Relevant bibliographies by topics / Synthesis and Herbicidal Activity

Contents

  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers
  6. Reports

Academic literature on the topic 'Synthesis and Herbicidal Activity'

Author: Grafiati
Published: 5 June 2025
Last updated: 1 August 2025

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Journal articles on the topic "Synthesis and Herbicidal Activity"

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Bulatov, Anton, Svetlana Savinova, Ksenia Sergeeva, Marina Stepanenko, and Nina Gerasimova. "Synthesis of new herbicides from the class of sulfonylureas." From Chemistry Towards Technology Step-By-Step 6, no. 2 (2025): 120–26. https://doi.org/10.52957/2782-1900-2025-6-2-120-126.

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The authors first synthesised sulfonylurea derivatives incorporating 6 methyluracil and 1,3,4-thiadiazole fragments with 79-81 % yield. The authors conducted field tests of the obtained compounds to determine their herbicidal activity. As a result, the synthesised compounds exhibit a herbicidal activity (53%) close to that of Rubit (61%) and higher than that of Magnum herbicide (41%).
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Wang, Shumin, Na Li, Shibo Han, et al. "Synthesis, Herbicidal Activity, and Molecular Mode of Action Evaluation of Novel Quinazolinone—Phenoxypropionate Hybrids Containing a Diester Moiety." Agronomy 14, no. 9 (2024): 2124. http://dx.doi.org/10.3390/agronomy14092124.

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To develop aryloxyphenoxypropionate herbicides with novel structure and improved activity, a total of twenty-eight novel quinazolinone–phenoxypropionate derivatives containing a diester moiety were designed and synthesized. The herbicidal bioassay results in the greenhouse showed that QPEP-I-4 exhibited excellent herbicidal activity against E. crusgalli, D. sanguinalis, S. alterniflora, E. indica, and P. alopecuroides with inhibition rates >80% at a dosage of 150 g ha−1 and displayed higher crop safety to G. hirsutum, G. max, and A. hypogaea than the commercial herbicide quizalofop-p-ethyl.
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Chen, Ke, Shumin Wang, Shuyue Fu, et al. "Design, Synthesis, and Herbicidal Activity of Novel 5-Acylbarbituric Acid Derivatives Containing a Pyrimidinedione Moiety." Agronomy 15, no. 4 (2025): 777. https://doi.org/10.3390/agronomy15040777.

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In continuation of our efforts to identify novel herbicide lead compounds with enhanced activity, a series of eighteen 5-acylbarbituric acid derivatives containing a pyrimidinedione moiety were designed and synthesized. Their herbicidal activities were subsequently evaluated in the greenhouse. Bioassay results demonstrated that most of the newly synthesized compounds exhibited significant herbicidal efficacy at a dosage of 150 g ha−1, with compounds BA-I-2, BA-II-2, BA-III-2, and BA-III-5 achieving complete inhibition of the tested weeds. Further investigation into the herbicidal spectrum reve
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Wu, Lei, Yu-Cheng Gu, Yong-Hong Li, Sha Zhou, Zhong-Wen Wang, and Zheng-Ming Li. "Synthesis, Herbicidal Activity, Crop Safety and Soil Degradation of Pyrimidine- and Triazine-Substituted Chlorsulfuron Derivatives." Molecules 27, no. 7 (2022): 2362. http://dx.doi.org/10.3390/molecules27072362.

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Chlrosulfuron, a classical sulfonylurea herbicide that exhibits good safety for wheat but causes a certain degree of damage to subsequent corn in a wheat–corn rotation mode, has been suspended field application in China since 2014. Our previous study found that diethylamino-substituted chlorsulfuron derivatives accelerated the degradation rate in soil. In order to obtain sulfonylurea herbicides with good crop safety for both wheat and corn, while maintaining high herbicidal activities, a series of pyrimidine- and triazine-based diethylamino-substituted chlorsulfuron derivatives (W102–W111) wer
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Feng, Tong, Qing Liu, Zhi-Yuan Xu, et al. "Design, Synthesis, Herbicidal Activity, and Structure–Activity Relationship Study of Novel 6-(5-Aryl-Substituted-1-Pyrazolyl)-2-Picolinic Acid as Potential Herbicides." Molecules 28, no. 3 (2023): 1431. http://dx.doi.org/10.3390/molecules28031431.

