{"id":3746,"date":"2026-03-24T15:45:29","date_gmt":"2026-03-24T06:45:29","guid":{"rendered":"http:\/\/www.iar.nagoya-u.ac.jp\/eng\/?post_type=interviews&#038;p=3746"},"modified":"2026-03-24T17:54:06","modified_gmt":"2026-03-24T08:54:06","slug":"%e3%80%90organic-chemistry%e3%80%91%e3%80%90takashi-ooi%e3%80%91a-researchers-uniqueness-what-have-i-accomplished","status":"publish","type":"interviews","link":"http:\/\/www.iar.nagoya-u.ac.jp\/eng\/publishing\/interviews\/3746\/","title":{"rendered":"\u3010Organic Chemistry\u3011\u3010Takashi OOI\u3011A researcher\u2019s uniqueness\u2014what have I accomplished?"},"content":{"rendered":"<p><img loading=\"lazy\" src=\"http:\/\/www.iar.nagoya-u.ac.jp\/eng\/wp-content\/uploads\/sites\/4\/2026\/03\/1.-DSC_2025_09_17_121055-512x341.jpg\" alt=\"\" width=\"512\" height=\"341\" class=\"alignnone size-medium wp-image-3747\" srcset=\"http:\/\/www.iar.nagoya-u.ac.jp\/eng\/wp-content\/uploads\/sites\/4\/2026\/03\/1.-DSC_2025_09_17_121055-512x341.jpg 512w, http:\/\/www.iar.nagoya-u.ac.jp\/eng\/wp-content\/uploads\/sites\/4\/2026\/03\/1.-DSC_2025_09_17_121055-768x511.jpg 768w, http:\/\/www.iar.nagoya-u.ac.jp\/eng\/wp-content\/uploads\/sites\/4\/2026\/03\/1.-DSC_2025_09_17_121055.jpg 1000w\" sizes=\"(max-width: 512px) 100vw, 512px\" \/><\/p>\n<p><span style=\"font-size: 24pt\"><strong>Takashi OOI<\/strong><\/span> (Ph.D.)<\/p>\n<p>Professor, Institute of Transformative Bio-Molecules, Graduate School of Engineering, Nagoya University<br \/>\n&#8212;<br \/>\nProf. Ooi\u2019s research, centered on organic ion pair catalysis, is unique in the world. Currently conducting research that combines radical reactions as a KAKENHI* recipient project in the category of Transformative Research Areas (A) Green Catalysis Science for Renovating Transformation of Carbon-Based Resources, he continues to communicate new findings in Chemistry to the world.<\/p>\n<p>*The Japan Society for the Promotion of Science (JSPS) Grants-in-Aid for Scientific Research<br \/>\n&#8212;<\/p>\n<p>As an undergraduate student, Prof. Ooi wondered whether he should go on to a doctoral course. Until then, he had been working hard, carrying out experiments day and night and gaining some confidence as a young researcher. Yet, his critical mind had some doubts: The world is vast and filled with diverse people. So would he want to spend the rest of his life in the lab?<\/p>\n<p>He considered the option of a corporate job. As he imagined himself lined up with other students from various universities in an interview room, he wondered why he should be selected and whether he represented something special that would justify a salary. His own answer was, \u201cNot really.\u201d<\/p>\n<p>Although he had achieved some research results by then, he himself had never come up with research ideas from scratch. He thought that he had simply been working hard. In such a situation, his mentor, then Associate Prof. Keiji Maruoka (now Designated Professor, Graduate School of Pharmaceutical Sciences, Kyoto University), suggested that he enter a doctoral program. He felt encouraged, noticing that someone believed, even if only a little, that he should pursue that path.