kosuke Namba : Stemofolineの合成研究-五環性コア骨格構築のモデル研究, 日本薬学会第140年会, Mar. 2020.
60.	船曵早希, 佐々木彩花, 向山はるか, Daisuke Tsuji, 村田佳子, Takenori Yamamoto, Sangita Karanjit, Atsushi Nakayama, Kouji Itou and Kosuke Namba : イネ科植物の鉄イオン取り込みトランスポーター標識プローブの合成と評価, 日本薬学会第140年会, Mar. 2020.
61.	斎藤亜梨紗, 堤大洋, 笠井知世, Sangita Karanjit, Atsushi Nakayama and Kosuke Namba : 高触媒活性DMAP誘導体の合成研究, 日本薬学会第140年会, Mar. 2020.
62.	奥田実沙, 米良茜, 小田真隆, Sangita Karanjit, Atsushi Nakayama and Kosuke Namba : 蛍光性シデロフォアを利用した微生物検出法の開発, 日本薬学会第140年会, Mar. 2020.
63.	Eisaku Ohhashi, Kohei Takeuchi, Sangita Karanjit, Atsushi Nakayama, 谷野圭持 and Kosuke Namba : Palau'amineの第二世代合成研究, 日本薬学会第140年年会, Mar. 2020.
64.	Tomohiro Tsutsumi, Sangita Karanjit, Atsushi Nakayama and Kosuke Namba : (+)-epilupinine3, 日本薬学会第140年会, Mar. 2020.
65.	斎藤亜梨紗, 堤大洋, 笠井知世, Sangita Karanjit, Atsushi Nakayama and Kosuke Namba : 高触媒活性DMAP誘導体の合成研究, 2019年度第3回(第31回)日本プロセス化学会東四国フォーラムセミナー, Jan. 2020.
66.	船曵早希, 佐々木彩花, Daisuke Tsuji, 村田佳子, Sangita Karanjit, Atsushi Nakayama, Kouji Itou, Takenori Yamamoto and Kosuke Namba : イネ科植物の鉄イオン取り込み機構解明に向けた標識プローブの合成と評価, 第58回日本薬学会・日本薬剤師会・日本病院薬剤師会中国四国支部学術大会, Nov. 2019.
67.	斎藤亜梨紗, 堤大洋, 笠井知世, Sangita Karanjit, Atsushi Nakayama and Kosuke Namba : 高触媒活性DMAP誘導体の合成研究, 第58回日本薬学会・日本薬剤師会・日本病院薬剤師会中国四国支部学術大会, Nov. 2019.
68.	長野秀嗣, 岡本翼, 柴田弥希, Sangita Karanjit, Atsushi Nakayama and Kosuke Namba : Stemofolineの合成研究-五環性コア骨格構築のモデル研究, 第58回日本薬学会・日本薬剤師会・日本病院薬剤師会中国四国支部学術大会, Nov. 2019.
69.	堤大洋, Sangita Karanjit, Atsushi Nakayama and Kosuke Namba : (+)-epilupinine3, 第58回日本薬学会・日本薬剤師会・日本病院薬剤師会中国四国支部学術大会, Nov. 2019.
70.	奥田実沙, 米良茜, 小田真隆, Sangita Karanjit, Atsushi Nakayama and Kosuke Namba : 蛍光性シデロフォアを利用した微生物検出法の開発, 2019年度第2回(第30回)日本プロセス化学会東四国フォーラムセミナー, Oct. 2019.
71.	大橋栄作, 竹内公平, Sangita Karanjit, Atsushi Nakayama, Kosuke Namba and 谷野圭持 : Palau'amineの第二世代合成研究, 2019年度第2回(第30回)日本プロセス化学会東四国フォーラムセミナー, Oct. 2019.
72.	奥田実沙, 米良茜, 小田真隆, Sangita Karanjit, Atsushi Nakayama and Kosuke Namba : 蛍光性シデロフォアを利用した微生物検出法の開発, 第35回有機合成化学協会中四国支部若手化学者のための化学道場in島根, Sep. 2019.
73.	占部敦美, 津川稜, 西尾賢, 佐々木彩花, 鈴木基史, 村田佳子, 増田寛志, Sangita Karanjit, 小林高範, Atsushi Nakayama and Kosuke Namba : アルカリ性不良土壌の緑地化を目指したムギネ酸類の実用化研究, 第14回トランスポーター研究会年会, Jul. 2019.
74.	船曵早希, 佐々木彩花, 向山はるか, 村田佳子, Sangita Karanjit, Atsushi Nakayama, Kosuke Namba, 占部敦美, Daisuke Tsuji and Kouji Itou : イネ科植物の鉄イオン取り込み機構の解明に向けた化学プローブの開発, 第14回トランスポーター研究会年会, Jul. 2019.