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Picolinic acid and picolinate compounds are a remarkable class of synthetic auxin herbicides. In recent years, two new picolinate compounds, halauxifen-methyl (ArylexTM active) and florpyrauxifen-benzyl (RinskorTM active), have been launched as novel herbicides. Using their structural skeleton as a template, 33 4-amino-3,5-dicholor-6-(5-aryl-substituted-1-pytazolyl)-2-picolinic acid compounds were designed and synthesized for the discovery of compounds with potent herbicidal activity. The compounds were tested for inhibitory activity against the growth of Arabidopsis thaliana roots, and the re
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Cai, Zengfei, Wenliang Zhang, Zhongjie Yan, and Xiaohua Du. "Synthesis of Novel Pyrazole Derivatives Containing Phenylpyridine Moieties with Herbicidal Activity." Molecules 27, no. 19 (2022): 6274. http://dx.doi.org/10.3390/molecules27196274.

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To discover new compounds with favorable herbicidal activity, a range of phenylpyridine moiety-containing pyrazole derivatives were designed, synthesized, and identified via NMR and HRMS. Their herbicidal activities against six species of weeds were evaluated in a greenhouse via both pre- and post-emergence treatments at 150 g a.i./hm2. The bioassay revealed that a few compounds exhibited moderate herbicidal activities against Digitaria sanguinalis, Abutilon theophrasti, and Setaria viridis in post-emergence treatment. For instance, compounds 6a and 6c demonstrated 50% inhibition activity agai
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Ikeguchi, Masahiko, Masahiko Sawaki, Hitoshi Nakayama, Hiroshi Kikugawa, and Hiroshi Yoshii. "Synthesis and herbicidal activity of new oxazinone herbicides with a long-lasting herbicidal activity againstEchinochloa oryzicola." Pest Management Science 60, no. 10 (2004): 981–91. http://dx.doi.org/10.1002/ps.900.

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SUNITA, SHARMA, and BHATIA M.S. "Synthesis of 2-Cyano-3-(methoxy-substituted-phenyl)acrylamides as Herbicides." Journal of Indian Chemical Society Vol. 68, Nov 1991 (1991): 612–14. https://doi.org/10.5281/zenodo.6136872.

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Department of Chemistry, Punjab Agricultural University,Ludhiana-141 004 <em>Manuscript received 14 September 1990,</em><em>revised 23 August 1991, accepted 28 October 1991</em> Synthesis of 2-Cyano-3-(methoxy-substituted-phenyl)acrylamides as Herbicides. &nbsp;
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Gao, Wei, Xiaotian Li, Da Ren, et al. "Design and Synthesis of N-phenyl Phthalimides as Potent Protoporphyrinogen Oxidase Inhibitors." Molecules 24, no. 23 (2019): 4363. http://dx.doi.org/10.3390/molecules24234363.

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Protoporphyrinogen oxidase (PPO) has been identified as one of the most promising targets for herbicide discovery. A series of novel phthalimide derivatives were designed by molecular docking studies targeting the crystal structure of mitochondrial PPO from tobacco (mtPPO, PDB: 1SEZ) by using Flumioxazin as a lead, after which the derivatives were synthesized and characterized, and their herbicidal activities were subsequently evaluated. The herbicidal bioassay results showed that compounds such as 3a (2-(4-bromo-2,6-difluorophenyl) isoindoline-1,3-dione), 3d (methyl 2-(4-chloro-1,3-dioxoisoin
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Wang, Chaochao, Ke Chen, Na Li, et al. "Design, Synthesis, Mode of Action and Herbicidal Evaluation of Quinazolin-4(3H)-one Derivatives Based on Aryloxyphenoxypropionate Motif." Agronomy 12, no. 8 (2022): 1840. http://dx.doi.org/10.3390/agronomy12081840.

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To discover new acetyl-CoA carboxylase (ACCase) inhibiting-based herbicides, twenty-nine novel quinazolin-4(3H)-one derivatives were designed and synthesized based on the aryloxyphenoxypropionate motif. The bioassay results showed that most of the target compounds showed better pre-emergent herbicidal activity against monocotyledonous weeds in a greenhouse. Especially, when applied at 375 g ha−1 under pre-emergence conditions, compound QPP-7 displayed excellent herbicidal activity against monocotyledonous weeds (i.e., E. crusgalli, D. sanguinalis, P. alopecuroides, S. viridis, E. indica, A. fa
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Dissertations / Theses on the topic "Synthesis and Herbicidal Activity"

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Piunova, Victoria. "Photopolymerizable "Roundup" synthesis, herbicidal activity and coating formulation." Connect to this title online, 2006. http://rave.ohiolink.edu/etdc/view?acc%5Fnum=bgsu1151340117.

