Dr. Ji-Wei Ren | Organic Chemistry | Best Researcher Award

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Dr. Ji-Wei Ren | Organic Chemistry | Best Researcher Award

Dr. Ji-Wei Ren, Organic Chemistry, Taishan University , China 

Dr. Ji-Wei Ren is a Lecturer in the College of Chemistry and Chemical Engineering at Taishan University, China. He earned his Ph.D. in Chemical Engineering and Technology from Central South University, where he developed expertise in visible light catalysis, organo catalysis, and green synthesis. Dr. Ren has previously served as a Research Associate at Ningbo University’s Institute of Drug Discovery Technology, engaging in interdisciplinary research on biomimetic reducing agents and chiral resolution. With a strong foundation in heterocyclic construction and peptide synthesis, his work integrates sustainable and biomimetic chemistry with modern synthetic methodologies. Dr. Ren has published multiple high-impact research articles in leading journals such as Org. Lett., J. Org. Chem., and Org. Chem. Front.. His research is characterized by innovation, precision, and relevance to both pharmaceutical and materials chemistry. He actively contributes to academic platforms like ORCID and collaborates with renowned scientists across China.

Professional Profile :         

Orcid

Scopus 

Summary of Suitability for Award:

Dr. Ji-Wei Ren exemplifies the qualities of an outstanding researcher through his pioneering work in the field of organic synthesis, particularly in visible light catalysis, organocatalysis, and green chemistry. He has published over 11 peer-reviewed articles in top-tier journals such as Organic Chemistry Frontiers, Journal of Organic Chemistry, Organic Letters, and Chemistry – A European Journal. Several of his works have been highlighted by Synfacts, showcasing their novelty and scientific impact. His innovative contributions include the development of racemization-free synthesis protocols, the application of biomimetic reducing agents, and the design of sustainable methodologies for heterocycle and peptide construction. He brings a fresh perspective to traditional synthetic methods by incorporating visible light and bio-inspired techniques, addressing both the efficiency and environmental responsibility in chemical synthesis. Dr. Ji-Wei Ren is highly suitable for the “Best Researcher Award”. His significant scientific output, innovation in research, recognition by the international community, and dedication to sustainable chemistry clearly distinguish him as a leading researcher in his field. His commitment to impactful and environmentally conscious science makes him not only an excellent candidate but also a role model for emerging researchers. This award would be a deserving recognition of his ongoing contributions to the scientific world.

🎓Education:

Dr. Ji-Wei Ren completed both his undergraduate and doctoral studies at Central South University. He earned his Bachelor of Engineering in Pharmaceutical Engineering in June 2013, where he gained foundational knowledge in pharmaceutical chemistry, drug design, and synthesis. Subsequently, he pursued a Doctorate in Chemical Engineering and Technology (2013–2019) at the same university. His Ph.D. research focused on innovative synthetic strategies using organo catalysis and visible-light-driven methodologies for the construction of functional molecules, especially in the development of peptide and heterocyclic compounds. Under the mentorship of distinguished faculty, he honed his skills in reaction design, stereoselective synthesis, and catalysis. His academic training also included a deep understanding of biomimetic reactions, green synthesis, and photochemical transformations. This robust educational background laid the groundwork for his interdisciplinary research efforts, enabling him to contribute significantly to the fields of sustainable and asymmetric synthesis.

🏢Work Experience:

Dr. Ji-Wei Ren began his academic career as a Research Associate (2019–2022) at the Institute of Drug Discovery Technology, Ningbo University, where he focused on peptide synthesis and the development of bio-inspired reducing agents. His role involved collaborative projects in pharmaceutical chemistry and catalysis, contributing to the advancement of efficient and eco-friendly synthetic methods. In August 2022, he joined Taishan University as a Lecturer in the College of Chemistry and Chemical Engineering. At Taishan University, Dr. Ren continues his research in visible light catalysis and organocatalytic transformations, guiding students in advanced organic chemistry techniques and experimental methodologies. He has also contributed to curriculum development and interdisciplinary research programs. His teaching and research philosophy is rooted in innovation, sustainability, and student engagement. With over a decade of academic training and research, Dr. Ren combines a strong theoretical foundation with hands-on experience in both industrial and academic labs.