<\/p>\n<p>He imagined himself doing his own research with his own ideas, which he would test in experiments, exploring unknown spheres of Chemistry. He thought about the kind of scientist he wanted to be, someone who would accomplish something unique through teamwork with those with whom he would build a relationship of trust. Yes, I\u2019m going to do a Ph.D., he decided. Since then, he has been asking himself, \u201cIs there something unique only I can do?\u201d<\/p>\n<p><img loading=\"lazy\" src=\"http:\/\/www.iar.nagoya-u.ac.jp\/eng\/wp-content\/uploads\/sites\/4\/2026\/03\/2.-DSC_2025_09_17_111016-512x341.jpg\" alt=\"\" width=\"512\" height=\"341\" class=\"alignnone size-medium wp-image-3748\" srcset=\"http:\/\/www.iar.nagoya-u.ac.jp\/eng\/wp-content\/uploads\/sites\/4\/2026\/03\/2.-DSC_2025_09_17_111016-512x341.jpg 512w, http:\/\/www.iar.nagoya-u.ac.jp\/eng\/wp-content\/uploads\/sites\/4\/2026\/03\/2.-DSC_2025_09_17_111016-768x511.jpg 768w, http:\/\/www.iar.nagoya-u.ac.jp\/eng\/wp-content\/uploads\/sites\/4\/2026\/03\/2.-DSC_2025_09_17_111016.jpg 1000w\" sizes=\"(max-width: 512px) 100vw, 512px\" \/><\/p>\n<p>Looking back on his journey so far, Prof. Ooi says: \u201cTo put it a little dramatically, I think there\u2019s real value in trying something and failing. All the ideas accumulated through each research project that never made it into papers will eventually lead to something, and this is what makes the uniqueness of each researcher.\u201d<\/p>\n<p>What appears in research papers is just the tip of the iceberg. A researcher\u2019s treasure lies in the vast number of experiments and numerous negative data that are behind published results. Prof. Ooi says that relying on efficacy and good ideas is correct in some ways, but he also believes that research results coming solely from them will not stand the test of time.<\/p>\n<p>Prof. Ooi\u2019s experiment-filled life began in his fourth undergraduate year, when he was assigned to a research lab.<\/p>\n<h3>Support from mentors during his experiment-filled days<\/h3>\n<p>He remembers being \u201ca lazy student.\u201d Prof. Hisashi Yamamoto (now Professor Emeritus at Nagoya University) and Prof. Maruoka taught him organic chemistry from scratch and mentored him all along. They played such a major role in his career that he says, \u201cMy meeting with them was the starting point for everything.\u201d When he was a fourth-year undergraduate, a paper he co-authored with them was published in the prestigious American Chemical Society\u2019s journal. It is a memorable paper for him, with his name appearing between his two mentors\u2019 names.<\/p>\n<figure id=\"attachment_3749\" aria-describedby=\"caption-attachment-3749\" style=\"width: 512px\" class=\"wp-caption alignnone\"><img loading=\"lazy\" src=\"http:\/\/www.iar.nagoya-u.ac.jp\/eng\/wp-content\/uploads\/sites\/4\/2026\/03\/72ba97c86ada7ad1ef6615976d1f2864-512x369.jpg\" alt=\"\" width=\"512\" height=\"369\" class=\"size-medium wp-image-3749\" srcset=\"http:\/\/www.iar.nagoya-u.ac.jp\/eng\/wp-content\/uploads\/sites\/4\/2026\/03\/72ba97c86ada7ad1ef6615976d1f2864-512x369.jpg 512w, http:\/\/www.iar.nagoya-u.ac.jp\/eng\/wp-content\/uploads\/sites\/4\/2026\/03\/72ba97c86ada7ad1ef6615976d1f2864-768x554.jpg 768w, http:\/\/www.iar.nagoya-u.ac.jp\/eng\/wp-content\/uploads\/sites\/4\/2026\/03\/72ba97c86ada7ad1ef6615976d1f2864.jpg 788w\" sizes=\"(max-width: 512px) 100vw, 512px\" \/><figcaption id=\"caption-attachment-3749\" class=\"wp-caption-text\">\u201cOrganoaluminum-Promoted Rearrangement of Epoxy Silyl Ethers to \u03b2-Siloxy Aldehydes\u201d Keiji Maruoka, Takashi Ooi, and Hisashi Yamamoto; J. Am. Chem. Soc. 1989, 111, 6431-6432.