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1

Mlinac-Jerković, Kristina, Vladimir Damjanović, Svjetlana Kalanj-Bognar, and Jasna Lovrić. "Marking a Century of the Department of Chemistry and Biochemistry at School of Medicine in Zagreb." Croatica chemica acta 92, no. 3 (2019): 435–42. http://dx.doi.org/10.5562/cca3554.

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In 2018 the Department of Chemistry and Biochemistry at Zagreb School of Medicine celebrated 100 years since it was established by professor Fran Bubanović. This essay is focused on his successors, outstanding teachers and scientists, professors Tomislav Pinter and Mihovil Proštenik, members of Yugoslavian (today Croatian) Academy of Sciences and Arts. Tomislav Pinter was a prominent physical chemist who had an original approach and gave novel interpretation of van der Waals and Wohl’s equations. He also served as the president of Croatian Chemical Society. Neurobiochemist Mihovil Proštenik started as an organic chemist at “Prelog’s Zagreb School of Organic Chemistry”. He collaborated with two Croatian Nobel prize winners in chemistry: his PhD thesis supervisor Vladimir Prelog and Lavoslav Ružička. He was the founder of “Zagreb School of Lipidology”, discovered a new sphingoid base C20-sphingosine, and had a major role in the establishment of Ruđer Bošković Institute. Herein we honor their contributions to Croatian science and beyond, and share so far unpublished valuable material from the Department archive.
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Spichenkova, N. E., and V. E. Vaskovsky. "Bioorganic chemistry: Institutes, journals, publications, a short scientific metric analysis on the 50th anniversary of the Institute of Natural Compound Chemistry, Institute of Bioorganic Chemistry." Russian Journal of Bioorganic Chemistry 35, no. 2 (March 2009): 258–67. http://dx.doi.org/10.1134/s1068162009020162.

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Buchanan, J. Grant. "Sir James Baddiley. 15 May 1918 — 19 November 2008." Biographical Memoirs of Fellows of the Royal Society 56 (January 2010): 3–23. http://dx.doi.org/10.1098/rsbm.2010.0010.

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James Baddiley was a biochemist who used the methods and insight of the organic chemist to answer important questions in biology, notably coenzyme structure and the structure and function of bacterial cell walls. A graduate of Manchester University, he moved to Cambridge in 1944 with A. R. Todd, where he synthesized adenosine triphosphate, the nucleotide concerned with essential energy transformations in all forms of life. As an independent researcher at the Lister Institute in London he elucidated the structure of coenzyme A and other coenzymes. He was appointed Professor of Organic Chemistry in Newcastle, where the exploration of the structures of two cytidine nucleotides led to the discovery of the teichoic acids, major components of the cell walls and membranes of Gram-positive bacteria. These discoveries were extended to cover the structures, biosynthesis, function and immunology of the teichoic acids. Baddiley became Professor of Chemical Microbiology in 1977. Moving to Cambridge after his retirement, he was able to continue his researches in the Department of Biochemistry. He was elected a Fellow of Pembroke College and as an elder statesman undertook extensive committee work, often as chairman, both in Cambridge University and nationally. He was knighted in 1977.
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Zhang, Youshang. "Insulin research in China and the U.K." Biochemical Society Transactions 39, no. 5 (September 21, 2011): 1323–26. http://dx.doi.org/10.1042/bst0391323.

