論文発表

Convergent Synthesis of the WXYZA′B′C′D′E′F′ Ring Segment of Maitotoxin
K. Umeno, H. Onoue, K. Konoki, K. Torikai, Y. Yasuno, M. Satake, T. Oishi, Bull. Chem. Soc. Jpn. 2022, 95, 325.

梯子状ポリエーテルの設計・合成・機能解析
大石徹, 高分子 2021, 70, 508.
アンフィジノール3の全合成
若宮佑真，大石徹, 有機合成化学協会誌 2021, 79, 664.
Synthetic Study of the C'D'E' Ring System of Maitotoxin via Furan Based Strategy
Y. Watanabe, K. Torikai, Y. Yasuno, T. Oishi, Heterocycles 2021, 102, 2313.

地道にコツコツと石の上にも十五年　百工程越えの天然物の全合成
大石徹, 化学と工業 2020, 73, 573.
Structure Determination, Chemical Synthesis, and Evaluation of Biological Activity of Super Carbon Chain Natural Products
T. Oishi, Bull. Chem. Soc. Jpn. 2020, 3, 1350.
Synthesis and Stereochemistry of the C30-C63 Section of Karlotoxin 2
K. Umeno, T. Oishi, Asian J. Org. Chem. 2020, 9, 1597.
ホヤの精子活性化誘引物質の化学合成，構造決定，および生物活性評価
土川博史，大石徹, 有機合成化学協会誌 2020, 78, 213.
N(π)-2-Naphthylmethoxymethyl-Protected Histidines: Scalable, Racemization-Free Building Blocks for Peptide Synthesis
K. Torikai, R. Yanagimoto, L. A. Watanabe, Org. Process Res. Dev.
Total Synthesis of Amphidinol 3: A General Strategy for Synthesizing Amphidinol Analogues and Structure-Activity Relationship Study.
Y. Wakamiya, M. Ebine, N. Matsumori, T. Oishi, J. Am. Chem. Soc. 2020, 142, 3472.

Structure-Activity Relationship Studies of Maitotoxin Based on Chemical Synthesis.
T. Oishi, Cutting-Edge Organic Synthesis and Chemical Biology of Bioactive Molecules. The Shape of Organic Synthesis to Come. Chapter 6. pp.125−143. Springer.
Design and Synthesis of Artificial Ladder-Shaped Polyethers for Exploring Biological Functions.
T. Oishi, Heterocycles 2019, 99, 21.
Simple Apparatus for Adding Small Amounts of Powder Materials under an Inert Atmosphere
M. Karak, Y. Joh, K. U. Khodjaniyazov, S. S. Sagdullaev, T. Oishi, K. Torikai, Synlett 2019, 30, 2058.
Unified Synthesis of the DEF and GHI Ring Systems of Maitotoxin
T.Yasudomi, H. Yakushiji, K. Torikai, M. Ebine, T. Oishi, Chem. Lett. 2019, 48, 1156.
1,2-trans Glycosylation via Neighboring Group Participation of 2-O-Alkoxymethyl Groups: Application to One-Pot Oligosaccharide Synthesis
M. Karak, Y. Joh, M. Suenaga, T. Oishi, K. Torikai, Org. Lett. 2019, 21, 1221.