🏅Awards: 

Dr. Ji-Wei Ren has been consistently recognized for his impactful contributions to organic chemistry and green synthesis methodologies. His 2021 publication in Organic Letters was highlighted by Synfacts in 2022 for its innovative racemization-free synthesis approach, underlining the originality and practical importance of his work. Additionally, his earlier work in The Journal of Organic Chemistry (2017) was also spotlighted in Synfacts, reflecting his ongoing excellence in visible light-mediated and organocatalytic transformations. During his doctoral studies at Central South University, he was honored with multiple academic excellence awards for his outstanding research and scholarly dedication. His publications in top-tier journals like Organic Chemistry Frontiers, Organic & Biomolecular Chemistry, and Chemistry – A European Journal have further established him as a rising expert in his field. These recognitions underscore both the scientific value and the practical applicability of his research in modern organic synthesis.

🔬Research Focus:

Dr. Ji-Wei Ren’s research is centered on the development of innovative, environmentally friendly methodologies in organic synthesis. His primary interests lie in visible light catalysis, where he designs photochemical processes to enable mild and selective transformations. He is also deeply involved in chiral resolution and organocatalysis, with a particular emphasis on enantioselective reactions that are crucial for pharmaceutical synthesis. A significant part of his work involves constructing complex heterocyclic compounds, often using biomimetic and green synthesis strategies to reduce environmental impact. Dr. Ren has pioneered the use of L-amino acid esters as biomimetic reducing agents and introduced new deoxygenation and amidation protocols that avoid racemization—critical for peptide and amide bond formation. His interdisciplinary approach blends traditional organic chemistry with sustainability, aiming to create scalable, efficient, and selective processes suitable for industrial application. His contributions significantly enhance both academic understanding and practical implementation in organic synthesis.

Publication Top Notes:

“A visible light-mediated deoxygenation protocol for the synthesis of dipeptides, amides and esters without racemization”​

“L-Amino acid ester as a biomimetic reducing agent for the reduction of unsaturated C=C bonds”

“Umpolung Strategy for the One-Pot Synthesis of Highly Steric Bispirooxindoles via the L-Amino Acid Ester-Promoted In Situ Reduction/Nucleophilic Addition/Cyclization Cascade Reaction”​

“A visible light-induced deoxygenative amidation protocol for the synthesis of dipeptides and amides”​

“An organocatalytic enantioselective ring-reorganization domino sequence of methyleneindolinones with 2-aminomalonates”​

“Straightforward Synthesis of 3-Selenocyanato-Substituted Chromones through Electrophilic Selenocyanation of Enaminones under Grinding Conditions”​

“Organocatalytic, Enantioselective, Polarity-Matched Ring-Reorganization Domino Sequence Based on the 3-Oxindole Scaffold”

“A One‐Pot Ring‐Opening/Ring‐Closure Sequence for the Synthesis of Polycyclic Spirooxindoles”​

“L-Pyroglutamic Sulphonamide as Hydrogen-Bonding Organocatalyst: Enantioselective Diels–Alder Cyclization to Construct Carbazolespirooxindoles”

“Acid-Relayed Organocatalytic exo-Diels-Alder Cycloaddition of Cyclic Enones with 2-Vinyl-1H-indoles”

 

Ms. Apurva Singh | Organic Chemistry | Best Researcher Award

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Ms. Apurva Singh | Organic Chemistry | Best Researcher Award

Ms. Apurva Singh | Organic Chemistry | PhD at Indian institute of technology Roorkee, India

Apurva Singh is an organic chemistry  with a keen interest in technological advancements and artificial intelligence applications in chemistry. With five years of research experience in academic laboratories and two years as a tutor, she specializes in organic synthesis and catalysis. Currently pursuing her Ph.D. at IIT Roorkee under Prof. Naseem Ahmed, she is engaged in process chemistry, exploring new methodologies using homogeneous and heterogeneous catalysis. Apurva has a strong publication record in international journals, reflecting her expertise and dedication to scientific research. She is highly motivated, analytical, and committed to knowledge exchange. Her enthusiasm for teaching, research, and interdisciplinary collaboration makes her a dynamic professional in the field of chemistry.