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Insulin has been extensively studied since it was discovered by Banting and Best in 1921. Early in 1934, Dorothy Crowfoot and John Desmond Bernal obtained the first X-ray diffraction photograph of an enzyme protein: pepsin. In 1935, they took another photograph of a protein hormone: insulin. The chemical structure of protein was unknown until the amino acid sequence of bovine insulin was solved by Fred Sanger and colleagues in 1955. In 1958, the chemical synthesis of bovine insulin started in China through a nationwide collaboration of three institutions: the Institute of Biochemistry in Shanghai, the Institute of Organic Chemistry in Shanghai and Beijing University. The total synthesis of bovine insulin in crystalline form was accomplished in 1965. The success of the synthesis of the first protein in vitro greatly encouraged young researchers in China. Not long afterwards, the project of structural analysis of insulin crystal was carried out in China through the collaboration of the Institute of Biophysics, the Institute of Physics and Beijing University, and succeeded in 1971. In Dorothy Hodgkin's laboratory in Oxford, X-ray diffraction studies of insulin crystals were resumed after about 30 years, and the structure of rhombohedral insulin crystal was solved in 1969. Through insulin research, the Institute of Biophysics in Beijing and the Institute of Biochemistry in Shanghai established scientific collaboration and personal friendship with Dorothy Hodgkin's laboratory in Oxford, and later Guy Dodson's laboratory in York and Tom Blundell's laboratory in London. In 1975, Dorothy Hodgkin wrote a short note, ‘Chinese work on insulin’ in Nature, anticipating closer scientific exchange between the East and the West. In 1982, a bilateral meeting between the Biochemical Societies in the U.K. and China was held in Oxford. Now, the second bilateral meeting held in Shanghai will further promote the collaboration between our two countries.
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Kawaguchi, Kichitaro, and Tatsuya Yamagata. "Drs. Sadako and Yasuo Inoue Move to the Institute of Biological Chemistry, Academia Sinica, Taiwan, R. O. C." Trends in Glycoscience and Glycotechnology 8, no. 40 (1996): 143–46. http://dx.doi.org/10.4052/tigg.8.143.

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Wilson, Brice A. P., Christopher C. Thornburg, Curtis J. Henrich, Tanja Grkovic, and Barry R. O'Keefe. "Creating and screening natural product libraries." Natural Product Reports 37, no. 7 (2020): 893–918. http://dx.doi.org/10.1039/c9np00068b.

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7

Wu, Yanqi, Yuehua Wan, and Fengzhi Zhang. "Characteristics and Trends of C-H Activation Research: A Review of Literature." Current Organic Synthesis 15, no. 6 (August 29, 2018): 781–92. http://dx.doi.org/10.2174/1570179415666180426115417.

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Background: C-H activation has attracted great interests over the past two decades, which resulted in an explosive growth in both quality and quantity of published papers related to this topic. Objective: In this review, a bibliometric analysis was performed to evaluate the publications in this field from 1996 to 2015 based on the Science Citation Index (SCI) Expanded database. This work presented a detailed overview of C-H activation from aspects of types of articles, citations, h-indices, languages, years, journals, institutions, countries and author keywords. Conclusion: The results showed that the USA took the leading position in this research field, followed by P. R. China and German. Chinese Academy of Science had the most publications and the highest h-index, Scripps Research Institute won the first place as far as the highest average citation per paper is concerned. Organometallics, Angewandte Chemie International Edition and Journal of the American Chemical Society were the most productive journals in this field, and Chemistry was the most frequently used subject category. Keywords analysis indicated that most research focused on the Palladium, Rhodium and Copper catalyzed cross-coupling synthetic method development for the heterocycle synthesis. The research about exploring the asymmetric C-H functionalization, mechanism investigation and solving the regioselectivity issue is the development trend in this area.
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Tressaud, Alain. "The laureate of the International Moissan Prize 2009 is Herbert W. Roesky, Professor of Chemistry at the Institute for Inorganic Chemistry, Gottingen University, Germany." Journal of Fluorine Chemistry 131, no. 3 (March 2010): 295. http://dx.doi.org/10.1016/j.jfluchem.2009.11.016.

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Conboy, Darren, and Fawaz Aldabbagh. "6-Imino-1,2,3,4,8,9,10,11-octahydropyrido[1,2-a]pyrido[1′,2′:1,2]imidazo[4,5-f]benzimidazole-13-one: Synthesis and Cytotoxicity Evaluation." Molbank 2020, no. 1 (March 5, 2020): M1118. http://dx.doi.org/10.3390/m1118.

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The first report of an iminoquinone of imidazo[4,5-f]benzimidazole is described. The 2D-NOESY spectrum of 1,2,3,4,8,9,10,11-octahydropyrido[1,2-a]pyrido[1’,2’:1,2]imidazo[4,5-f]benzimidazol-6-amine was used to confirm the location of the imine moiety at the C-6 position of the title compound. Cytotoxicity data from the National Cancer Institute are included.
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10

Djoussé, Luc, Richard H. Myers, Hilary Coon, Donna K. Arnett, Michael A. Province, and R. Curtis Ellison. "Smoking influences the association between apolipoprotein E and lipids: The national heart, lung, and blood institute family heart study." Lipids 35, no. 8 (August 2000): 827–31. http://dx.doi.org/10.1007/s11745-000-0591-1.