Convergent Syntheses of the WXYZ Ring of Maitotoxin and the HIJK Ring of Brevisulcenal-F
N. Osato, H. Onoue, Y. Toma, K. Torikai, M. Ebine, M. Satake, T. Oishi, Chem. Lett. 2018, 47, 265.
Flow Synthesis of (3R)- and (3S)-(E)-1-Iodohexa-1,5-dien-3-ol: Chiral Building Blocks for Natural Product Synthesis
S. Katayama, T. Koge, S. Katsuragi, S. Akai, T. Oishi, Chem. Lett. 2018, 47, 1116.
Synthesis and Complete Structure Determination of a Sperm-Activating and -Attracting Factor Isolated from the Ascidian Ascidia sydneiensis
T. Watanabe, H. Shibata, M. Ebine, H. Tsuchikawa, N. Matsumori, M. Murata, M. Yoshida, M. Morisawa, S. Lin, K. Yamauchi, K. Sakai, T. Oishi, J. Nat. Prod. 2018, 81, 985.
Synthesis and Stereochemical Revision of the C31-C67 Fragment of Amphidinol 3
Y. Wakamiya, M. Ebine, M. Murayama, H. Omizu, N. Matsumori, T. Oishi, Angew. Chem. Int. Ed. 2018, 57, 6060.
Synthesis of 6/6/6-Ttricyclic Ether System via Achmatowicz and Intramolecular Oxa-Michael Reactions
H. Yamamoto, K. Torikai, M. Ebine, T. Oishi, Heterocycles 2018, 97, 158.
Synthesis of an Analog of Amphidinol 3 Corresponding to the C31-C67 Section
T. Koge, Y. Wakamiya, M. Ebine, T. Oishi, Heterocycles 2018, 96, 1197.
Synthesis of Anti-tubercular Marine Alkaloids Denigrins A and B
M. Karak, T. Oishi, K. Torikai, Tetrahedron Lett. 2018, 59, 2800.

1-Naphthylmethyl and 1-Naphthylmethoxymethyl Protecting Groups: New Members of the Benzyl- and Benzyloxymethyl-type Family
T. Sato, Y. Joh, T. Oishi, K. Torikai, Tetrahedron Lett. 2017, 58, 2178.
Design and Synthesis of Benzoacridines as Estrogenic and Anti-estrogenic Agents
K. Torikai, R. Koga, X. Liu, K. Umehara, T. Kitano, K. Watanabe, T. Oishi, H. Noguchi, Y. Shimohigashi, Bioorg. Med. Chem. 2017, 25, 5216.
Syntheses and Biological Activities of the LMNO, ent-LMNO, and NOPQR(S) Ring Systems of Maitotoxin
H. Onoue, R. Marubayashi, E. Ishikawa. K. Konoki, K. Torikai, M. Ebine, M. Murata, T. Oishi J. Org. Chem. 2017, 82, 9595.
Synthesis of a Truncated Analog of Amphidinol 3 Corresponding to the C21-C39/C52-C67 Section
M. Ebine, Y. Takada, N. Yanai, T. Oishi, Chem. Lett. 2017, 46, 662.

2-Naphthylmethoxymethyl as a Mildly Introducible and Oxidatively Removable Benzyloxymethyl-Type Protecting Group
T. Sato, T. Oishi, K. Torikai, Org. Lett. 2015, 17, 3110.
Stereoselective Synthesis of the C1-C29 Part of Amphidinol 3
T. Tsuruda, M. Ebine, A. Umeda, T. Oishi J. Org. Chem. 2015, 80, 859.
Tuned Classical Thermal Aromatization Furnishing an Estrogenic Benzoacridine
R. Koga, T. Oishi, K. Torikai, Synlett 2015, 26, 2801.

Synthesis and Biological Activity of the C'D'E'F' Ring System of Maitotoxin
M. Kunitake, T. Oshima, K. Konoki. M. Ebine, K. Torikai, M. Murata, T. Oishi J. Org. Chem. 2014, 79, 4948.
Synthesis and biological activity of the QRS ring system of maitotoxin
H. Onoue, T. Baba, K. Konoki, K. Torikai, M. Ebine, T. Oishi Chem. Lett. 2014, 43, 1904.

Synthesis and Structure Revision of the C43-C67 Part of Amphidinol 3
M. Ebine, M. Kanemoto, Y. Manabe, Y. Konno, K. Sakai, N. Matsumori, M. Murata, T. Oishi, Org. Lett. 2013, 15, 2846.

Confirmation of the Absolute Configuration at C45 of Amphidinol 3
Y. Manabe, M. Ebine, N. Matsumori, M. Murata, T. Oishi, J. Nat. Prod. 2012, 75, 2003.