研究者基本情報

• 博士（理学）, シェフィールド大学, 2014年01月

• https://researchmap.jp/jjiang1988

• https://jglobal.jst.go.jp/detail?JGLOBAL_ID=202001007556819514

• 202001007556819514

• Computational Chemistry
• Radical Chemistry
• Homogeneous Catalysis
• Physical Organic Chemistry

• 情報通信, 計算科学
• ナノテク・材料, 構造有機化学、物理有機化学

• 修士課程, 総合化学院
• 博士課程, 総合化学院

研究活動情報

• Breaking the Immiscibility Barrier: A Mechanochemical Approach to Enable the Direct Glycosylation of Native Sugars with Hydrophobic Aliphatic Alcohols
  Koji Kubota; Yuri Kamakura; Taiga Takeda; Julong Jiang; Yoshiyuki Manabe; Koichi Fukase; Hajime Ito
  Journal of the American Chemical Society, American Chemical Society (ACS), 2026年05月05日, ［査読有り］
  研究論文（学術雑誌）
• Rh‐Catalyzed Chemodivergent Parallel Kinetic Resolution and Desymmetrization of Enynes and Dienynes with Acrylamides
  Shintaro Hamada; Julong Jiang; Yu Sato; Takashi Yamazaki; Satoshi Maeda; Ken Tanaka
  Angewandte Chemie International Edition, 65, 17, Wiley, 2026年03月15日, ［査読有り］
  研究論文（学術雑誌）, ABSTRACT
  
  Catalytic enantioselective synthesis of structurally diverse 3D molecules remains a central challenge in organic chemistry. Intermolecular chemodivergent parallel kinetic resolution (PKR) of racemic substrates through C─C bond formation using a single catalyst to yield distinct products is rare. Here, we report Rh‐catalyzed chemodivergent PKR of racemic 1,6‐enynes with α‐fluoroacrylamides or mixtures of different acrylamides, proceeding via [2+2+2] cycloaddition and C–H alkylation to afford structurally and stereochemically distinct products with high selectivity under mild conditions. Additionally, substituent‐dependent enantioselective desymmetrization of symmetric dienynes was achieved. Computational studies revealed that, depending on the stereochemistry of the 1,6‐enyne, steric repulsion between the ligand and the enyne favors a compact C–H activation transition state, whereas its absence favors a C═C insertion transition state involving a smaller bond dissociation energy. These findings establish a versatile catalytic platform for the selective generation of 3D molecular complexity, advancing diversity‐oriented synthesis from racemic or symmetric precursors.
• Using Mechanochemistry to Activate Poly(vinyl chloride) as a Mechanotunable Brønsted-Acid-Releasing Reagent for Organic Synthesis
  Koji Kubota; Reon Hisazumi; Kalipada Jana; Julong Jiang; Tsubura Endo; Satoshi Maeda; Hajime Ito
  Journal of the American Chemical Society, American Chemical Society (ACS), 2026年01月02日, ［査読有り］
  研究論文（学術雑誌）
• Computational Exploration of Polymer Mechanochemistry: Quantitation of Activation Force and Systematic Discovery of Reaction Sites by the Extended Artificial Force-Induced Reaction Method
  Julong Jiang; Koji Kubota; Yu Harabuchi; Mingoo Jin; Zhi Jian Wang; Tasuku Nakajima; Hajime Ito; Jian Ping Gong; Satoshi Maeda
  Journal of the American Chemical Society, American Chemical Society (ACS), 2025年08月29日, ［査読有り］
  研究論文（学術雑誌）
• "Node" facilitated thermostable mechanophores for rapid self-strengthening in double network materials.