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11

Witczak, Zbigniew J. "C-Glycoside Synthesis. By Maarten H. D. Postema, (Scripps Research Institute, La Jolla, California), CRC Press Inc. Boca Raton. 1995, 379pp. $ 99.50 in USA/Outside U.S. $119.00. ISBN 0-8413-9150-4." Journal of Carbohydrate Chemistry 15, no. 1 (January 1996): 123–24. http://dx.doi.org/10.1080/07328309608005432.

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12

Umemoto, Teruo, David O’Hagan, and Joseph S. Thrasher. "Professor Norio Shibata, Nagoya Institute of Technology – Recipient of the 2019 American Chemical Society Award for Creative Work in Fluorine Chemistry." Journal of Fluorine Chemistry 234 (June 2020): 109515. http://dx.doi.org/10.1016/j.jfluchem.2020.109515.

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13

Uluçam, Gühergül, and Murat Turkyilmaz. "Synthesis, Structural Analysis, and Biological Activities of Some Imidazolium Salts." Bioinorganic Chemistry and Applications 2018 (2018): 1–12. http://dx.doi.org/10.1155/2018/1439810.

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Four newly synthesized imidazolium salts were characterized by nuclear magnetic resonance, vibrational spectra, and mass spectra. Then, the density functional theory calculations were performed to obtain the molecular configurations on which the theoretical nuclear magnetic resonance and infrared spectra were consequently obtained. The comparison of calculated spectra with the experimental spectra for each molecule leads to the conclusion that the theoretical results can be assumed to be a good approach to their molecular configurations. The in vitro biological activities of the salts on the selected bacteria and cancer cell lines were determined by using the broth dilution method according to Clinical and Laboratory Standards Institute guidelines. The 1,3-bis(2-hydroxyethyl) imidazolidinium bromide and 3-(2-ethoxy-2-oxoethly)-1-(3-aminopropyl)-1H-imidazol-3-ium bromide showed efficiency on Bacillus cereus ATCC 11778. The 3-bis(2-carboxyethyl)-4-methyl-1-H-imidazol-3-ium bromide was effective on HeLa while a similar effect was observed on Hep G2 with 3-(2-carboxyethyl)-1-(3-aminopropyl)-1H-imidazol-3-ium bromide.
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Kahn, Bruce E. "Organic Chemistry in Photography By Shinsaku Fujita (Kyoto Institute of Technology). Springer-Verlag: Berlin, Heidelberg, New York. 2004. xx + 588 pp. $249.00. ISBN 3-540-20988-3." Journal of the American Chemical Society 127, no. 6 (February 2005): 2014–15. http://dx.doi.org/10.1021/ja040975+.

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15

Tykvart, Jan, Václav Navrátil, Michael Kugler, Pavel Šácha, Jiří Schimer, Anna Hlaváčková, Lukáš Tenora, et al. "Identification of Novel Carbonic Anhydrase IX Inhibitors Using High-Throughput Screening of Pooled Compound Libraries by DNA-Linked Inhibitor Antibody Assay (DIANA)." SLAS DISCOVERY: Advancing the Science of Drug Discovery 25, no. 9 (May 26, 2020): 1026–37. http://dx.doi.org/10.1177/2472555220918836.