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Piunova, Victoria A. "Photopolymerizable “Roundup” Synthesis, Herbicidal Activity and Coating Formulation." Bowling Green State University / OhioLINK, 2006. http://rave.ohiolink.edu/etdc/view?acc_num=bgsu1151340117.

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Murai, Shigeo. "Synthesis and Herbicidal Activity of Nicosulfuron, A New Herbicide for Corn, and Its Related Compounds." Kyoto University, 1998. http://hdl.handle.net/2433/182414.

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CHAKOR, JYOTSNA NARAYAN. "SYNTHESIS AND BIOLOGICAL ACTIVITY EVALUATION OF NATURAL PRODUCTS AND THEIR ANALOGUES." Doctoral thesis, Università degli Studi di Milano, 2010. http://hdl.handle.net/2434/150172.

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The aim of the thesis entitled “Synthesis and biological activity evaluation of natural products and their analogues” is to synthesize some natural products and their analogues in order to study SAR and evaluate their biological activity as fungicides or herbicides. The thesis reports the first enantioselective synthesis of crassinervic acid in 12 steps and 11.8% overall yield. Crassinervic acid, recently isolated from leaves of Piper crassinervium by Kato and co-workers, shows high antifungal activity mainly against Cladosporium cladosporioides and Cladosporium sphaerospermum (minimum amoun
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Coquin, Laurence. "Synthesis and biological activity of heterocycles and heptapeptide derivatives related to microcin B17 : potential leads for new herbicides and antibiotics." Thesis, University of East Anglia, 2005. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.426422.

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Eleftherohorinds, I. G. "Studies on the herbicidal activity of chlorsulfuron." Thesis, University of Reading, 1985. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.354962.

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Osabe, Hirokazu. "Quantitative Structure-Activity Studies of Light-dependent Herbicidal Pyridone-Carboxanilides." Kyoto University, 1992. http://hdl.handle.net/2433/85053.

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McFadden, Helen Georgina, and n/a. "Synthesis and herbicidal properties of some pyrazole and pyrimidine heteocycles." University of Canberra. Biomedical Sciences, 1992. http://erl.canberra.edu.au./public/adt-AUC20060918.160845.

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Four main series of novel heterocyclic compounds were successfully syniliesised. Two of these series were found to be post-emergence herbicides with the activities of each being based on a different mode of action. The (pyrazole-4-yl)alkanones are inhibitors of protoporphyrinogen oxidase, an enzyme in chlorophyll biosynthesis, whereas alkyl 3-arylsulfonylamino- 3-methyllhio-2-(pyrimidin-2-ylcarbamoyl)acrylates and pyrimidin-2-yl 3-(2- chlorophenyl)sulfonyl-amino-3-methylthio-2-cyanoacrylamides (collectively termed "vinylogous sulfonylureas") are inhibitors of acetohydroxy acid synthase (AHAS).
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Jouini, Amira. "Herbicidal activity of Mediterranean essential oils and their effects on soil bioindicators." Doctoral thesis, Universitat Politècnica de València, 2021. http://hdl.handle.net/10251/159914.

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[ES] Las preocupaciones ambientales y de salud han estimulado el interés en estrategias alternativas para el manejo de las malas hierbas. En todo el mundo se están haciendo esfuerzos para reducir la gran dependencia de los herbicidas sintéticos que se utilizan como principal método para el control de las plantas arvenses. Los herbicidas naturales basados en sustancias alelopáticas, como los aceites esenciales (AEs) extraídos de plantas, se han sugerido como una de las posibles alternativas para lograr un manejo sostenible de las arvenses. Por un lado, los AEs han mostrado capacidad para inhibi
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JOUINI, AMIRA. "Herbicidal activity of Mediterranean essential oils and their effects on soil bioindicators." Doctoral thesis, Università degli Studi di Palermo, 2020. http://hdl.handle.net/10447/434529.

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Environmental and health concerns caused for traditional crop protection systems have stimulated interest in alternative weed management strategies. Worldwide, efforts are being made to reduce the heavy reliance on synthetic herbicides that are used to control weeds. Natural herbicides based on allelopathic substances, such as volatile essential oils (EOs) extracted from plants, has been suggested to be one of the possible alternatives for achieving sustainable weed management. From one hand, EOs have shown ability to inhibit weeds seed germination and growth, on the other hand there is a lack
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Books on the topic "Synthesis and Herbicidal Activity"

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J, Wiswesser William, and United States. Agricultural Research Service, eds. A summary of results on 31,000 compounds evaluated for herbicidal activity. U.S. Dept. of Agriculture, Agricultural Research Service, 1987.