<\/figcaption><\/figure>\n<p>Compounds, although made of the same material, can be made completely different if shaped differently, even only slightly. As an example, let us take a look at some steps of the experiment that the three researchers conducted in the process of producing results that led to the paper mentioned above. Do you notice in Fig. \u2460 and \u2461 the difference in the shape of the starting materials and in the shape and number of the resulting compounds?<\/p>\n<figure id=\"attachment_3750\" aria-describedby=\"caption-attachment-3750\" style=\"width: 389px\" class=\"wp-caption alignnone\"><img loading=\"lazy\" src=\"http:\/\/www.iar.nagoya-u.ac.jp\/eng\/wp-content\/uploads\/sites\/4\/2026\/03\/058c5cad6922150792ae6efae9e8fe6f-389x512.jpg\" alt=\"\" width=\"389\" height=\"512\" class=\"size-medium wp-image-3750\" srcset=\"http:\/\/www.iar.nagoya-u.ac.jp\/eng\/wp-content\/uploads\/sites\/4\/2026\/03\/058c5cad6922150792ae6efae9e8fe6f-389x512.jpg 389w, http:\/\/www.iar.nagoya-u.ac.jp\/eng\/wp-content\/uploads\/sites\/4\/2026\/03\/058c5cad6922150792ae6efae9e8fe6f-778x1024.jpg 778w, http:\/\/www.iar.nagoya-u.ac.jp\/eng\/wp-content\/uploads\/sites\/4\/2026\/03\/058c5cad6922150792ae6efae9e8fe6f-768x1011.jpg 768w, http:\/\/www.iar.nagoya-u.ac.jp\/eng\/wp-content\/uploads\/sites\/4\/2026\/03\/058c5cad6922150792ae6efae9e8fe6f-1167x1536.jpg 1167w, http:\/\/www.iar.nagoya-u.ac.jp\/eng\/wp-content\/uploads\/sites\/4\/2026\/03\/058c5cad6922150792ae6efae9e8fe6f-1556x2048.jpg 1556w, http:\/\/www.iar.nagoya-u.ac.jp\/eng\/wp-content\/uploads\/sites\/4\/2026\/03\/058c5cad6922150792ae6efae9e8fe6f-scaled.jpg 1945w\" sizes=\"(max-width: 389px) 100vw, 389px\" \/><figcaption id=\"caption-attachment-3750\" class=\"wp-caption-text\">Illustration of a part of an epoxide ring-opening reaction (For clarity, the atomic symbols for hydrogen and the hydrogen atoms in the formyl group in the product are omitted.)<br \/>\nIn both \u2460 and \u2461, the starting material contains 12 carbon atoms (C), 24 hydrogen atoms (H), and one oxygen atom (O), but their configurations differ slightly. Aluminum (Al) in the catalyst coordinates with O. In \u2460, it is unclear which of the two carbon bonds will break, but in \u2461, only the bond on the left carbon is selectively broken.<\/figcaption><\/figure>\n<p>In the very early stage of the experiment, a jumble of many different compounds with seemingly similar yet essentially different structures came about. Then, suddenly one day, it became possible to selectively obtain just one compound. He did not immediately understand how this worked. He was simply surprised by the results and thought, \u201cSomething\u2019s different.\u201d<\/p>\n<figure id=\"attachment_3751\" aria-describedby=\"caption-attachment-3751\" style=\"width: 512px\" class=\"wp-caption alignnone\"><img loading=\"lazy\" src=\"http:\/\/www.iar.nagoya-u.ac.jp\/eng\/wp-content\/uploads\/sites\/4\/2026\/03\/5.-DSC_2025_09_17_115000-512x341.jpg\" alt=\"\" width=\"512\" height=\"341\" class=\"size-medium wp-image-3751\" srcset=\"http:\/\/www.iar.nagoya-u.ac.jp\/eng\/wp-content\/uploads\/sites\/4\/2026\/03\/5.-DSC_2025_09_17_115000-512x341.jpg 512w, http:\/\/www.iar.nagoya-u.ac.jp\/eng\/wp-content\/uploads\/sites\/4\/2026\/03\/5.