  Julong Jiang; Zhi Jian Wang; Ruben Staub; Yu Harabuchi; Alexandre Varnek; Jian Ping Gong; Satoshi Maeda
  Chemical science, 2025年07月10日, ［査読有り］, ［国際誌］
  英語, 研究論文（学術雑誌）, Mechanophores are force-sensitive compounds that undergo chemical reactions under force stimuli. The design and discovery of efficient yet thermally stable mechanophores are crucial for developing self-strengthening materials. However, conventional mechanophores are often chemically unstable due to the presence of highly strained rings or weak covalent bonds, making the material sensitive to the change of temperature or UV irradiation. In this study, a comprehensive computational exploration was conducted to discover thermally stable, unconventional mechanophores for self-strengthening materials based on mechanoradical polymerisation. Notably, the computational procedure presented here serves as a general strategy for designing mechanophores intended for various applications. First, a conformational motif called a "node" along the force transduction direction was identified, significantly enhancing the force effect. Molecules with bridged rings emerged as ideal candidates for possessing a "node," as the bridged structure helps to fix the key dihedral angle. Simulations predicted that polymers containing camphanediol and pinanediol could readily undergo C-C bond homolysis under force. Subsequently, automated reaction path exploration revealed the fate of the mechanoradicals and suggested that camphanediol could generate long-lived radicals, a crucial feature for self-strengthening materials. Following these computational predictions, we successfully prepared double-network hydrogels containing the camphanediol moiety. Careful experiments were then performed to quantify the concentration of mechanoradicals, and enhanced self-strengthening performance was demonstrated through loading-unloading tests.
• Introducing Steric Bulk Into Silylboranes: Enhanced Bench Stability and Novel Chemical Reactivity.
  Rikuro Takahashi; Julong Jiang; Satoshi Maeda; Hajime Ito
  Angewandte Chemie (International ed. in English), e202506194, 2025年06月23日, ［査読有り］, ［国際誌］
  英語, 研究論文（学術雑誌）, Silylboranes are versatile intermediates in organic synthesis, and a wide range of structural variants of silylboranes have already been synthesized. However, the stability of silylboranes varies significantly, and their decomposition mechanism remains to be fully understood. Moreover, some silylborane motifs have not yet been applied as synthetic reagents due to their instability. To address this issue, we first investigated the decomposition mechanism of silylboranes in air and moisture using experimental and theoretical methods. We discovered that oxygenation by atmospheric oxygen is the major decomposition pathway, resulting in the formation of a borylsilylether, and that the introduction of a bulky silyl group suppresses this decomposition. Based on these results, we synthesized triisopropylsilyldimesitylborane (i-Pr3Si-BMes2), which exhibits high bench stability. Moreover, i-Pr3Si-BMes2 reacts with carbon monoxide (CO), which is the first example of a reaction between a silylborane and CO. Further computational studies revealed that electronic effects, including hyperconjugation between the Si─B σ-bond and C─O π*-bond, are crucial for CO activation. Furthermore, we prepared a bench-stable bissilylaminoborane by introducing triisopropylsilyl groups, providing a bissilylchloroborane upon hydrogen chloride treatment. These findings provide valuable insights into how steric and electronic effects can be used to optimize the balance between stability and reactivity in silylboranes.
• A Cooperative Electron-Deficient Phosphine/Olefin Ligand System for the Site-Selective Mechanochemical Suzuki–Miyaura Cross-Coupling of 2,4-Dibromoaryl Ethers
  Yunpeng Gao; Julong Jiang; Satoshi Maeda; Koji Kubota; Hajime Ito
  Chemical Science, Royal Society of Chemistry (RSC), 2025年, ［査読有り］
  研究論文（学術雑誌）, The palladium-catalyzed site-selective cross-coupling of identical halogen groups with minimal electronic and steric bias remains a formidable challenge, especially for simple benzene derivatives. Here, we report a cooperative phosphine/olefin ligand...