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The DNA-linked inhibitor antibody assay (DIANA) has been recently validated for ultrasensitive enzyme detection and for quantitative evaluation of enzyme inhibitor potency. Here we present its adaptation for high-throughput screening of human carbonic anhydrase IX (CAIX), a promising drug and diagnostic target. We tested DIANA’s performance by screening a unique compound collection of 2816 compounds consisting of lead-like small molecules synthesized at the Institute of Organic Chemistry and Biochemistry (IOCB) Prague (“IOCB library”). Additionally, to test the robustness of the assay and its potential for upscaling, we screened a pooled version of the IOCB library. The results from the pooled screening were in agreement with the initial nonpooled screen with no lost hits and no false positives, which shows DIANA’s potential to screen more than 100,000 compounds per day. All DIANA screens showed a high signal-to-noise ratio with a Z′ factor of >0.89. The DIANA screen identified 13 compounds with Ki values equal to or better than 10 µM. All retested hits were active also in an orthogonal enzymatic assay showing zero false positives. However, further biophysical validation of identified hits revealed that the inhibition activity of several hits was caused by a single highly potent CAIX inhibitor, being present as a minor impurity. This finding eventually led us to the identification of three novel CAIX inhibitors from the screen. We confirmed the validity of these compounds by elucidating their mode of binding into the CAIX active site by x-ray crystallography.
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Ansarifard, Elham, Zahra Zareshahrabadi, Najmeh Sarafraz, and Kamiar Zomorodian. "Evaluation of Antimicrobial and Antibiofilm Activities of Copper Oxide Nanoparticles within Soft Denture Liners against Oral Pathogens." Bioinorganic Chemistry and Applications 2021 (June 4, 2021): 1–7. http://dx.doi.org/10.1155/2021/9939275.

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Objectives. Soft denture liners provide a favorable environment for adhesion and colonization of microorganisms. This in vitro study aimed to examine the efficacy of different concentrations of copper oxide nanoparticles (CuO NPs) incorporation into soft denture liner on the biofilm formation of the microbial species. Methods. Field Emission Scanning Electron Microscopy (FESEM) images from NPs were recorded. Antifungal susceptibility testing of CuO NPs against five standard strains of Candida albicans (CBS 10261, 1905, 1912, 1949, 2730), Streptococcus mutans (ATCC35668), Streptococcus sobrinus (ATCC27607), and Streptococcus salivarius (ATCC9222) was performed by the broth microdilution method with the Clinical and Laboratory Standards Institute reference method. The biofilm inhibition percentages of CuO NPs on the soft denture liners were determined by XTT assay. Results. The characterization of CuO NPs by scanning electron microscope (SEM) analyses confirmed the synthesis of NPs with appropriate structure and size with a mean diameter of 18.3 ± 9.1 nm. The CuO NPs successfully inhibited the growth of the tested standard strains of C. albicans and Streptococcus spp. at concentrations ranging from 64 to 128 µg mL−1. Indeed, incorporation of CuO NPs at a concentration of 500 µg mL−1 into the soft denture liners exhibited a significant activity (75%) in inhibition of C. albicans. biofilm formation in a dose-dependent manner. The biofilm formation of C. albicans in the presence of CuO NPs was lower than Streptococcus spp. in comparison with the control group ( p < 0.05 ). Conclusion. Incorporation of CuO NPs significantly decreased the colonization and plaque formation of the oral pathogens, especially C. albicans accumulation. These NPs may be useful as a promising agent for the antimicrobial management of soft denture liner materials.
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France, Stefan. "Handbook of Asymmetric Heterogeneous Catalysis Handbook of Asymmetric Heterogeneous Catalysis . Edited by Kuiling Ding (Shanghai Institute of Organic Chemistry, China) and Yasuhiro Uozumi (Institute for Molecular Science, Okazaki, Japan). WILEY-VCH Verlag GmbH & Co. KGaA: Weinheim. 2008. xviii + 448 pp. $200. ISBN 978-3-527-31913-8 ." Journal of the American Chemical Society 131, no. 30 (August 5, 2009): 10791–92. http://dx.doi.org/10.1021/ja9042388.

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Katritzky, Alan, and Eric Scriven. "Organic Azides: Syntheses and Applications Organic Azides: Syntheses and Applications . By Stefan Bräse (Karlsruhe Institute of Technology, Germany) and Klaus Banert (Chemnitz University of Technology, Germany). John Wiley & Sons, Ltd.: Chichester. 2010. xxviii + 508 pp. $200. ISBN 978-0-470-51998-1 ." Journal of the American Chemical Society 132, no. 34 (September 2010): 12156. http://dx.doi.org/10.1021/ja106712z.

