Статті в журналах з теми "Organic synthesis, Catalysis, and methodology development"
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De Vreese, Rob, and Matthias D’hooghe. "N-Heterocyclic carbene/Brønsted acid cooperative catalysis as a powerful tool in organic synthesis." Beilstein Journal of Organic Chemistry 8 (March 14, 2012): 398–402. http://dx.doi.org/10.3762/bjoc.8.43.
Повний текст джерелаDzieszkowski, Krzysztof, and Zbigniew Rafiński. "N-Heterocyclic Carbene Catalysis under Oxidizing Conditions." Catalysts 8, no. 11 (November 16, 2018): 549. http://dx.doi.org/10.3390/catal8110549.
Повний текст джерелаLübken, Dennis, Marius Saxarra, and Markus Kalesse. "Tris(acetylacetonato) Iron(III): Recent Developments and Synthetic Applications." Synthesis 51, no. 01 (November 27, 2018): 161–77. http://dx.doi.org/10.1055/s-0037-1610393.
Повний текст джерелаBiswas, Swapan Kumar. "Recent development of Silver-catalyzed Oxo- and Aza cyclization." International Journal of Experimental Research and Review 26 (December 30, 2021): 90–98. http://dx.doi.org/10.52756/ijerr.2021.v26.007.
Повний текст джерелаKoskinen, Ari M. P. "Chirospecific synthesis: Catalysis and chiral pool hand in hand." Pure and Applied Chemistry 83, no. 3 (January 16, 2011): 435–43. http://dx.doi.org/10.1351/pac-con-10-10-09.
Повний текст джерелаYeung, Ying-Yeung. "Cluster Preface: Organosulfur and Organoselenium Compounds in Catalysis." Synlett 30, no. 14 (August 19, 2019): 1643–45. http://dx.doi.org/10.1055/s-0039-1690021.
Повний текст джерелаCortón, Pablo, Paula Novo, Vanesa López-Sobrado, Marcos D. García, Carlos Peinador, and Elena Pazos. "Solid-Phase Zincke Reaction for the Synthesis of Peptide-4,4′-bipyridinium Conjugates." Synthesis 52, no. 04 (July 30, 2019): 537–43. http://dx.doi.org/10.1055/s-0039-1690016.
Повний текст джерелаKim, Nari, Calvin C. H. Cheng, and M. Cynthia Goh. "Universal aqueous synthesis of ultra-small polymer-templated nanoparticles: synthesis optimization methodology for counterion-collapsed poly(acrylic acid)." Canadian Journal of Chemistry 96, no. 1 (January 2018): 44–50. http://dx.doi.org/10.1139/cjc-2017-0444.
Повний текст джерелаFeng, Liang, Kun-Yu Wang, Xiu-Liang Lv, Tian-Hao Yan, and Hong-Cai Zhou. "Hierarchically porous metal–organic frameworks: synthetic strategies and applications." National Science Review 7, no. 11 (November 5, 2019): 1743–58. http://dx.doi.org/10.1093/nsr/nwz170.
Повний текст джерелаScheffer, John R. "2000 Alfred Bader Award LectureIn the footsteps of Pasteur: asymmetric induction in the photochemistry of crystalline ammonium carboxylate salts." Canadian Journal of Chemistry 79, no. 4 (April 1, 2001): 349–57. http://dx.doi.org/10.1139/v01-060.
Повний текст джерелаKanwal, Iram, Aqsa Mujahid, Nasir Rasool, Komal Rizwan, Ayesha Malik, Gulraiz Ahmad, Syed Adnan Ali Shah, Umer Rashid, and Nadiah Mad Nasir. "Palladium and Copper Catalyzed Sonogashira cross Coupling an Excellent Methodology for C-C Bond Formation over 17 Years: A Review." Catalysts 10, no. 4 (April 20, 2020): 443. http://dx.doi.org/10.3390/catal10040443.
Повний текст джерелаWrzeszcz, Zuzanna, and Renata Siedlecka. "Heteroaromatic N-Oxides in Asymmetric Catalysis: A Review." Molecules 25, no. 2 (January 14, 2020): 330. http://dx.doi.org/10.3390/molecules25020330.
Повний текст джерелаMcMurray, Lindsay, Thomas M. McGuire, and Rachel L. Howells. "Recent Advances in Photocatalytic Decarboxylative Coupling Reactions in Medicinal Chemistry." Synthesis 52, no. 12 (March 9, 2020): 1719–37. http://dx.doi.org/10.1055/s-0039-1690843.