-DSC_2025_09_17_115000-768x511.jpg 768w, http:\/\/www.iar.nagoya-u.ac.jp\/eng\/wp-content\/uploads\/sites\/4\/2026\/03\/5.-DSC_2025_09_17_115000.jpg 1000w\" sizes=\"(max-width: 512px) 100vw, 512px\" \/><figcaption id=\"caption-attachment-3751\" class=\"wp-caption-text\">Prof. Ooi\u2019s lab notebook from that time: The details of the experiment are recorded carefully on each page; the first neat synthesis of the compound is described on the page on the right in the photo.<\/figcaption><\/figure>\n<p>At first, Prof. Yamamoto advised a young Mr. Ooi to change his attitude. Prof. Maruoka often gave him an earful as they spent all their time in the lab. Gradually, however, he began to find experiments more interesting. Preparation for the graduate school entrance exam was the first time he studied seriously since entering university. His hard work to stay in the lab as a graduate student resulted in excellent grades. Prof. Maruoka was pleasantly surprised. Prof. Yamamoto also sensed the change in Mr. Ooi. When he was in his second year of graduate school, Prof. Yamamoto personally assigned him to tutoring some younger students. He still treasures the moment he was given this task.<\/p>\n<p>\u201cFor Prof. Yamamoto, it may have been nothing special, but it made me very happy,\u201d says Prof. Ooi.<\/p>\n<p><img loading=\"lazy\" src=\"http:\/\/www.iar.nagoya-u.ac.jp\/eng\/wp-content\/uploads\/sites\/4\/2026\/03\/6.-DSC_2025_09_17_104400-512x341.jpg\" alt=\"\" width=\"512\" height=\"341\" class=\"alignnone size-medium wp-image-3752\" srcset=\"http:\/\/www.iar.nagoya-u.ac.jp\/eng\/wp-content\/uploads\/sites\/4\/2026\/03\/6.-DSC_2025_09_17_104400-512x341.jpg 512w, http:\/\/www.iar.nagoya-u.ac.jp\/eng\/wp-content\/uploads\/sites\/4\/2026\/03\/6.-DSC_2025_09_17_104400-768x511.jpg 768w, http:\/\/www.iar.nagoya-u.ac.jp\/eng\/wp-content\/uploads\/sites\/4\/2026\/03\/6.-DSC_2025_09_17_104400.jpg 1000w\" sizes=\"(max-width: 512px) 100vw, 512px\" \/><\/p>\n<h3>Capturing opportunities while working with lab members<\/h3>\n<p>Prof. Ooi continued to work on many research projects with Prof. Maruoka, who provided him with the opportunity to work as an assistant professor at Hokkaido University and an associate professor at Kyoto University. They also worked together in opening new laboratories and exploring new research topics of chemistry. By that time, Prof. Maruoka had come to treat his mentee as a fellow researcher.<\/p>\n<p>\u201cI was fortunate to be able to work while imagining what Prof. Maruoka was thinking in real-life situations as a scientist,\u201d says Prof. Ooi.<\/p>\n<p>When Prof. Ooi opened his own laboratory at Nagoya University, he started with absolutely nothing but was at ease. His policy was to take advantage of the opportunity he was given and simply do what he wanted to do. He was joined by Dr. Daisuke Uraguchi (then assistant professor, now Professor at Hokkaido University Institute for Catalysis) and five students who chose the laboratory as their first choice. Having such good members was the best driving force for Prof. Ooi and the laboratory.