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1949-, Basava Channa, and Anantharamaiah G. M. 1947-, eds. Peptides: Design, synthesis, and biological activity. Birkhäuser, 1994.

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Sidney, Udenfriend, and Meienhofer Johannes, eds. The Peptides: Analysis, synthesis, biology. Academic Press, 1987.

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Giltrap, Andrew. Total Synthesis of Natural Products with Antimicrobial Activity. Springer Singapore, 2018. http://dx.doi.org/10.1007/978-981-10-8806-3.

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Stig, Lindholm. Design, synthesis, and antibacterial activity of some pyridylguanidines. Suomalainen Tiedeakatemia, 1990.

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Spitz, William. Airport aviation activity forecasting: A synthesis of airport practice. Transportation Research Board, 2007.

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Royal Society of Chemistry (Great Britain), ed. Polymeric materials with antimicrobial activity: From synthesis to applications. RSC Publishing, 2014.

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Spiers, Ian David. Synthesis, crystallography and biological activity of myo-inositol phosphates. Aston University.Department of Pharmaceutical and Biological Sciences, 1996.

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universitet, Uppsala, ed. Serotonergic 2-Aminotetralin derivatives: Synthesis and structure-activity relationships. Acta Universitatis Upsaliensis, 1994.

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Isaac, J. Structure/activity relationship of Cu/ZnO/Al203 methanol synthesis catalysts. UMIST, 1997.

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Book chapters on the topic "Synthesis and Herbicidal Activity"

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Makino, Kenzi, Katsushi Morimoto, Shigeaki Akiyama, et al. "Synthesis and Herbicidal Activity of Sultamsulfonamides." In ACS Symposium Series. American Chemical Society, 1995. http://dx.doi.org/10.1021/bk-1995-0584.ch003.

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Finn, John, Nina Quinn, and Brad Buckman. "Synthesis and Herbicidal Activity of Pyrrolopyridylimidazolinones." In ACS Symposium Series. American Chemical Society, 1991. http://dx.doi.org/10.1021/bk-1991-0443.ch011.

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Artz, Steven P., Bruce L. Finkelstein, Mary Ann Hanagan, M. P. Moon, Robert J. Pasteris, and Morris P. Rorer. "Synthesis and Herbicidal Activity of Bicyclic Sulfonylureas." In ACS Symposium Series. American Chemical Society, 1991. http://dx.doi.org/10.1021/bk-1991-0443.ch004.

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Karp, Gary M., A. Don Crews, Mark C. Manfredi, et al. "3-(Heterocyclyl)phenyl Cyanurates: Synthesis and Herbicidal Activity." In ACS Symposium Series. American Chemical Society, 2001. http://dx.doi.org/10.1021/bk-2002-0800.ch004.

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Condo, M. E., T. E. Brady, D. Feist, et al. "Synthesis and Herbicidal Activity of 2-Alkylcarbonylphenyl Sulfamoylureas." In ACS Symposium Series. American Chemical Society, 1998. http://dx.doi.org/10.1021/bk-1998-0686.ch010.

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Theodoridis, George, Jonathan S. Baum, Jun H. Chang, et al. "Synthesis and Herbicidal Activity of Fused Benzoheterocyclic Ring Systems." In ACS Symposium Series. American Chemical Society, 1998. http://dx.doi.org/10.1021/bk-1998-0686.ch008.

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Thompson, Mark E., and Paul H. Liang. "Synthesis and Herbicidal Activity of Conformationally Restricted Butyrolactone Sulfonylureas." In ACS Symposium Series. American Chemical Society, 1991. http://dx.doi.org/10.1021/bk-1991-0443.ch007.

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Turner, James A. "Synthesis and Herbicidal Activity of 1,X-Naphthyridinyloxphenoxypropanoic Acids." In ACS Symposium Series. American Chemical Society, 1991. http://dx.doi.org/10.1021/bk-1991-0443.ch017.

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Crews, A. D., M. E. Condon, and M. C. Manfredi. "Synthesis and Herbicidal Activity of Aryloxyphenyl and Heterocyclic Substituted PhenylN-Arylbenzotriazoles." In ACS Symposium Series. American Chemical Society, 1998. http://dx.doi.org/10.1021/bk-1998-0686.ch006.