• Direct Arylation of gem-Difluorostyrenes Using in Situ Mechanochemically Generated Calcium-Based Heavy Grignard Reagents
  Xihong Wang; Yamato Fukuzawa; Pan Gao; Julong Jiang; Satoshi Maeda; Koji Kubota; Hajime Ito
  RSC Mechanochemistry, Royal Society of Chemistry (RSC), 2025年, ［査読有り］
  研究論文（学術雑誌）, In this study, we disclosed that calcium-based heavy Grignard reagents, prepared in situ through a mechanochemical method, reacted with gem-difluorostyrenes in the absence of transition-metal catalysts to afford thermodynamically less...
• Theory-driven Discovery of Thermally Stable Mechanophore for Self-strengthening Materials
  Julong Jiang; Zhi Jian Wang; Ruben Staub; Yu Harabuchi; Alexandre Varnek; Jian Ping Gong; Satoshi Maeda
  American Chemical Society (ACS), 2024年11月13日
  Mechanophores that readily undergo bond cleavage upon mechanical stimuli normally contain a highly strained ring or reactive unit with weak bonds, which are usually thermally unstable. Here, we propose a general theory-driven procedure for selecting thermally stable radical-type mechanophore which can be used in self-strengthening materials. First, following our previous work, it is confirmed that a conformational motif called “node” along the force transduction direction enhances the force effect by generating a severe distortion on the breaking covalent bond. Molecules possessing bridged rings are ideal candidates to have a “node”, as the bridged structure helps to fix the key dihedral angle. Our computational exploration then focused on camphanediol and pinanediol, which do not have highly strained ring or intrinsically weak covalent bond, but a node ensured by a small dihedral angle. Our simulations predicted that polymer chains including these molecular skeletons easily undergo a C−C bond homolysis under relatively low tensile force and efficiently generate mechanoradicals. Subsequently, our automated reaction path exploration calculations unveiled the fate of the mechanoradicals by enumerating their possible reaction channels, and suggested that camphanediol can generate long-lived radicals, which can be utilized to develop self-strengthening materials. Therefore, we prepared double-network (DN) hydrogels containing camphanediol moiety and found that these novel DN hydrogels do have a good self-strengthening performance. Moreover, thanks to the present design guideline not assuming strained rings or weak bonds, such a camphanediol-containing DN hydrogel showed a good thermal and UV stability.
• Mechanochemical Generation of Aryl Barium Nucleophiles from Unactivated Barium Metal
  Koji Kubota; Sota Kawamura; Julong Jiang; Satoshi Maeda; Hajime Ito
  Chemical Science, Royal Society of Chemistry (RSC), 2024年10月, ［査読有り］
  研究論文（学術雑誌）, Organobarium reagents are of interest as homologues of the Grignard reagents based on organomagnesium compounds due to their unique reactivity as well as regio- and stereoselectivity. However, reactions involving organobarium...
• Accessing a Diverse Set of Functional Red-Light Photoswitches by Selective Copper-Catalyzed Indigo N-Arylation
  Amit K. Jaiswal; Priya Saha; Julong Jiang; Kimichi Suzuki; Anna Jasny; Bernd M. Schmidt; Satoshi Maeda; Stefan Hecht; Chung-Yang Dennis Huang
  Journal of the American Chemical Society, 146, 31, 21367, 21376, American Chemical Society (ACS), 2024年07月26日, ［査読有り］
  研究論文（学術雑誌）
• Effect of the Activation Force of Mechanophore on Its Activation Selectivity and Efficiency in Polymer Networks
  Zhi Jian Wang; Shu Wang; Julong Jiang; Yixin Hu; Tasuku Nakajima; Satoshi Maeda; Stephen L. Craig; Jian Ping Gong
  Journal of the American Chemical Society, 146, 19, 13336, 13346, American Chemical Society (ACS), 2024年05月02日, ［査読有り］
  研究論文（学術雑誌）
• Ring Expansion of Cyclic Boronates via Oxyboration of Arynes
  Yuma Shiratori; Julong Jiang; Koji Kubota; Satoshi Maeda; Hajime Ito
  Journal of the American Chemical Society, American Chemical Society (ACS), 2024年01月10日, ［査読有り］
  研究論文（学術雑誌）
• Direct arylation of alkyl fluorides using in situ mechanochemically generated calcium-based heavy Grignard reagents
  Pan Gao; Julong Jiang; Yamato Fukuzawa; Satoshi Maeda; Koji Kubota; Hajime Ito
  RSC Mechanochemistry, Royal Society of Chemistry (RSC), 2024年, ［査読有り］
  研究論文（学術雑誌）, Here, we report the reaction of calcium-based heavy Grignard reagents, which are easily generated by a mechanochemical method, with unactivated alkyl fluorides in the absence of transition metal catalysts to...