<\/p>\n<p>One day, Prof. Ooi decided to start \u201csomething new,\u201d and he began working on catalytic chemistry of organic ion pairs. One of the lab\u2019s research achievements, which fully utilized Prof. Uraguchi\u2019s area of expertise, was aminophosphonium salt. To briefly explain just a few of the characteristics of this catalyst, it uses the attractive forces between positive and negative charges, the power of hydrogen bonds, and the three-dimensional structure of the catalyst to capture and control starting-material molecules, realizing the selective chemical synthesis of products with a desired structure.<\/p>\n<p><img loading=\"lazy\" src=\"http:\/\/www.iar.nagoya-u.ac.jp\/eng\/wp-content\/uploads\/sites\/4\/2026\/03\/7.-AP-1-rev-512x382.jpg\" alt=\"\" width=\"512\" height=\"382\" class=\"alignnone size-medium wp-image-3753\" srcset=\"http:\/\/www.iar.nagoya-u.ac.jp\/eng\/wp-content\/uploads\/sites\/4\/2026\/03\/7.-AP-1-rev-512x382.jpg 512w, http:\/\/www.iar.nagoya-u.ac.jp\/eng\/wp-content\/uploads\/sites\/4\/2026\/03\/7.-AP-1-rev-768x573.jpg 768w, http:\/\/www.iar.nagoya-u.ac.jp\/eng\/wp-content\/uploads\/sites\/4\/2026\/03\/7.-AP-1-rev.jpg 826w\" sizes=\"(max-width: 512px) 100vw, 512px\" \/> <img loading=\"lazy\" src=\"http:\/\/www.iar.nagoya-u.ac.jp\/eng\/wp-content\/uploads\/sites\/4\/2026\/03\/8.-AP-1-X-512x299.jpg\" alt=\"\" width=\"512\" height=\"299\" class=\"alignnone size-medium wp-image-3754\" srcset=\"http:\/\/www.iar.nagoya-u.ac.jp\/eng\/wp-content\/uploads\/sites\/4\/2026\/03\/8.-AP-1-X-512x299.jpg 512w, http:\/\/www.iar.nagoya-u.ac.jp\/eng\/wp-content\/uploads\/sites\/4\/2026\/03\/8.-AP-1-X-1024x599.jpg 1024w, http:\/\/www.iar.nagoya-u.ac.jp\/eng\/wp-content\/uploads\/sites\/4\/2026\/03\/8.-AP-1-X-768x449.jpg 768w, http:\/\/www.iar.nagoya-u.ac.jp\/eng\/wp-content\/uploads\/sites\/4\/2026\/03\/8.-AP-1-X-1536x898.jpg 1536w, http:\/\/www.iar.nagoya-u.ac.jp\/eng\/wp-content\/uploads\/sites\/4\/2026\/03\/8.-AP-1-X.jpg 1715w\" sizes=\"(max-width: 512px) 100vw, 512px\" \/> <img loading=\"lazy\" src=\"http:\/\/www.iar.nagoya-u.ac.jp\/eng\/wp-content\/uploads\/sites\/4\/2026\/03\/9.-TS-512x499.jpg\" alt=\"\" width=\"512\" height=\"499\" class=\"alignnone size-medium wp-image-3755\" srcset=\"http:\/\/www.iar.nagoya-u.ac.jp\/eng\/wp-content\/uploads\/sites\/4\/2026\/03\/9.-TS-512x499.jpg 512w, http:\/\/www.iar.nagoya-u.ac.jp\/eng\/wp-content\/uploads\/sites\/4\/2026\/03\/9.-TS-768x748.jpg 768w, http:\/\/www.iar.nagoya-u.ac.jp\/eng\/wp-content\/uploads\/sites\/4\/2026\/03\/9.-TS.jpg 808w\" sizes=\"(max-width: 512px) 100vw, 512px\" \/><\/p>\n<p><span style=\"font-size: 10pt;color: #808080\">(Top) A form of aminophosphonium salt, which takes on various shapes; positively charged catalyst molecule attracts negatively charged molecules and captures them at the site of hydrogen bonding. In this form, a Cl<sup>&#8211; <\/sup>(chloride ion) is attached.<\/span><\/p>\n<p><span style=\"font-size: 10pt;color: #808080\">(Middle) A three-dimensional structure determined by X-ray structural analysis; it has a compact structure, but it wraps around and fixes the molecule.<\/span><\/p>\n<p><span style=\"font-size: 10pt;color: #808080\">(Bottom) An example of how a catalyst works; reaction is controlled where Cl<sup>&#8211;<\/sup> was attached. For greater detail, refer to the paper below:<\/span><\/p>\n<p><span style=\"font-size: 10pt;color: #808080\">Chiral Tetraaminophosphonium Salt-Mediated Asymmetric Direct Henry Reaction; Daisuke Uraguchi, Sawako Sakaki, and Takashi Ooi; <em>J. Am. Chem. Soc.\u00a0<\/em>2007<em>, 129,\u00a0<\/em>12392-12393.