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Karp, Gary M., Mark C. Manfredi, Michael A. Guaciaro, et al. "1H-1,4-Benzodiazepine-25-diones and Related Systems: Synthesis and Herbicidal Activity." In ACS Symposium Series. American Chemical Society, 1998. http://dx.doi.org/10.1021/bk-1998-0686.ch011.

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Conference papers on the topic "Synthesis and Herbicidal Activity"

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Musiol, Robert, Josef Jampilek, Katarina Kralova, et al. "New Quinoline Derivatives Possessing Herbicidal Activity." In The 9th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2005. http://dx.doi.org/10.3390/ecsoc-9-01508.

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Jampilek, Josef, Jiri Kos, Petra Machalova, et al. "Preparation and Herbicidal Activity of Halogenated 8-Hydroxyquinoline-2-carboxanilides." In The 17th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2013. http://dx.doi.org/10.3390/ecsoc-17-b013.

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Pyrko, A. N. "ENVIRONMENTALLY FRIENDLY SYNTHESIS AND BIOLOGICAL TESTING FOR PESTICIDAL ACTIVITY OF HETEROCYCLIC ANALOGS OF STEROIDS." In SAKHAROV READINGS 2022: ENVIRONMENTAL PROBLEMS OF THE XXI CENTURY. International Sakharov Environmental Institute of Belarusian State University, 2022. http://dx.doi.org/10.46646/sakh-2022-1-187-190.

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The aim of the study is the synthesis and testing for pesticidal activities of 2,3-dimethoxy-16,16-dimethyl-D-homo-8-azagona-1,3,5 (10),13-tetraene-12,17а-one and 2,3-dimethoxy-16,16-dimethyl-d-homo-8-azagona-1,3,5(10),13-tetraene-12-imino-17а-one hydrochloride which could become the basis of plant protection products. The first compound was obtained by condensation of 6,7-dimethoxy-2,3-dihydroisoquinoline with 2-acetyl-5.5-dimethylcyclohexane-1,3-dione. The second substance was synthesized by interaction of the first with ammonium chloride. The synthesized compounds were tested for certain ty
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Dotsenko, Victor, Ilya Ukrainets, Dmitry Tebiev, Vladimir Strelkov, Lyudmila Dyadyuchenko, and Gennady Krapivin. "Synthesis, plant growth regulating activity and herbicide antidote activity of new pyrano[2,3-d]pyrimidines." In The 20th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2016. http://dx.doi.org/10.3390/ecsoc-20-a048.

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Blázquez, M. Amparo, and M. Dolores Ibáñez. "Post-emergence herbicidal activity of Eucalyptus globulus Labill. essential oil." In MOL2NET 2018, International Conference on Multidisciplinary Sciences, 4th edition. MDPI, 2018. http://dx.doi.org/10.3390/mol2net-04-05374.

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Rojas, Sara, Samuel Morales-Cámara, MCarmen Contreras, Pablo Salcedo-Abraria, and Antonio Rodríguez-Diéguez. "Developing novel agrochemical-based MOFs: a multifunctional platform with herbicidal and antibacterial activity." In MATSUS Spring 2025 Conference. FUNDACIO DE LA COMUNITAT VALENCIANA SCITO, 2024. https://doi.org/10.29363/nanoge.matsusspring.2025.446.

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Teja, G. Lakshmi, P. Siva Sankar, N. Bakthavatchala Reddy, V. Padmavathi, and Grigory V. Zyryanov. "Synthesis and antimicrobial activity of spiroheterocycles." In PROCEEDINGS OF THE 3RD INTERNATIONAL CONFERENCE ON AUTOMOTIVE INNOVATION GREEN ENERGY VEHICLE: AIGEV 2018. Author(s), 2019. http://dx.doi.org/10.1063/1.5087391.

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"Plan Synthesis for Probabilistic Activity Recognition." In International Conference on Agents and Artificial Intelligence. SciTePress - Science and and Technology Publications, 2013. http://dx.doi.org/10.5220/0004256002830288.

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Basha, N. Hussain, T. Rekha, G. Sravya, N. Bakthavatchala Reddy, Grigory V. Zyryanov, and V. Padmavathi. "Azolyl pyrimidines-synthesis and antimicrobial activity." In ACTUAL PROBLEMS OF ORGANIC CHEMISTRY AND BIOTECHNOLOGY (OCBT2020): Proceedings of the International Scientific Conference. AIP Publishing, 2022. http://dx.doi.org/10.1063/5.0070395.