• Using Mechanochemistry to Activate Commodity Plastics as Initiators for Radical Chain Reactions of Small Organic Molecules
  Koji Kubota; Julong Jiang; Yuri Kamakura; Reon Hisazumi; Tsubura Endo; Daiyo Miura; Shotaro Kubo; Satoshi Maeda; Hajime Ito
  Journal of the American Chemical Society, American Chemical Society (ACS), 2023年12月22日, ［査読有り］
  研究論文（学術雑誌）
• Azobenzene as a photoswitchable mechanophore
  Yiran Li; Bin Xue; Jiahui Yang; Julong Jiang; Jing Liu; Yanyan Zhou; Junsheng Zhang; Mengjiao Wu; Yuan Yuan; Zhenshu Zhu; Zhi Jian Wang; Yulan Chen; Yu Harabuchi; Tasuku Nakajima; Wei Wang; Satoshi Maeda; Jian Ping Gong; Yi Cao
  Nature Chemistry, Springer Science and Business Media LLC, 2023年12月05日, ［査読有り］
  研究論文（学術雑誌）
• Stereospecific synthesis of silicon-stereogenic optically active silylboranes and general synthesis of chiral silyl anions
  Xihong Wang; Chi Feng; Julong Jiang; Satoshi Maeda; Koji Kubota; Hajime Ito
  Nature Communications, 2023年09月, ［査読有り］
• In Situ and Real-Time Visualization of Mechanochemical Damage in Double-Network Hydrogels by Prefluorescent Probe via Oxygen-Relayed Radical Trapping.
  Yong Zheng; Julong Jiang; Mingoo Jin; Daiyo Miura; Fei Xue Lu; Koji Kubota; Tasuku Nakajima; Satoshi Maeda; Hajime Ito; Jian Ping Gong
  Journal of the American Chemical Society, 2023年03月23日, ［査読有り］, ［国際誌］
  英語, 研究論文（学術雑誌）, Visualization of mechanochemical damages, especially for those in the molecular-scale (e.g., bond scission in polymeric materials), is of great industrial and academic significance. Herein, we report a novel strategy for in situ and real-time visualization of mechanochemical damages in hydrogels by utilizing prefluorescent probes via oxygen-relayed free-radical trapping. Double-network (DN) hydrogels that generate numerous mechanoradicals by homolytic bond scission of the brittle first network at large deformation are used as model materials. Theoretical calculation suggests that mechanoradicals generated by the damage of the first network undergo an oxygen-relayed radical-transfer process which can be detected by the prefluorescent probe through the radical-radical coupling reaction. Such an oxygen-relayed radical-trapping process of the prefluorescent probe exhibits a dramatically enhanced emission, which enables the real-time sensing and visualization of mechanochemical damages in DN hydrogels made from brittle networks of varied chemical structures. To the best of authors' knowledge, this work is the first report utilizing oxygen as a radical-relaying molecule for visualizing mechanoradical damages in polymer materials. Moreover, this new method based on the probe post-loading is simple and does not introduce any chemical structural changes in the materials, outperforming most previous methods that require chemical incorporation of mechanophores into polymer networks.