<\/span><\/p>\n<p>This catalyst was further developed thanks to great efforts by the lab\u2019s student. He explored the possibility of replacing the Cl<sup>&#8211;<\/sup> site with another interesting molecule and, starting from scratch, chose phenol, which is readily available in a wide variety of commercial forms.<\/p>\n<figure id=\"attachment_3756\" aria-describedby=\"caption-attachment-3756\" style=\"width: 512px\" class=\"wp-caption alignnone\"><img loading=\"lazy\" src=\"http:\/\/www.iar.nagoya-u.ac.jp\/eng\/wp-content\/uploads\/sites\/4\/2026\/03\/10.-IM-Phe-512x183.jpg\" alt=\"\" width=\"512\" height=\"183\" class=\"size-medium wp-image-3756\" srcset=\"http:\/\/www.iar.nagoya-u.ac.jp\/eng\/wp-content\/uploads\/sites\/4\/2026\/03\/10.-IM-Phe-512x183.jpg 512w, http:\/\/www.iar.nagoya-u.ac.jp\/eng\/wp-content\/uploads\/sites\/4\/2026\/03\/10.-IM-Phe-1024x365.jpg 1024w, http:\/\/www.iar.nagoya-u.ac.jp\/eng\/wp-content\/uploads\/sites\/4\/2026\/03\/10.-IM-Phe-768x274.jpg 768w, http:\/\/www.iar.nagoya-u.ac.jp\/eng\/wp-content\/uploads\/sites\/4\/2026\/03\/10.-IM-Phe.jpg 1133w\" sizes=\"(max-width: 512px) 100vw, 512px\" \/><figcaption id=\"caption-attachment-3756\" class=\"wp-caption-text\">Iminophosphorane, the conjugate base of aminophosphonium and phenol<\/figcaption><\/figure>\n<p>At first, they imagined a structure in which one aminophosphonium was attached to one phenol. The synthesis reaction went reasonably well. However, they were not able to explain why replacement with phenol was necessary. Then one day, the student in charge of this experiment came up with the idea of trying X-ray structural analysis, which revealed a surprising molecular structure. It turned out that there was not just one phenol but two more in between. This gave birth to new three-dimensional structures and made it possible to add various other ingenuities, such as attaching Cl to the phenol.<\/p>\n<p><img loading=\"lazy\" src=\"http:\/\/www.iar.nagoya-u.ac.jp\/eng\/wp-content\/uploads\/sites\/4\/2026\/03\/11.-IM-3Phe-415x512.jpg\" alt=\"\" width=\"415\" height=\"512\" class=\"alignnone size-medium wp-image-3757\" srcset=\"http:\/\/www.iar.nagoya-u.ac.jp\/eng\/wp-content\/uploads\/sites\/4\/2026\/03\/11.-IM-3Phe-415x512.jpg 415w, http:\/\/www.iar.nagoya-u.ac.jp\/eng\/wp-content\/uploads\/sites\/4\/2026\/03\/11.-IM-3Phe-768x948.jpg 768w, http:\/\/www.iar.nagoya-u.ac.jp\/eng\/wp-content\/uploads\/sites\/4\/2026\/03\/11.-IM-3Phe.jpg 790w\" sizes=\"(max-width: 415px) 100vw, 415px\" \/> <img loading=\"lazy\" src=\"http:\/\/www.iar.nagoya-u.ac.jp\/eng\/wp-content\/uploads\/sites\/4\/2026\/03\/12.-IM-3ClPhe-500x512.jpg\" alt=\"\" width=\"500\" height=\"512\" class=\"alignnone size-medium wp-image-3758\" srcset=\"http:\/\/www.iar.nagoya-u.ac.jp\/eng\/wp-content\/uploads\/sites\/4\/2026\/03\/12.-IM-3ClPhe-500x512.jpg 500w, http:\/\/www.iar.nagoya-u.ac.jp\/eng\/wp-content\/uploads\/sites\/4\/2026\/03\/12.-IM-3ClPhe-768x786.jpg 768w, http:\/\/www.iar.nagoya-u.ac.jp\/eng\/wp-content\/uploads\/sites\/4\/2026\/03\/12.-IM-3ClPhe.jpg 970w\" sizes=\"(max-width: 500px) 100vw, 500px\" \/><\/p>\n<p><span style=\"font-size: 10pt;color: #808080\">(Top) Aminophosphonium with three phenol molecules attached<\/span><\/p>\n<p><span style=\"font-size: 10pt;color: #808080\">(Bottom) Rearrangements with substituents on aminophosphonium and phenol molecules enabling further improvement on catalyst<\/span><\/p>\n<p>The scientists often made a breakthrough by accident. It was serendipity in action. Their paper was published in <em>Science<\/em>, where the student\u2019s name appeared between the names of his two supervisors. The story of young Mr. Ooi was repeated.