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Annuur, Rose Malina, Dyah Ayu Titisari, Rahma Rahayu Dinarlita, et al. "Synthesis and anti-tuberculosis activity of trisindolines." In THE 3RD INTERNATIONAL SEMINAR ON CHEMISTRY: Green Chemistry and its Role for Sustainability. Author(s), 2018. http://dx.doi.org/10.1063/1.5082493.

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Reports on the topic "Synthesis and Herbicidal Activity"

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Atassi, M. Z. Synthesis and Activity of Oxygen-Carrying Heme Peptides. Defense Technical Information Center, 2004. http://dx.doi.org/10.21236/ada428126.

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Katz, Christopher E., and Jeffrey Aube. Synthesis, Conformational Analysis, and Biological Activity of Proposed Vitronectin Antagonists. Defense Technical Information Center, 2001. http://dx.doi.org/10.21236/ada395699.

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Avery, Mitchell A. Drug Development of the Antimalarial Agent Artemisinin: Total Synthesis, Analog Synthesis, and Structure-Activity Relationship Studies. Defense Technical Information Center, 1990. http://dx.doi.org/10.21236/adb152141.

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Granot, David, Scott Holaday, and Randy D. Allen. Enhancing Cotton Fiber Elongation and Cellulose Synthesis by Manipulating Fructokinase Activity. United States Department of Agriculture, 2008. http://dx.doi.org/10.32747/2008.7613878.bard.

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a. Objectives (a) Identification and characterization of the cotton fiber FRKs; (b) Generating transgenic cotton plants overproducing either substrate inhibited tomato FRK or tomato FRK without substrate inhibition; (c) Generating transgenic cotton plants with RNAi suppression of fiber expressed FRKs; (d) Generating Arabidopsis plants that over express FRK1, FRK2, or both genes, as additional means to assess the contribution of FRK to cellulose synthesis and biomass production. b. Background to the topic: Cellulose synthesis and fiber elongation are dependent on sugar metabolism. Previous resu
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Archer, Sydney. Synthesis of 1-(Aminoalkylamino)-3,4-Dimethoxynaphthalenes As Antimalaria Agents with Radical Curative Activity. Defense Technical Information Center, 1988. http://dx.doi.org/10.21236/ada197501.

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Walker, Richard T. Synthesis of Nucleoside Analogues with Potential Antiviral Activity against Negative Strand RNA Virus Targets. Defense Technical Information Center, 1989. http://dx.doi.org/10.21236/ada229411.

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Assabumrungrat, Suttichai, and Bunjerd Jongsomjit. Direct synthesis of Isobutene from CO Hydrogenation with ZrO [subscript 2] catalysts. Chulalongkorn University, 2007. https://doi.org/10.58837/chula.res.2007.76.

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The focus of this research was to investigate the catalytic performances of various zirconia catalysts on isosynthesis. The characteristics of the catalysts were determined by means of various techniques including BET surface area, XRD, NH[[subscript 3][superscript -]] and CO[[subscript 2][superscript -]] TPD, TEM and SEM/EDX. In the first portion, different micron- and nanoscale zirconia catalysts were employed for the isosynthesis and compared with those of ceria. It was found that the nanoscale catalysts showed higher activity and selectivity of isobutene in hydrocarbons than the micronscal
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Eom, Tae-Kil, Ekyune Kim, and Ju-Sung Kim. Inhibitory Effects of 6,6′‑bieckol from Ishige okamurae on Tyrosinase Activity and Melanin Synthesis in Mouse B16F10 Melanoma Cells. "Prof. Marin Drinov" Publishing House of Bulgarian Academy of Sciences, 2019. http://dx.doi.org/10.7546/crabs.2019.09.18.

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Campbell, J. E., I. McMartin, M W McCurdy, et al. Field data and till composition in the GEM-2 Rae Glacial Synthesis Activity field areas, Nunavut and Northwest Territories. Natural Resources Canada/CMSS/Information Management, 2021. http://dx.doi.org/10.4095/328454.

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Meeks, John C. Systems Level Approaches to Understanding and Manipulating Heterocyst Differentiation in Nostoc Punctiforme: Sites of Hydrogenase and Nitrogenase Synthesis and Activity. Office of Scientific and Technical Information (OSTI), 2015. http://dx.doi.org/10.2172/1177288.

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