Professional Profile : 

Orcid

Scopus 

Summary of Suitability for Award:

Apurva Singh is a highly promising researcher in the field of organic synthesis and catalysis, demonstrating a strong commitment to scientific innovation. With five years of research experience at IIT Roorkee, she has contributed significantly to the development of novel catalytic methodologies, particularly in transition-metal catalysis, oxidation reactions, and organo catalysis. Her research has led to multiple publications in high-impact journals, including RSC, Synthesis (Thieme), and Organic & Biomolecular Chemistry, showcasing her ability to conduct impactful studies. Additionally, she has received prestigious poster awards at national and international conferences, underscoring her ability to effectively present and communicate her findings. Given her strong publication record, innovative research contributions, and recognition through awards, Apurva Singh is a highly suitable candidate for the “Best Researcher Award.” Her work in catalysis and organic synthesis, coupled with her dedication to advancing chemical sciences, makes her a deserving nominee for this prestigious recognition.

🎓Education:

Apurva Singh is currently pursuing her Ph.D. in Organic Synthesis and Catalysis at the Indian Institute of Technology (IIT) Roorkee under the mentorship of Prof. Naseem Ahmed. Her research focuses on developing innovative catalytic methodologies for organic transformations, with publications in reputed journals such as RSC and Synthesis (Thieme). Prior to her Ph.D., she completed her Master of Science (M.Sc.) in Chemistry from Chaudhary Charan Singh University (CCSU), Meerut, in 2017, securing a first-class distinction with 76%. During her postgraduate studies, she gained expertise in organic chemistry and reaction mechanisms, further strengthening her foundation in the subject. Additionally, she pursued a Bachelor of Education (B.Ed.) from CCSU, Meerut, from 2018 to 2020, achieving 80%. Her B.Ed. degree equipped her with essential teaching skills, enhancing her ability to mentor and guide students in the academic field. Apurva’s strong academic background demonstrates her dedication to both research and education.

🏢Work Experience:

Apurva Singh has over five years of research experience in organic chemistry, specializing in catalysis, and two years of teaching experience. She is currently a Ph.D. researcher at IIT Roorkee, working on process chemistry, where she investigates novel catalytic methodologies for organic synthesis. Her research involves designing transition-metal complexes for oxidation reactions and developing regio selective synthetic strategies. She has published multiple research articles in internationally recognized journals, highlighting her contributions to the field. Apart from research, she has two years of experience as an academic tutor, mentoring undergraduate and postgraduate students in organic chemistry. She has assisted in research activities, manuscript writing, and conference presentations. Her expertise extends to coding for computational chemistry applications, bridging experimental and theoretical approaches. Apurva’s proactive nature and strong communication skills enable her to collaborate effectively, making significant contributions to both research and academic training.

🏅Awards: 

Apurva Singh has received multiple accolades for her outstanding research contributions. In 2024, she was awarded the Poster Award at the Indian Academy of Sciences Meeting and Lecture Workshop held at IIT Roorkee, recognizing her innovative work in catalysis and organic synthesis. In the same year, she won another Poster Award at the 2nd International Conference on Molecules to Materials at NIT Hamirpur, further establishing her expertise in the field. These awards highlight her ability to present complex scientific findings effectively and her dedication to advancing research. Her work has been widely appreciated for its significance in developing new catalytic methodologies, and she continues to be an active participant in scientific conferences and symposiums. Apurva’s achievements reflect her commitment to excellence in research and academia, positioning her as a promising scientist in the field of organic chemistry.

🔬Research Focus:

Apurva Singh’s research focuses on organic synthesis and catalysis, with a strong emphasis on developing novel transition-metal complexes for oxidation reactions. She explores homogeneous and heterogeneous catalysis to improve reaction efficiency and selectivity, mimicking enzymatic processes for sustainable chemistry. Her work includes the design of μ-chlorido-bridged dimanganese(II) complexes to replicate galactose oxidase enzyme activity, offering applications in oxidation and aldol reactions. She is also engaged in Fenton free radical reactions for regio selective synthesis of complex molecules. Her recent studies on organocatalytic synthesis of bioactive pyrazoline and pyrimidine derivatives contribute to medicinal chemistry by targeting bacterial enzymes like thymidine kinase in Staphylococcus aureus. Apurva is particularly interested in the intersection of chemistry and artificial intelligence, leveraging computational tools to predict reaction mechanisms and optimize catalyst design. Her multidisciplinary approach bridges fundamental chemistry with emerging technologies, driving innovation in organic synthesis and process chemistry.