<\/p>\n<figure id=\"attachment_3759\" aria-describedby=\"caption-attachment-3759\" style=\"width: 512px\" class=\"wp-caption alignnone\"><img loading=\"lazy\" src=\"http:\/\/www.iar.nagoya-u.ac.jp\/eng\/wp-content\/uploads\/sites\/4\/2026\/03\/18e183289c2584ad401362ff1b454cb5-512x274.jpg\" alt=\"\" width=\"512\" height=\"274\" class=\"size-medium wp-image-3759\" srcset=\"http:\/\/www.iar.nagoya-u.ac.jp\/eng\/wp-content\/uploads\/sites\/4\/2026\/03\/18e183289c2584ad401362ff1b454cb5-512x274.jpg 512w, http:\/\/www.iar.nagoya-u.ac.jp\/eng\/wp-content\/uploads\/sites\/4\/2026\/03\/18e183289c2584ad401362ff1b454cb5-1024x548.jpg 1024w, http:\/\/www.iar.nagoya-u.ac.jp\/eng\/wp-content\/uploads\/sites\/4\/2026\/03\/18e183289c2584ad401362ff1b454cb5-768x411.jpg 768w, http:\/\/www.iar.nagoya-u.ac.jp\/eng\/wp-content\/uploads\/sites\/4\/2026\/03\/18e183289c2584ad401362ff1b454cb5.jpg 1076w\" sizes=\"(max-width: 512px) 100vw, 512px\" \/><figcaption id=\"caption-attachment-3759\" class=\"wp-caption-text\">Chiral Organic Ion Pair Catalysts Assembled Through a Hydrogen-Bonding Network; Daisuke Uraguchi, Yusuke Ueki, Takashi Ooi; Science. 2009, 326, 120-123.<\/figcaption><\/figure>\n<h3>Encounters with people and repeated experiments leading to new chemistry<\/h3>\n<p>When Prof. Ooi takes on a new challenge, there is no hesitation. Even if successful outcomes seem unlikely, he forges ahead with his teammates on a project, as long as it has inherent originality.<\/p>\n<p>\u201cIt\u2019s not about whether there\u2019s hope ahead. It\u2019s about whether you do it or not. In the dark, taking a step forward brings about a ray of hope.\u201d<\/p>\n<p>Prof. Ooi has been supported by many people and given opportunities. Building on the foundation of numerous experiments he has conducted with the lab members, he simply continues in pursuit of something unique that only he can do.<\/p>\n<p>\u201cI am hoping to do the kind of research in chemistry that makes people around the world think and say, \u2018Isn\u2019t this from Ooi\u2019s lab?\u2019 even if the findings are published without the authors\u2019 names or university name.\u201d<\/p>\n<p>(Interview and Text: Tatsuro AYATSUKA, Interview Date: September 17, 2025)<\/p>\n","protected":false},"featured_media":3747,"template":"","performance_cat":[],"performance_tag":[],"acf":[],"_links":{"self":[{"href":"http:\/\/www.iar.nagoya-u.ac.jp\/eng\/wp-json\/wp\/v2\/interviews\/3746"}],"collection":[{"href":"http:\/\/www.iar.nagoya-u.ac.jp\/eng\/wp-json\/wp\/v2\/interviews"}],"about":[{"href":"http:\/\/www.iar.nagoya-u.ac.jp\/eng\/wp-json\/wp\/v2\/types\/interviews"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.iar.nagoya-u.ac.jp\/eng\/wp-json\/wp\/v2\/media\/3747"}],"wp:attachment":[{"href":"http:\/\/www.iar.nagoya-u.ac.jp\/eng\/wp-json\/wp\/v2\/media?parent=3746"}],"wp:term":[{"taxonomy":"performance_cat","embeddable":true,"href":"http:\/\/www.iar.nagoya-u.ac.jp\/eng\/wp-json\/wp\/v2\/performance_cat?post=3746"},{"taxonomy":"performance_tag","embeddable":true,"href":"http:\/\/www.iar.nagoya-u.ac.jp\/eng\/wp-json\/wp\/v2\/performance_tag?post=3746"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}