75.	長野秀嗣, 岡本翼, 柴田弥希, Sangita Karanjit, Atsushi Nakayama and Kosuke Namba : 多環式トロピノンの一挙構築を用いるStemofolineの合成研究, 第54回天然物化学談話会, Jul. 2019.
76.	堤大洋, Sangita Karanjit, Atsushi Nakayama and Kosuke Namba : (+)-epilupinine3, 第54回天然物化学談話会, Jul. 2019.
77.	大橋栄作, 竹内公平, Sangita Karanjit, Atsushi Nakayama, Kosuke Namba and 谷野圭持 : Palau'amineの第二世代合成研究, 天然物化学談話会, Jul. 2019.
78.	柏原雅也, Sangita Karanjit, Atsushi Nakayama and Kosuke Namba : 高活性かつ再利用可能なHydrotalcite担持Pd触媒の開発とその応用, 第52回有機金属若手の会夏の学校, Jun. 2019.
79.	浜田麻衣, Sangita Karanjit, Atsushi Nakayama and Kosuke Namba : Resorcylic Acid Lactone類の網羅的合成, 第52回有機金属若手の会夏の学校, Jun. 2019.
80.	堤大洋, Sangita Karanjit, Atsushi Nakayama and Kosuke Namba : (+)-epilupinine3, 創薬懇話会2019 in 秋保, Jun. 2019.
81.	船曵早希, 佐々木彩花, 向山はるか, 村田佳子, Daisuke Tsuji, Sangita Karanjit, Atsushi Nakayama and Kosuke Namba : イネ科植物の鉄イオン取り込み機構の解明に向けた化学プローブの開発, 2019年度第1回(第29回)日本プロセス化学会東四国フォーラムセミナー, Jun. 2019.
82.	堤大洋, Sangita Karanjit, Atsushi Nakayama and Kosuke Namba : (+)-epilupinine3, 2019年度第1回(第29回)日本プロセス化学会東四国フォーラムセミナー, Jun. 2019.
83.	Atsumi Urabe, Ryo Tsugawa, Satoshi Nishio, Sayaka Sasaki, 鈴木基史, 増田寛志, Sangita Karanjit, Atsushi Nakayama, 小林高範 and Kosuke Namba : ムギネ酸類の実用化研究, 日本薬学会第139年会, Mar. 2019.
84.	Eisaku Ohhashi, Kohei Takeuchi, Atsushi Nakayama, 谷野圭持, Kosuke Namba and Sangita Karanjit : Palau'amineの第二世代合成研究, 日本薬学会第139年会, Mar. 2019.
85.	Mai Hamada, Shinichiroh Nakayama, Atsushi Nakayama, Sangita Karanjit and Kosuke Namba : Resorcylic Acid Lactone類の網羅的合成, 2018年第3回(第28回)プロセス化学東四国フォーラムセミナー, Jan. 2019.
86.	Mai Hamada, Shinichiroh Nakayama, Atsushi Nakayama, Sangita Karanjit and Kosuke Namba : Resorcylic Acid Lactone類，LL-Z1640-2を基盤とした新規生物活性分子の提案，合成研究, 第57回日本薬学会・日本薬剤師会・日本病院薬剤師会中国四国支部学術大会, Nov. 2018.
87.	Misa Okuda, Tomohiro Tsutsumi, Atsushi Nakayama, Sangita Karanjit and Kosuke Namba : シリカ固定化ホスフィン配位子を用いたPd及びPd/Au合金ナノクラスター触媒の開発, 第57回日本薬学会・日本薬剤師会・日本病院薬剤師会中国四国支部学術大会, Nov. 2018.
88.	Tsubasa Okamoto, Sangita Karanjit, Atsushi Nakayama, Kosuke Namba and 柴田弥希 : 複雑なトロパン骨格の効率的構築法の開発とStemofolineの全合成への展開, 第57回日本薬学会・日本薬剤師会・日本病院薬剤師会中国四国支部学術大会, Nov. 2018.
89.	Sayaka Sasaki, Haruka Mukaiyama, Daisuke Tsuji, 村田佳子, Sangita Karanjit, Atsushi Nakayama, Kouji Itou and Kosuke Namba : 鉄取り込み機構解明を志向したトランスポーター標識プローブの開発, 第57回日本薬学会・日本薬剤師会・日本病院薬剤師会中国四国支部学術大会, Nov. 2018.
90.	Masaya Kashihara, Sangita Karanjit, Atsushi Nakayama and Kosuke Namba : 不均一Pd触媒担持材料としての新規ビピリジンポリマーの開発とそのPd触媒的酸化反応への応用, 第57回日本薬学会・日本薬剤師会・日本病院薬剤師会中国四国支部学術大会, Nov. 2018.