Publication Top Notes:

1. Nickel(II)-hydrazineylpyridine catalyzed regioselective synthesis of α-benzyl substituted β-hydroxy ketones via a Fenton free radical reaction

Authors: Not provided in the given data

Year: 2025

Journal: Organic & Biomolecular Chemistry

2. Oxidative Cyclization Reactions Catalyzed by Designed Transition-Metal Complexes: A New Strategy for the Synthesis of Flavone, Quinolone, and Benzofuran Derivatives

Authors: Not provided in the given data

Year: 2023

Journal: Synthesis

3. Designed μ-Chlorido-bridged dimanganese(II) complexes to mimic the activity of galactose oxidase enzyme: Application in the dehydrogenative oxidation of alcohol and aldol reaction

Authors: Not provided in the given data

4. Organocatalytic synthesis of novel pyrazoline and pyrimidine derivatives as potent thymidine kinase inhibitors targeting Staphylococcus aureus

Authors: M.I. Issa Alahmdi

Year: 2025

 

 

Dr. Hongjian Qin | Organic Chemistry | Best Researcher Award

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Dr. Hongjian Qin | Organic Chemistry | Best Researcher Award

Dr. Hongjian Qin , Shanghai Institute of Materia Medica, CAS , China

Dr. Hongjian Qin is an accomplished researcher in sustainable and green chemistry, with expertise in drug process development and medicinal administration. He earned his Ph.D. in Organic Chemistry from the Chinese Academy of Sciences, being recognized as an Excellent Graduate in 2024. Dr. Hongjian Qin’s contributions to the field span over three years, emphasizing environmentally friendly pharmaceutical synthesis and active pharmaceutical ingredient (API) development. Currently serving as Research Director at Topharman Company Limited, he continues to advance innovative solutions in drug development. His work includes mentoring students, enhancing resource recovery, and participating in COVID-19 research. With numerous impactful publications, Dr. Hongjian Qin is a dedicated professional committed to promoting sustainability and advancing solutions for global environmental challenges.

Professional Profile:

Scopus 

Summary of Suitability for Award:

Dr. Hongjian Qin is an exemplary candidate for the “Best Researcher Awards,” with a distinguished career in sustainable and green chemistry. His pioneering research in eco-friendly pharmaceutical synthesis has significantly contributed to reducing industrial waste and enhancing process efficiency, aligning with global sustainability objectives. Dr. Hongjian Qin’s innovative work on ligand-free catalysis, large-scale API production, and impurity profiling reflects his expertise in developing practical solutions for complex challenges in organic chemistry and medicinal chemistry. Dr. Hongjian Qin’s research excellence, innovative contributions, and global impact make him a highly deserving candidate for the “Best Researcher Awards.” His work not only addresses critical scientific challenges but also fosters sustainable practices in drug development, making a lasting impact on both academia and industry.

🎓Education:

Dr. Hongjian Qin holds a Ph.D. in Organic Chemistry from the Chinese Academy of Sciences , specializing in process development of drug substances and medicinal administration. His doctoral work was conducted at the Key Laboratory of Plant Resources and Chemistry in Arid Regions, showcasing expertise in sustainable pharmaceutical synthesis. He completed a Master of Engineering in Organic Chemistry from Guangxi University, focusing on the process development of drug substances. Dr. Qin’s academic journey began with a Bachelor of Science in Organic Chemistry from Guangxi University . His educational foundation combines rigorous theoretical knowledge with practical applications, preparing him to address complex challenges in green and sustainable chemistry.

🏢Work Experience:

Dr. Hongjian Qin’s professional journey spans over a decade, focusing on pharmaceutical synthesis and sustainable chemistry. As Research Director at Topharman Company Limited (2024–present), he spearheads innovations in active pharmaceutical ingredients (APIs) and emphasizes good manufacturing practices (GMP). Previously, as a Research Assistant at the Shanghai Institute of Materia Medica (2021–2024), he supported COVID-19 research projects, trained students, and enhanced pharmaceutical waste recovery techniques. At the Xinjiang Engineering Research Centre for Key Technologies and Processes of Ethnomedicine (2015–2021), Dr. Hongjian Qin led projects on sustainable API production and industrial resource recovery. His experiences reflect a blend of academic research and industrial application, driving advancements in pharmaceutical science.