• Computational Exploration of Polymer Mechanochemistry: Quantitation of Activation Force and Systematic Discovery of Reaction Sites Utilizing Two Forces
  Julong Jiang; Koji Kubota; Mingoo Jin; Zhi Jian Wang; Tasuku Nakajima; Hajime Ito; Jian Ping Gong; Satoshi Maeda
  American Chemical Society (ACS), 2022年11月23日
  A series of mechanophores were studied computationally by employing the AFIR (Artificial Force Induced Reaction) method, which applies an artificial force on the molecule to trigger reactions, and meanwhile with a tensile force to simulate a mechanochemical reaction. The calculation results were both qualitatively and quantitatively consistent to those reported experimentally, indicating that the AFIR is a reliable approach to studying mechanochemical reactions. It was then applied to the study of retro-Diels-Alder reactions for the theoretical predictions of activation force levels which are currently unavailable. Moreover, it also helped to reveal the favored geometry for the enhancement of force effect. Later, the AFIR method was employed to study the mechanodegradation of generic polymers. The substituents effect and the polymer tacticity in strengthening the mechanical responsiveness, were highlighted by our study. Given the importance of cross-linker molecules in the double-network (DN) hydrogels, a fully automatic search of mechanochemical transformation pathways of a commonly used cross-linker molecule, N,N'-methylenebisacrylamide (MBAA), was also performed by the AFIR method. Through the work described in this article, we demonstrated that, in the field of polymer mechanochemistry, the AFIR method utilizing two forces is a simple but effective tool to give accurate predictions of activation force levels at any given timescale. In the meantime, the mechanistic study of mechanochemical reactions shown in this article is believed to provide insightful suggestions for the further design and application of mechanophores.
• Mechanochemically Generated Calcium‐Based Heavy Grignard Reagents and Their Application to Carbon−Carbon Bond‐Forming Reactions
  Pan Gao; Julong Jiang; Satoshi Maeda; Koji Kubota; Hajime Ito
  Angewandte Chemie International Edition, 61, 41, Wiley, 2022年07月19日, ［査読有り］
  研究論文（学術雑誌）
• Azo-Crosslinked Double-Network Hydrogels Enabling Highly Efficient Mechanoradical Generation
  Zhi Jian Wang; Julong Jiang; Qifeng Mu; Satoshi Maeda; Tasuku Nakajima; Jian Ping Gong
  Journal of the American Chemical Society, American Chemical Society (ACS), 2022年02月11日, ［査読有り］
  研究論文（学術雑誌）
• Mechanochemical synthesis of magnesium-based carbon nucleophiles in air and their use in organic synthesis
  Rina Takahashi; Anqi Hu; Pan Gao; Yunpeng Gao; Yadong Pang; Tamae Seo; Julong Jiang; Satoshi Maeda; Hikaru Takaya; Koji Kubota; Hajime Ito
  Nature Communications, 12, 1, Springer Science and Business Media LLC, 2021年12月, ［査読有り］
  研究論文（学術雑誌）, Since the discovery of Grignard reagents in 1900, the nucleophilic addition of magnesium-based carbon nucleophiles to various electrophiles has become one of the most powerful, versatile, and well-established methods for the formation of carbon−carbon bonds in organic synthesis. Grignard reagents are typically prepared via reactions between organic halides and magnesium metal in a solvent. However, this method usually requires the use of dry organic solvents, long reaction times, strict control of the reaction temperature, and inert-gas-line techniques. Despite the utility of Grignard reagents, these requirements still represent major drawbacks from both an environmental and an economic perspective, and often cause reproducibility problems. Here, we report the general mechanochemical synthesis of magnesium-based carbon nucleophiles (Grignard reagents in paste form) in air using a ball milling technique. These nucleophiles can be used directly for one-pot nucleophilic addition reactions with various electrophiles and nickel-catalyzed cross-coupling reactions under solvent-free conditions.