Повний текст джерелаKwon, Kitae, R. Thomas Simons, Meganathan Nandakumar, and Jennifer L. Roizen. "Strategies to Generate Nitrogen-centered Radicals That May Rely on Photoredox Catalysis: Development in Reaction Methodology and Applications in Organic Synthesis." Chemical Reviews 122, no. 2 (October 8, 2021): 2353–428. http://dx.doi.org/10.1021/acs.chemrev.1c00444.
Повний текст джерелаAlbert-Soriano, María, and Isidro M. Pastor. "N,N-Diethyl-3-methylbenzamide." Molbank 2022, no. 3 (June 25, 2022): M1395. http://dx.doi.org/10.3390/m1395.
Повний текст джерелаBortolami, Martina, Ingrid Izabela Bogles, Cecilia Bombelli, Fabiana Pandolfi, Marta Feroci, and Fabrizio Vetica. "Electrochemical Bottom-Up Synthesis of Chiral Carbon Dots from L-Proline and Their Application as Nano-Organocatalysts in a Stereoselective Aldol Reaction." Molecules 27, no. 16 (August 12, 2022): 5150. http://dx.doi.org/10.3390/molecules27165150.
Повний текст джерелаCamp, Jason, Thomas Bousfield, Jay Dunsford, James Adams, Joshua Britton, Michael Fay, and Athanasios Angelis-Dimakis. "Dehydrative Cross-Coupling of 1-Phenylethanol Catalysed by Palladium Nanoparticles Formed in situ Under Acidic Conditions." Synthesis 50, no. 19 (August 27, 2018): 3862–74. http://dx.doi.org/10.1055/s-0037-1610246.
Повний текст джерелаSzadkowska, Anna, Cezary Samojłowicz, and Karol Grela. "Enhancement of ruthenium-catalyzed olefin metathesis reactions: Searching for new catalyst or new reaction conditions?" Pure and Applied Chemistry 83, no. 3 (January 16, 2011): 553–63. http://dx.doi.org/10.1351/pac-con-10-09-10.
Повний текст джерелаLiu, Wenbo, and Chao-Jun Li. "Recent Synthetic Applications of Catalyst-Free Photochemistry." Synlett 28, no. 20 (September 14, 2017): 2714–54. http://dx.doi.org/10.1055/s-0036-1590900.
Повний текст джерелаHuang, Xin, Zengbei Li, Zhengguo Yu, Xinjie Deng, and Yi Xin. "Recent Advances in the Synthesis, Properties, and Biological Applications of Platinum Nanoclusters." Journal of Nanomaterials 2019 (September 8, 2019): 1–31. http://dx.doi.org/10.1155/2019/6248725.
Повний текст джерелаMalkov, Andrei V., and Aleksandr E. Rubtsov. "Developing a Methodology for Catalytic Asymmetric Crotylation of Aldehydes." Synlett 32, no. 14 (January 18, 2021): 1397–405. http://dx.doi.org/10.1055/s-0040-1706659.
Повний текст джерелаHall, Dennis G. "New preparative methods for allylic boronates and their application in stereoselective catalytic allylborations." Pure and Applied Chemistry 80, no. 5 (January 1, 2008): 913–27. http://dx.doi.org/10.1351/pac200880050913.
Повний текст джерелаMyers, Deborah J., Ahmed A. Farghaly, Magali Ferrandon, A. Jeremy Kropf, and David A. Cullen. "Platinum Group Metal-Free Oxygen Evolution Electrocatalysts for Alkaline Water Electrolysis." ECS Meeting Abstracts MA2022-02, no. 44 (October 9, 2022): 1672. http://dx.doi.org/10.1149/ma2022-02441672mtgabs.
Повний текст джерелаRoy, Snigdha. "Prins-Friedel-Crafts Cyclization: Synthesis of Diversely Functionalized Six- Membered Oxacycles." Current Organic Chemistry 25, no. 5 (March 15, 2021): 635–51. http://dx.doi.org/10.2174/1385272825666210114105020.
Повний текст джерелаHiyama, Tamejiro. "Preface." Pure and Applied Chemistry 77, no. 7 (January 1, 2005): iv. http://dx.doi.org/10.1351/pac20057707iv.