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Caputo, F., D. Mehn, J. D. Clogston, M. Rösslein, A. Prina-Mello, S. E. Borgos, S. Gioria, and L. Calzolai. "Asymmetric-flow field-flow fractionation for measuring particle size, drug loading and (in)stability of nanopharmaceuticals. The joint view of European Union Nanomedicine Characterization Laboratory and National Cancer Institute - Nanotechnology Characterization Laboratory." Journal of Chromatography A 1635 (January 2021): 461767. http://dx.doi.org/10.1016/j.chroma.2020.461767.

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Weiss, Paul S. "The Supramolecular Chemistry of Organic-Inorganic Hybrid Materials The Supramolecular Chemistry of Organic-Inorganic Hybrid Materials . Edited by Knut Rurack (BAM Federal Institute for Materials Research and Testing, Berlin, Germany) and Ramón Martínez-Máñez (Polytechnic University of Valencia, Spain). John Wiley & Sons: Hoboken, NJ. 2010. xxxiv + 766 pp. $149.95. ISBN 978-0-470-37621-8 ." Journal of the American Chemical Society 132, no. 31 (August 11, 2010): 10954. http://dx.doi.org/10.1021/ja1059312.

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Schwartz, Jeffrey. "New Aspects of Zirconium Containing Organic Compounds. Topics in Organometallic Chemistry, 10 Edited by Ilan Marek (Technion-Israel Institute of Technology, Haifa). Springer: Berlin, Heidelberg, New York. 2005. x + 176 pp. $149.00. ISBN 3-540-22221-9." Journal of the American Chemical Society 128, no. 21 (May 2006): 7110–11. http://dx.doi.org/10.1021/ja059880d.

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Allan, George F., Amy Hutchins, Xiulin Liu, and Joanna Clancy. "Induction of the progesterone receptor gene in estrogen target cells monitored by branched DNA signal amplification☆ ☆This work originated at the R.W. Johnson Pharmaceutical Research Institute, Raritan, New Jersey, USA." Steroids 66, no. 9 (September 2001): 663–71. http://dx.doi.org/10.1016/s0039-128x(01)00131-3.

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Floreancig, Paul E. "Handbook of Cyclization Reactions, Vols. 1−2 Handbook of Cyclization Reactions, Vols. 1−2 . Edited by Shengming Ma (Shanghai Institute of Organic Chemistry, People’s Republic of China). WILEY-VCH Verlag GmbH & Co, KGaA: Weinheim. 2010. xxi + xxiv + 1265 pp. $430. ISBN: 978-3-527-32088-2 ." Journal of the American Chemical Society 132, no. 19 (May 19, 2010): 6865–66. http://dx.doi.org/10.1021/ja103004f.

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Hammond, Gerald B. "Oxidation and Antioxidants in Organic Chemistry and Biology By Evgeny T. Denisov (Russian Academy of Sciences, Chernogolovka, Russia) and Igor B. Afanas'ev (Vitamin Research Institute, Moscow, Russia). CRC Press (an imprint of Taylor & Francis Group): Boca Raton, FL. 2005. xxxviii + 982 pp. $199.95. ISBN 0-8247-5356-9." Journal of the American Chemical Society 128, no. 13 (April 2006): 4495–96. http://dx.doi.org/10.1021/ja059854f.

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Williams, Vance E. "Functional Organic Materials: Syntheses, Strategies and Applications Edited by Thomas J. J. Müller (Heinrich-Heine-Universität Düsseldorf, Germany) and Uwe H. F. Bunz (Georgia Institute of Technology, Atlanta, GA, USA). Wiley-VCH Verlag GmbH & Co. KGaA: Weinheim. 2007. xx + 592 pp. $335. ISBN 978-3-527-31302-0." Journal of the American Chemical Society 129, no. 46 (November 2007): 14524–25. http://dx.doi.org/10.1021/ja076982q.

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Siegel, Jay S., and Heinz Heimgartner. "Institute of Organic Chemistry: 1983–2008." CHIMIA International Journal for Chemistry 62, no. 3 (March 26, 2008): 114–21. http://dx.doi.org/10.2533/chimia.2008.114.