• Introduction of a Luminophore into Generic Polymers via Mechanoradical Coupling with a Prefluorescent Reagent (Angew. Chem. 29/2021)
  Koji Kubota; Naoki Toyoshima; Daiyo Miura; Julong Jiang; Satoshi Maeda; Mingoo Jin; Hajime Ito
  Angewandte Chemie, 133, 29, 15793, 15793, Wiley, 2021年07月12日, ［査読有り］
  英語, 研究論文（学術雑誌）
• Introduction of a Luminophore into Generic Polymers via Mechanoradical Coupling with a Prefluorescent Reagent
  Koji Kubota; Naoki Toyoshima; Daiyo Miura; Julong Jiang; Satoshi Maeda; Mingoo Jin; Hajime Ito
  Angewandte Chemie International Edition, 60, 29, 16003, 16008, 2021年07月12日, ［査読有り］
  英語, 研究論文（学術雑誌）
• N-Hydroxybenzimidazole as a structurally modifiable platform forN-oxyl radicals for direct C-H functionalization reactions
  Tomomi Yoshii; Saori Tsuzuki; Shunya Sakurai; Ryu Sakamoto; Julong Jiang; Miho Hatanaka; Akira Matsumoto; Keiji Maruoka
  CHEMICAL SCIENCE, 11, 22, 5772, 5778, 2020年06月, ［査読有り］
  英語, 研究論文（学術雑誌）
• Mechanistic Study on Decarbonylative Phosphorylation of Aryl Amides by Nickel Catalysis
  Yuantai Xu; Bing Wang; Julong Jiang; Haizhu Yu; Yao Fu
  JOURNAL OF ORGANIC CHEMISTRY, 84, 15, 9474, 9479, 2019年08月, ［査読有り］
  英語, 研究論文（学術雑誌）
• A remarkably strained cyclopyrenylene trimer that undergoes metal-free direct oxygen insertion into the biaryl C-C sigma-bond
  Ryo Kurosaki; Hironobu Hayashi; Mitsuharu Suzuki; Julong Jiang; Miho Hatanaka; Naoki Aratani; Hiroko Yamada
  CHEMICAL SCIENCE, 10, 28, 6785, 6790, 2019年07月, ［査読有り］
  英語, 研究論文（学術雑誌）
• Mechanistic insights into the ruthenium-catalyzed site-selective oxidation of alcohols
  Bing Wang; Julong Jiang; Haizhu Yu; Yao Fu
  ORGANIC CHEMISTRY FRONTIERS, 5, 16, 2473, 2478, 2018年08月, ［査読有り］
  英語, 研究論文（学術雑誌）
• Theoretical Investigation on Ni-Catalyzed C(sp(3))-F Activation and Ring Contraction of Tetrahydropyrans: Exploration of an S(N)2 Pathway
  Zheyuan Xu; Yinuo Yang; Julong Jiang; Yao Fu
  ORGANOMETALLICS, 37, 7, 1114, 1122, 2018年04月, ［査読有り］
  英語, 研究論文（学術雑誌）
• Enhanced Reactivity by Torsional Strain of Cyclic Diaryliodonium in Cu-Catalyzed Enantioselective Ring-Opening Reaction
  Kun Zhao; Longhui Duan; Shibo Xu; Julong Jiang; Yao Fu; Zhenhua Gu
  CHEM, 4, 3, 599, 612, 2018年03月, ［査読有り］
  英語, 研究論文（学術雑誌）
• Visible Light Accelerated Vinyl C-H Arylation in Pd-Catalysis: Application in the Synthesis of ortho Tetra-substituted Vinylarene Atropisomers
  Jia Feng; Bin Li; Julong Jiang; Mingkai Zhang; Wenbai Ouyang; Chunyu Li; Yao Fu; Zhenhua Gu
  CHINESE JOURNAL OF CHEMISTRY, 36, 1, 11, 14, 2018年01月, ［査読有り］
  英語, 研究論文（学術雑誌）
• Palladium/Norbornene-Catalyzed ortho Aliphatic Acylation with Mixed Anhydride: Selectivity and Reactivity