Повний текст джерелаKocaarslan, Azra, Zafer Eroglu, Önder Metin, and Yusuf Yagci. "Exfoliated black phosphorous-mediated CuAAC chemistry for organic and macromolecular synthesis under white LED and near-IR irradiation." Beilstein Journal of Organic Chemistry 17 (September 23, 2021): 2477–87. http://dx.doi.org/10.3762/bjoc.17.164.
Повний текст джерелаMoore, Eric J., Dmitri Zorine, William A. Hansen, Sagar D. Khare, and Rudi Fasan. "Enzyme stabilization via computationally guided protein stapling." Proceedings of the National Academy of Sciences 114, no. 47 (November 6, 2017): 12472–77. http://dx.doi.org/10.1073/pnas.1708907114.
Повний текст джерелаMitsudo, Koichi, Yuji Kurimoto, Jun Yamashita, and Seiji Suga. "(Digital Presentation) Electrochemical Dehydrogenative C–P Bond Formation for the Synthesis of Phosphacycles Using DABCO As a Mediator." ECS Meeting Abstracts MA2022-01, no. 42 (July 7, 2022): 1838. http://dx.doi.org/10.1149/ma2022-01421838mtgabs.
Повний текст джерелаWoźny, Mateusz, Adam Mames, and Tomasz Ratajczyk. "Triptycene Derivatives: From Their Synthesis to Their Unique Properties." Molecules 27, no. 1 (December 31, 2021): 250. http://dx.doi.org/10.3390/molecules27010250.
Повний текст джерелаQasim, Muhammad, Andrew N. Clarkson, and Simon F. R. Hinkley. "Green Synthesis of Carbon Nanoparticles (CNPs) from Biomass for Biomedical Applications." International Journal of Molecular Sciences 24, no. 2 (January 5, 2023): 1023. http://dx.doi.org/10.3390/ijms24021023.
Повний текст джерелаLuque-Jacobo, Cristina M., Andrea L. Cespedes-Loayza, Talia S. Echegaray-Ugarte, Jacqueline L. Cruz-Loayza, Isemar Cruz, Júlio Cesar de Carvalho, and Luis Daniel Goyzueta-Mamani. "Biogenic Synthesis of Copper Nanoparticles: A Systematic Review of Their Features and Main Applications." Molecules 28, no. 12 (June 18, 2023): 4838. http://dx.doi.org/10.3390/molecules28124838.
Повний текст джерелаKristensen, Tor E. "Chemoselective O-acylation of hydroxyamino acids and amino alcohols under acidic reaction conditions: History, scope and applications." Beilstein Journal of Organic Chemistry 11 (April 8, 2015): 446–68. http://dx.doi.org/10.3762/bjoc.11.51.
Повний текст джерелаCai, Jiayou, Bin Sun, Siqi Yu, Han Zhang, and Weicheng Zhang. "Heck Macrocyclization in Forging Non-Natural Large Rings including Macrocyclic Drugs." International Journal of Molecular Sciences 24, no. 9 (May 4, 2023): 8252. http://dx.doi.org/10.3390/ijms24098252.
Повний текст джерелаNoor, Rida, Ameer Fawad Zahoor, Muhammad Irfan, Syed Makhdoom Hussain, Sajjad Ahmad, Ali Irfan, Katarzyna Kotwica-Mojzych, and Mariusz Mojzych. "Transition Metal Catalyzed Hiyama Cross-Coupling: Recent Methodology Developments and Synthetic Applications." Molecules 27, no. 17 (September 2, 2022): 5654. http://dx.doi.org/10.3390/molecules27175654.
Повний текст джерелаAkácsos-Szász, Orsolya-Zsuzsa, Sándor Pál, Kinga-Ilona Nyulas, Enikő Nemes-Nagy, Ana-Maria Fárr, Lóránd Dénes, Mónika Szilveszter, Erika-Gyöngyi Bán, Mariana Cornelia Tilinca, and Zsuzsánna Simon-Szabó. "Pathways of Coagulopathy and Inflammatory Response in SARS-CoV-2 Infection among Type 2 Diabetic Patients." International Journal of Molecular Sciences 24, no. 5 (February 21, 2023): 4319. http://dx.doi.org/10.3390/ijms24054319.
Повний текст джерелаSmolskaya, Sviatlana, Yulia A. Logashina, and Yaroslav A. Andreev. "Escherichia coli Extract-Based Cell-Free Expression System as an Alternative for Difficult-to-Obtain Protein Biosynthesis." International Journal of Molecular Sciences 21, no. 3 (January 31, 2020): 928. http://dx.doi.org/10.3390/ijms21030928.