91.	Saho Fujimoto, Atsushi Nakayama, Toshihiro Zaima, Sangita Karanjit and Kosuke Namba : Tronocarpineの全合成, 第57回日本薬学会・日本薬剤師会・日本病院薬剤師会中国四国支部学術大会, Nov. 2018.
92.	Hideo Satoh, Atsushi Nakayama, Sangita Karanjit, 林直樹, 小田正隆 and Kosuke Namba : Eurotiumide類の網羅的不斉全合成, 2018年度第2回(第27回)プロセス化学東四国フォーラムセミナー, Oct. 2018.
93.	Atsushi Nakayama, Toshihiro Zaima, Saho Fujimoto, Sangita Karanjit and Kosuke Namba : Chippiine 型アルカロイド類の全合成研究., 第 60 回天然有機化合物討論会, Sep. 2018.
94.	Atsumi Urabe, Ryo Tsugawa, Satoshi Nishio, Sayaka Sasaki, 鈴木基史, 増田寛志, Sangita Karanjit, Atsushi Nakayama, 小林高範, Kosuke Namba and Aung Sann May : アルカリ性不良土壌での農耕を指向したムギネ酸類の実用化研究, 第34回若手化学者のための化学道場, Sep. 2018.
95.	Atsumi Urabe, Ryo Tsugawa, Satoshi Nishio, Sayaka Sasaki, 鈴木基史, 増田寛志, Sangita Karanjit, Atsushi Nakayama, 小林高範, Kosuke Namba and Aung Sann May : アルカリ性不良土壌での農耕を指向したムギネ酸類の実用化研究, 創薬懇話会2018 in 志賀島, Jun. 2018.
96.	Masaya Kashihara, Sangita Karanjit, Atsushi Nakayama and Kosuke Namba : 高活性かつ再利用可能なHydrotalcite担持Pd触媒の開発とその応用, 創薬懇話会2018 in 志賀島, Jun. 2018.
97.	Mai Hamada, Shinichiroh Nakayama, Atsushi Nakayama, Sangita Karanjit and Kosuke Namba : Resorcylic Acid Lactone類の網羅的合成, 2018年第1回(第26回)プロセス化学東四国フォーラムセミナー, Jun. 2018.
98.	Atsushi Nakayama, Toshihiro Zaima, Saho Fujimoto, Sangita Karanjit and Kosuke Namba : Chippiine型アルカロイド類の全合成研究, 第16回次世代を担う有機化学シンポジウム, May 2018.
99.	Atsushi Nakayama, Toshihiro Zaima, Sangita Karanjit and Kosuke Namba : Dippinine Bの全合成研究, 第56回日本薬学会第138年会, Mar. 2018.
100.	Masaya Kashihara, Sangita Karanjit, Atsushi Nakayama and Kosuke Namba : Highly active and stable heterogeneous Pd-Hydrotalcite for Suzuki coupling reaction of artless halides, 第56回日本薬学会第138年会, Mar. 2018.
101.	Mai Hamada, Shinichiroh Nakayama, Atsushi Nakayama, Sangita Karanjit and Kosuke Namba : LL-Z1640-2を含むResorcylic Acid Lactone類の網羅的合成研究．, 第56回日本薬学会第138年会, Mar. 2018.
102.	Hideo Satoh, 林直樹, Atsushi Nakayama, Sangita Karanjit, 小田真隆 and Kosuke Namba : Eurotiumide類の網羅的不斉全合成, 第56回日本薬学会第138年会, Mar. 2018.
103.	Sayaka Sasaki, Haruka Mukaiyama, Daisuke Tsuji, 村田佳子, Sangita Karanjit, Atsushi Nakayama, Kouji Itou and Kosuke Namba : ムギネ酸・鉄錯体取り込みトランスポーター標識プローブの開発, 第56回日本薬学会第138年会, Mar. 2018.
104.	Tsubasa Okamoto, Miki Shibata, Sangita Karanjit, Atsushi Nakayama and Kosuke Namba : [ 4+3 ] 環化付加反応を用いたトロパン骨格効率的構築法の開発, 第56回日本薬学会第138年会, Mar. 2018.
105.	Sangita Karanjit, Masaya Kashihara, Atsushi Nakayama and Kosuke Namba : A Versatile Heterogeneous Pd Nanocluster Catalyst for Bond Transformation under Mild Condition, 日本化学会第98回春季年会, Mar. 2018.
106.	Atsumi Urabe, Ryo Tsugawa, Satoshi Nishio, Sayaka Sasaki, 鈴木基史, 増田寛志, Sangita Karanjit, Atsushi Nakayama, 小林高範 and Kosuke Namba : 鉄取り込み機能を有するムギネ酸類のアルカリ性不良土壌における実用化研究, 日本化学会第98回春季年会, Mar. 2018.