  Shibo Xu; Julong Jiang; Linlin Ding; Yao Fu; Zhenhua Gu
  ORGANIC LETTERS, 20, 2, 325, 328, 2018年01月, ［査読有り］
  英語, 研究論文（学術雑誌）
• Mechanism and Origin of the Stereoselectivity in the Palladium-Catalyzed trans Hydroboration of Internal 1,3-Enynes with an Azaborine-Based Phosphine Ligand
  Yinuo Yang; Julong Jiang; Haizhu Yu; Jing Shi
  CHEMISTRY-A EUROPEAN JOURNAL, 24, 1, 178, 186, 2018年01月, ［査読有り］
  英語, 研究論文（学術雑誌）
• Mechanistic Study on Nickel-Catalyzed Silylation of Aryl Methyl Ethers
  Bing Wang; Qi Zhang; Julong Jiang; Haizhu Yu; Yao Fu
  CHEMISTRY-A EUROPEAN JOURNAL, 23, 68, 17249, 17256, 2017年12月, ［査読有り］
  英語, 研究論文（学術雑誌）
• Theoretical Investigation on Nickel-Catalyzed Hydrocarboxylation of Alkynes Employing Formic Acid
  Julong Jiang; Mingchen Fu; Cui Li; Rui Shang; Yao Fu
  ORGANOMETALLICS, 36, 15, 2818, 2825, 2017年08月, ［査読有り］
  英語, 研究論文（学術雑誌）
• Theoretical Investigation on the ClBcat-Promoted Synthesis of Heterocyclic Boronic Esters
  Julong Jiang; Zhenqi Zhang; Yao Fu
  ASIAN JOURNAL OF ORGANIC CHEMISTRY, 6, 3, 282, 289, 2017年03月, ［査読有り］
  英語, 研究論文（学術雑誌）
• Mechanism of Metal-Free C-H Activation of Branched Aldehydes and Acylation of Alkenes Using Hypervalent Iodine Compound: A Theoretical Study
  Julong Jiang; Romain Ramozzi; Shin Moteki; Asuka Usui; Keiji Maruoka; Keiji Morokuma
  JOURNAL OF ORGANIC CHEMISTRY, 80, 18, 9264, 9271, 2015年09月, ［査読有り］
  英語, 研究論文（学術雑誌）
• Rh-III-Catalyzed C(sp(3))-H Bond Activation by an External Base Metalation/Deprotonation Mechanism: A Theoretical Study
  Julong Jiang; Romain Ramozzi; Keiji Morokuma
  CHEMISTRY-A EUROPEAN JOURNAL, 21, 31, 11158, 11164, 2015年07月, ［査読有り］
  英語, 研究論文（学術雑誌）
• Mechanism and Stereoselectivity of Directed C(sp(3))-H Activation and Arylation Catalyzed by Pd(II) with Pyridine Ligand and Trifluoroacetate: A Computational Study
  Julong Jiang; Jin-Quan Yu; Keiji Morokuma
  ACS CATALYSIS, 5, 6, 3648, 3661, 2015年06月, ［査読有り］
  英語, 研究論文（学術雑誌）
• A Mechanistic Study of the Lewis Base-Directed Cycloaddition of 2-Pyrones and Alkynylboranes
  Damien F. P. Crepin; Joseph P. A. Harrity; Julong Jiang; Anthony J. H. M. Meijer; Anne-Chloe M. A. Nassoy; Piotr Raubo
  JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 136, 24, 8642, 8653, 2014年06月, ［査読有り］
  英語, 研究論文（学術雑誌）
• Studies on the stereochemical assignment of 3-acylidene 2-oxindoles
  Steven J. Edeson; Julong Jiang; Stephen Swanson; Panayiotis A. Procopiou; Harry Adams; Anthony J. H. M. Meijer; Joseph P. A. Harrity
  ORGANIC & BIOMOLECULAR CHEMISTRY, 12, 20, 3201, 3210, 2014年, ［査読有り］
  英語, 研究論文（学術雑誌）