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Burgess, Kevin. "Chiral Ferrocenes in Asymmetric Catalysis: Synthesis and Applications Chiral Ferrocenes in Asymmetric Catalysis: Synthesis and Applications . Edited by Li-Xin Dai and Xue-Long Hou (both at Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, People’s Republic of China). WILEY-VCH GmbH & Co. KGaA: Weinheim. 2010. xviii + 414 pp. $215.00. ISBN 978-3-527-32280-0 ." Journal of the American Chemical Society 132, no. 29 (July 28, 2010): 10206. http://dx.doi.org/10.1021/ja105679w.

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Bunz, Uwe H. F. "Organic Light-Emitting Devices Edited by Klaus Müllen (Max-Planck-Institut für Polymerforschung) and Ullrich Scherf (Bergische Universität Wuppertal): Wiley-VCH Verlag GmbH & Co. KGaA: Weinheim. 2006. xviii + 410 pp. $170.00. ISBN 3-527-31218-8." Journal of the American Chemical Society 128, no. 20 (May 2006): 6761. http://dx.doi.org/10.1021/ja069724m.

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Kiang, Judy, Lai-Xi Wang, Mei Tang, Shousun C. Szu, and Yuan C. Lee. "Simultaneous determination of glucosamine and glucosamine 4-phosphate in Lipid A with high-performance anion-exchange chromatography (HPAEC)1This work was carried out while YCL was a Scholar-in-Residence (1995–1998) at the Fogarty International Center for Advanced Study in the Health Sciences, National Institutes of Health, Bethesda, Maryland, USA. The authors are indebted to Dr. H.C. Chen (NIH, NICHD) for initiation of this work.1." Carbohydrate Research 312, no. 1-2 (November 1998): 73–76. http://dx.doi.org/10.1016/s0008-6215(98)00226-2.

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Gryko, Daniel T. "Institute of Organic Chemistry, Polish Academy of Sciences." European Journal of Organic Chemistry 2018, no. 47 (December 14, 2018): 6599. http://dx.doi.org/10.1002/ejoc.201801774.

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Kalvinsh, I. "The Latvian Institute of Organic Synthesis-Quo Vadis?" Chemistry of Heterocyclic Compounds 43, no. 2 (February 2007): 123–26. http://dx.doi.org/10.1007/s10593-007-0022-0.

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Wintner, Claude E. "Recollecting the Institute of Organic Chemistry, ETH Zürich, 1972–1990." CHIMIA International Journal for Chemistry 60, no. 3 (March 28, 2006): 142–48. http://dx.doi.org/10.2533/000942906777675029.

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Shermolovich, Yurii, and Tatyana Vasilievа. "INSTITUTE OF ORGANIC CHEMISTRY OF NAS OF UKRAINE - 80 YEARS." Ukrainian Chemistry Journal 85, no. 12 (December 16, 2019): 117–27. http://dx.doi.org/10.33609/0041-6045.85.11.2019.117-127.