107.	Mai Hamada, Shinichiroh Nakayama, Atsushi Nakayama, Sangita Karanjit and Kosuke Namba : ．LL-Z1640-2を含むResorcylic Acid Lactone類の網羅的合成研究, 第56回日本薬学会・日本薬剤師会・日本病院薬剤師会中国四国支部学術大会, Oct. 2017.
108.	Atsumi Urabe, Ryo Tsugawa, Satoshi Nishio, Sayaka Sasaki, 鈴木基史, Sangita Karanjit, Atsushi Nakayama and Kouji Itou : アルカリ性不良土壌での農耕を志向したムギネ酸類の実用化研究, 第56回日本薬学会・日本薬剤師会・日本病院薬剤師会中国四国支部学術大会, Oct. 2017.
109.	Sayaka Sasaki, Haruka Mukaiyama, Atsumi Urabe, Daisuke Tsuji, 村田佳子, Sangita Karanjit, Atsushi Nakayama, Kouji Itou and Kosuke Namba : 鉄イオン取り込みトランスポーターの標識プローブの開発, 第56回日本薬学会・日本薬剤師会・日本病院薬剤師会中国四国支部学術大会, Oct. 2017.
110.	Tsubasa Okamoto, Sangita Karanjit, Atsushi Nakayama and Kosuke Namba : トロパン骨格効率的構築法の開発, 第56回日本薬学会・日本薬剤師会・日本病院薬剤師会中国四国支部学術大会, Oct. 2017.
111.	Masaya Kashihara, Sangita Karanjit, Atsushi Nakayama and Kosuke Namba : Highly active and stable heterogeneous Pd-Hydrotalcite for Suzuki coupling reaction of artless halides, 第56回日本薬学会・日本薬剤師会・日本病院薬剤師会中国四国支部学術大会, Oct. 2017.
112.	Tsubasa Okamoto, Miki Shibata, Sangita Karanjit, Atsushi Nakayama and Kosuke Namba : トロパン骨格効率的構築法の開発, 第33回若手化学者のための化学道場, Sep. 2017.
113.	Atsumi Urabe, Ryo Tsugawa, Satoshi Nishio, Sayaka Sasaki, 鈴木基史, Sangita Karanjit, Atsushi Nakayama and Kosuke Namba : 第12回トランスポーター研究会年会, Jul. 2017.
114.	Sayaka Sasaki, Haruka Mukaiyama, Atsumi Urabe, Daisuke Tsuji, 村田佳子, Sangita Karanjit, Atsushi Nakayama, Kouji Itou and Kosuke Namba : イネ科植物の鉄イオン取り込みトランスポーターの機構解明に向けた化学プローブの開発, 第12回トランスポーター研究会年会, Jul. 2017.
115.	Atsushi Nakayama, Hideo Satoh, Shinichiroh Nakayama, Sangita Karanjit and Kosuke Namba : サリチル酸系天然物Eurotiumide AとLL-Z1640-2の不斉全合成, 第111回有機合成シンポジウム, Jun. 2017.
116.	Sayaka Sasaki, Ryo Tsugawa, Satoshi Nishio, Haruka Mukaiyama, Atsumi Urabe, 鈴木基史, Atsushi Nakayama, Sangita Karanjit and Kosuke Namba : アルカリ性不良土壌での農耕を指向したムギネ酸類の実用化研究, 日本薬学会第137年会,東北大学, Mar. 2017.
117.	Akane Mera, 小田真隆, Atsushi Nakayama, Sangita Karanjit and Kosuke Namba : 細菌類の迅速同定を目指した蛍光標識vivrioferrinの合成研究, 日本薬学会第137年会,東北大学, Mar. 2017.
118.	Tsubasa Okamoto, Miki Shibata, Atsushi Nakayama, Sangita Karanjit and Kosuke Namba : ピロールの触媒的分子内[4+3]環化付加反応の開発, 日本薬学会第137年会,東北大学, Mar. 2017.

Grants-in-Aid for Scientific Research (KAKEN Grants Database @ NII.ac.jp)

光免疫療法の低分子化への挑戦：超小型赤色光応答性色素の開発と応用 (Project/Area Number: 24K21826 )
Next-generation research on desert greening fertiliezer mugineic acid: Elucidation of the melecular mechanism of mugineic acid utilization by other organisms (Project/Area Number: 22H00352 )
Synthesis of active and stable bifunctional nanocluster catalysts and their application in Carbondioxide insertion reaction (Project/Area Number: 19K15361 )
Elucidation of the molecular mechanism of the innovative fertilizer that greens the desert: unknown function search of phytosiderophore (Project/Area Number: 19H02851 )
Search by Researcher Number (60784650)

Associate Professor : Karanjit, Sangita

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Grants-in-Aid for Scientific Research (KAKEN Grants Database @ NII.ac.jp)