Повний текст джерелаKus-Liśkiewicz, Małgorzata, Patrick Fickers, and Imen Ben Tahar. "Biocompatibility and Cytotoxicity of Gold Nanoparticles: Recent Advances in Methodologies and Regulations." International Journal of Molecular Sciences 22, no. 20 (October 11, 2021): 10952. http://dx.doi.org/10.3390/ijms222010952.
Повний текст джерелаDangi, Hemlata, Atish Roy, Aayushi Chanderiya, Sushil Kashaw, and Ratnesh Das. "One pot synthesis of some novel indole derivatives and their antimicrobial activity." Mediterranean Journal of Chemistry 13, no. 1 (February 3, 2023): 42. http://dx.doi.org/10.13171/mjc02302031664das-dangi.
Повний текст джерелаGabriele, Bartolo. "Organic Synthesis via Transition Metal-Catalysis." Molecules 27, no. 4 (February 11, 2022): 1227. http://dx.doi.org/10.3390/molecules27041227.
Повний текст джерелаMakosza, Mieczyslaw. "Phase-transfer catalysis. A general green methodology in organic synthesis." Pure and Applied Chemistry 72, no. 7 (January 1, 2000): 1399–403. http://dx.doi.org/10.1351/pac200072071399.
Повний текст джерелаDou, Qian, Taimin Wang, Lijing Fang, Hongbin Zhai, and Bin Cheng. "Recent Development of Photoinduced Iron-Catalysis in Organic Synthesis." Chinese Journal of Organic Chemistry 43, no. 4 (2023): 1386. http://dx.doi.org/10.6023/cjoc202209001.
Повний текст джерелаKobayashi, Shū, and Kei Manabe. "Green Lewis acid catalysis in organic synthesis." Pure and Applied Chemistry 72, no. 7 (January 1, 2000): 1373–80. http://dx.doi.org/10.1351/pac200072071373.
Повний текст джерелаLi, Hong-Xi, Da-Liang Zhu, and David James Young. "Carbonyl-Photoredox/Metal Dual Catalysis: Applications in Organic Synthesis." Synthesis 52, no. 23 (July 21, 2020): 3493–510. http://dx.doi.org/10.1055/s-0040-1707183.
Повний текст джерелаMakosza, Mieczyslaw. "ChemInform Abstract: Phase-Transfer Catalysis: A General Green Methodology in Organic Synthesis." ChemInform 32, no. 16 (April 17, 2001): no. http://dx.doi.org/10.1002/chin.200116277.
Повний текст джерелаDaBell, Peter, and Stephen P. Thomas. "Iron Catalysis in Target Synthesis." Synthesis 52, no. 07 (February 5, 2020): 949–63. http://dx.doi.org/10.1055/s-0039-1690813.
Повний текст джерелаBeatty, Joel W., and Corey R. J. Stephenson. "Amine Functionalization via Oxidative Photoredox Catalysis: Methodology Development and Complex Molecule Synthesis." Accounts of Chemical Research 48, no. 5 (May 7, 2015): 1474–84. http://dx.doi.org/10.1021/acs.accounts.5b00068.
Повний текст джерелаISAYAMA, Shigeru. "Development of Novel Methodology in Organic Synthesis Using Cobalt(II) Catalyst." Journal of Synthetic Organic Chemistry, Japan 50, no. 3 (1992): 190–201. http://dx.doi.org/10.5059/yukigoseikyokaishi.50.190.
Повний текст джерелаTian, Wei, and Spiros Grivas. "A Useful Methodology for the Synthesis of 2-Methyl-4-nitrobenzimidazoles." Synthesis 1992, no. 12 (1992): 1283–86. http://dx.doi.org/10.1055/s-1992-26359.
Повний текст джерелаBeeler, Aaron, John Porco Jr., John Goodell, Bo Leng, and Tracy Snyder. "Multidimensional Screening and Methodology Development for Condensations Involving Complex 1,2-Diketones." Synthesis 2010, no. 13 (June 11, 2010): 2254–70. http://dx.doi.org/10.1055/s-0029-1218813.
Повний текст джерелаFilipczak, Nina, Satya Siva Kishan Yalamarty, Xiang Li, Farzana Parveen, and Vladimir Torchilin. "Developments in Treatment Methodologies Using Dendrimers for Infectious Diseases." Molecules 26, no. 11 (May 31, 2021): 3304. http://dx.doi.org/10.3390/molecules26113304.
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