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The article is devoted to the history and present of the Institute of Organic Chemistry of NAS of Ukraine. By Boris Paton's definition, the Institute of Organic Chemistry belongs to the memorial institutions of the National Academy of Sciences of Ukraine. On May 23, 1939, the Presidium of the USSR Academy of Sciences, according to resolution of the Council of People's Commissars of the USSR (May 8, 1939) decided to set up the Institute of Organic Chemistry and Technology of the USSR Academy of Sciences and the Institute of Organic Chemistry of the Ukrainian Academy of Sciences. There were four scientific departments in the Institute, headed by academicians of the Academy of Sciences of the Ukrainian SSR: General Organic Synthesis - V.P. Jaworski, fuel - M.I. Kuznetsov, macromolecular compounds - I.K. Matsurevich, fibrous substances and dyes - V.G. Shaposhnikov at the time of its foundation. V. P. Jaworski, the academician of the Academy of Sciences of the Ukrainian SSR, was the first Director of the Institute. Since the institute's existence, such outstanding scientists have worked in the institution as: Andrei Kiprianov (founder of the color theory of organic dyes, phenomenon of interaction of chromophores "Phenomenon AI Kiprianov", VM Zubarovsky, OI Tolmachov, Yu.L. Slominsky, OO Ishchenko, KD Sych, IK Ushenko, FA (development of preparative chemistry of thiazole, benzothiazole, benzimidazole and a number of heterocycles), E.O. Shilov (formation of p-complexes of molecules of unsaturated compounds with electrophilic reagents, substantiation of mechanisms of biochemical processes), OA Yasnikov (theory of radical transformations in reactions modeling nicotinamide coenzymes, open catalytic properties of cytochrome production technology for phospho-rylated starch), OV Kirsanov (reaction of amino compounds with phosphorus pentachloride and reaction of oxidative imination of compounds of trivalent phosphorus with dichloramines), A.F. Plate, IL Knunanciec, M.I. Kabachnik, L.M. Markovsky (Chemistry of Sulfur Organic Com-pounds) and VP Kuchar (Works on Chemistry of Phosphorus Organic Compounds), Yu. Gololobov (Chemistry of Organo-Organic Compounds), A.D. Sinitsa (Methods of Synthesis and Investigation of the Properties of Imino-Phosphonates), OI Kolodyazhny (Chemistry of Phosphorus Illides), L.M. Yagupolsky (Yagupolsky principle, Buchwald – Hartwig – Yagupolsky reaction), M.O. Lozynsky, S.V. Komisarenko (chemistry of physiologically active heterocyclic compounds), V.I. Kalchenko (molecular design, synthesis and study of supramolecular interactions of macrocyclic compounds - crowneters, calixarenes, thiacalixarenes and calixresorbins). The Institute's developments have great innovation potential today. The Institute's staff published 8,000 scientific articles, 90 monographs and obtained 1550 copyright certificates and patents. The Institute has trained 350 candidates and 65 doctors of science during its work.
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Raker, Jeffrey, Thomas Holme, and Kristen Murphy. "The ACS Exams Institute Undergraduate Chemistry Anchoring Concepts Content Map II: Organic Chemistry." Journal of Chemical Education 90, no. 11 (September 13, 2013): 1443–45. http://dx.doi.org/10.1021/ed400175w.

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Witkop, Bernhard. "A Chemist in a Biomedical Institute." HETEROCYCLES 49, no. 1 (1998): 5. http://dx.doi.org/10.3987/1998-01-0005.

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Lukevics, E. "The fortieth anniversary of the Latvian Institute of Organic Synthesis." Chemistry of Heterocyclic Compounds 33, no. 2 (February 1997): 127–29. http://dx.doi.org/10.1007/bf02256752.

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Heller, Stephen R. "Similarity in organic chemistry: A summary of the Beilstein Institute Conference." Journal of Chemical Information and Modeling 32, no. 6 (November 1, 1992): 578–79. http://dx.doi.org/10.1021/ci00010a001.

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Minkin, Vladimir I. "Institute of Physical and Organic Chemistry at the Rostov State University." Russian Chemical Reviews 71, no. 11 (November 30, 2002): 867–68. http://dx.doi.org/10.1070/rc2002v071n11abeh000760.

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Ding, Kuiling, and Shengming Ma. "Virtual Issue on Catalysis at the Shanghai Institute of Organic Chemistry." ACS Catalysis 3, no. 7 (June 26, 2013): 1633. http://dx.doi.org/10.1021/cs4004326.

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Jiang, Xuefeng. "Cluster Preface: Perspectives on Organoheteroatom and Organometallic Chemistry." Synlett 32, no. 13 (July 28, 2021): 1260–61. http://dx.doi.org/10.1055/s-0040-1720387.

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Xuefeng Jiang is a professor at East China Normal University. He received his B.S. degree in 2003 from Northwest University (China). He then joined Professor Shengming Ma’s research group at the Shanghai Institute of Organic Chemistry (SIOC), Chinese Academy of Sciences, where he received his Ph.D. degree in 2008. From 2008 to 2011, Xuefeng worked as a postdoctoral researcher on the total synthesis of natural products in the research group of Professor K. C. Nicolaou at The Scripps Research Institute (TSRI). His independent research interests have focused on green organosulfur chemistry and methodology-­oriented total synthesis.
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Wood, E. J. "Organic chemistry." Biochemical Education 23, no. 1 (January 1995): 44. http://dx.doi.org/10.1016/0307-4412(95)90196-5.

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42

Pashinnik, Valery E. "Advances in the chemistry of organylfluorosulfuranes at the Institute of Organic Chemistry, Kiev, Ukraine." Journal of Fluorine Chemistry 117, no. 2 (October 2002): 85–98. http://dx.doi.org/10.1016/s0022-1139(02)00184-7.