🏅Awards: 

Dr. Hongjian Qin has received numerous accolades for his contributions to sustainable chemistry. He was honored as an Excellent Graduate in 2024 by the University of Chinese Academy of Sciences for his outstanding academic achievements during his Ph.D. studies. His work on sustainable pharmaceutical synthesis earned him recognition at various national and international conferences. Dr. Hongjian Qin has been instrumental in developing innovative processes for drug substances, garnering appreciation from industrial partners. Additionally, his mentorship roles and administrative contributions at research institutions have been commended, underscoring his commitment to advancing science and education.

🔬Research Focus:

Dr. Hongjian Qin’s research focuses on sustainable and green chemistry, particularly in the process development of drug substances. He has worked extensively on optimizing synthesis methods for pharmaceutical intermediates, reducing waste, and improving efficiency in drug manufacturing. His innovative approaches emphasize the use of eco-friendly reagents and catalysts, aligning with global sustainability goals. His recent work includes developing ligand-free copper-catalyzed cyclization methods, novel iron-catalyzed cross-coupling reactions, and efficient large-scale processes for active pharmaceutical ingredients (APIs). Dr. Hongjian Qin is dedicated to advancing environmentally responsible techniques in pharmaceutical synthesis, ensuring both industrial viability and ecological preservation.

Publication Top Notes:

1. Direct Esterification of Amides by the Dimethylsulfate-Mediated Activation of Amide C–N Bonds

Authors: Qin, H.; Han, Z.; Bonku, E.M.; Shen, J.; Aisa, H.A.

Year: 2024

Citations: 0

2. An Alternative Approach to Synthesize Sildenafil via Improved Copper-Catalyzed Cyclization

Authors: Odilov, A.; Gong, X.; Qin, H.; Yang, F.; Shen, J.

Year: 2024

Citations: 0

3. Impurity Study of Tecovirimat (Open Access)

Authors: Bonku, E.M.; Qin, H.; Odilov, A.; Wang, X.; Shen, J.

Year: 2024

Citations: 1

4. Improved and Ligand-Free Copper-Catalyzed Cyclization for an Efficient Synthesis of Benzimidazoles from o-Bromoarylamine and Nitriles (Open Access)

Authors: Bonku, E.M.; Qin, H.; Odilov, A.; Aisa, H.A.; Shen, J.

Year: 2024

Citations: 2

5. Direct Reductive N-Alkylation of Amines with Carboxylic Esters

Authors: Zhang, Y.; Bonku, E.M.; Yang, X.; Shen, J.; Qin, H.

Year: 2024 (In Press)

Citations: 0

6. Iron-Catalyzed Cross-Coupling Reactions of Alkyl Grignard Reagents with Alkenyl Carbonate

Authors: Qin, H.; Yang, X.; Mintah Bonku, E.; Shen, J.; Akber Aisa, H.

Year: 2024 (In Press)

Citations: 0

7. A Review of the Synthetic Strategies Toward the Antiviral Drug Tecovirimat (Review Article)

Authors: Bonku, E.M.; Qin, H.; Odilov, A.; Zhu, F.; Shen, J.

Year: 2024 (In Press)

Citations: 0

8. An Improved Iodine-Catalyzed Aromatization Reaction and Its Application in the Synthesis of a Key Intermediate of Cannabidiol

Authors: Abduahadi, S.; Bonku, E.M.; Qin, H.; Aisa, H.A.; Shen, J.

Year: 2024 (In Press)

Citations: 0

9. Optimized Synthesis of the Key Intermediate of Telmisartan via the Cyclization of 2-Bromoarylamine with n-Butyronitrile

Authors: Qin, H.; Mintah Bonku, E.; Odilov, A.; Zhu, F.; Aisa, H.A.

Year: 2023

Citations: 1

10. Efficient Large-Scale Process for Tecovirimat via Reactive Distillation for the Preparation of Cycloheptatriene

Authors: Bonku, E.M.; Qin, H.; Odilov, A.; Guma, S.D.; Shen, J.

Year: 2023

Citations: 4