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43

BANCIU, M. D. "ChemInform Abstract: Dibenzocycloalkane Chemistry in the Organic Chemistry Laboratory of the Polytechnic Institute Bucharest." ChemInform 26, no. 9 (August 18, 2010): no. http://dx.doi.org/10.1002/chin.199509252.

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Bulski, Wojciech, Barbara Gwiazdowska, and Jerzy Tołwiński. "Radium Institute in Warsaw – the ancestor of the Institute of Oncology: The radium era." Analytical and Bioanalytical Chemistry 400, no. 6 (April 13, 2011): 1587–92. http://dx.doi.org/10.1007/s00216-011-4900-z.

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Olsufyeva, E. N., and M. N. Preobrazhenskaya. "Antibiotics produced at the G. F. Gauze Scientific-Research Institute of New Antibiotics, Russian Academy of Medical Sciences (marking the Fiftieth Anniversary of the Institute). (Review)." Chemistry of Heterocyclic Compounds 40, no. 11 (November 2004): 1381–95. http://dx.doi.org/10.1007/s10593-005-0049-z.

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Zhu, Chen, and Xin-Yuan Liu. "Cluster Preface: Radicals – by Young Chinese Organic Chemists." Synlett 32, no. 04 (February 16, 2021): 354–55. http://dx.doi.org/10.1055/s-0040-1706715.

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(left) received his B.S. degree from Xiamen University in 2003 under the supervision of Prof. Pei-Qiang Huang, and his Ph.D. degree from the Shanghai Institute of Organic Chemistry in 2008 under the supervision of Prof. Guo-Qiang Lin. After postdoctoral research at ­Gakushuin University, Japan with Prof. Takahiko Akiyama, he moved to the University of Texas Southwestern Medical Center, working as a postdoctoral fellow with Prof. John R. Falck and Prof. Chuo Chen. He was appointed as a professor at Soochow University, China in December 2013. He is currently the Head of the Organic Chemistry Department at Soochow University. His current research interests include radical-mediated transformations, in particular radical ­rearrangements, and their applications in the construction of natural products and biologically active compounds. Xin-Yuan Liu (right) obtained his B.S. degree from Anhui Normal University (AHNU) in 2001. He continued his research studies at both the Shanghai Institute of Organic Chemistry (SIOC), CAS and AHNU under the joint supervision of Prof. Dr. Shizheng Zhu and Prof. Dr. Shaowu Wang, obtaining his master’s degree in 2004. After a one-year stint in Prof. Gang Zhao’s laboratory at SIOC, he joined Prof. Dr. Chi-Ming Che’s group at The University of Hong Kong (HKU) and earned his Ph.D. degree in 2010. He subsequently undertook postdoctoral studies in Prof. Che’s group at HKU and in Prof. Carlos F. Barbas III’s group at The Scripps Research Institute. At the end of 2012, he began his independent academic career at the Southern University of Science and Technology (SUSTech) and was promoted to a tenured Full Professor of SUSTech in 2018. His research interests are directed towards the design of novel chiral anionic ligands to solve radical-involved asymmetric reactions.
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Hancock, William S. "National Cancer Institute Shows The Way." Journal of Proteome Research 2, no. 3 (June 2003): 233. http://dx.doi.org/10.1021/pr030790m.

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Belen'kii, L. I. "N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences: 70 Years." Chemistry of Heterocyclic Compounds 40, no. 3 (March 2004): 387–91. http://dx.doi.org/10.1023/b:cohc.0000028637.84165.dc.

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Egorov, Mikhail P. "N D Zelinsky Institute of Organic Chemistry of the Russian Academy of Sciences." Russian Chemical Reviews 78, no. 8 (August 31, 2009): 679–81. http://dx.doi.org/10.1070/rc2009v078n08abeh004085.

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Muldakhmetov, Z. М. "Institute of Organic Synthesis and Coal Chemistry: the present state and development prospects." Bulletin of the Karaganda University. "Chemistry" series 94, no. 2 (June 28, 2019): 88–104. http://dx.doi.org/10.31489/2019ch2/88-104.

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