Статті в журналах з теми "Natural Products - Carbocyclic compounds"
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Banwell, MG. "New Methods for the Synthesis of Troponoid Compounds." Australian Journal of Chemistry 44, no. 1 (1991): 1. http://dx.doi.org/10.1071/ch9910001.
Повний текст джерелаSchmiedel, Volker Martin, and Hans-Ulrich Reissig. "Alkoxyallenes as Starting Materials for the Syntheses of Natural Products." Current Organic Chemistry 23, no. 27 (January 15, 2020): 2976–3003. http://dx.doi.org/10.2174/1385272824666191218115731.
Повний текст джерелаMandal, Sumana, Raju D. Chaudhari, and Goutam Biswas. "Advances in mercury(II)-salt-mediated cyclization reactions of unsaturated bonds." Beilstein Journal of Organic Chemistry 17 (September 9, 2021): 2348–76. http://dx.doi.org/10.3762/bjoc.17.153.
Повний текст джерелаYan, Ning, Yongmei Du, Xinmin Liu, Hongbo Zhang, Yanhua Liu, and Zhongfeng Zhang. "A Review on Bioactivities of Tobacco Cembranoid Diterpenes." Biomolecules 9, no. 1 (January 16, 2019): 30. http://dx.doi.org/10.3390/biom9010030.
Повний текст джерелаMhaske, Santosh, and Ranjeet Dhokale. "Transition-Metal-Catalyzed Reactions Involving Arynes." Synthesis 50, no. 01 (November 22, 2017): 1–16. http://dx.doi.org/10.1055/s-0036-1589517.
Повний текст джерелаChen, Xuefei, Min Xu, Jin Lü, Jianguo Xu, Yemin Wang, Shuangjun Lin, Zixin Deng, and Meifeng Tao. "Biosynthesis of Tropolones inStreptomycesspp.: Interweaving Biosynthesis and Degradation of Phenylacetic Acid and Hydroxylations on the Tropone Ring." Applied and Environmental Microbiology 84, no. 12 (April 13, 2018): e00349-18. http://dx.doi.org/10.1128/aem.00349-18.
Повний текст джерелаOkumura, Mikiko, and David Sarlah. "Arenophile-Mediated Photochemical Dearomatization of Nonactivated Arenes." CHIMIA International Journal for Chemistry 74, no. 7 (August 12, 2020): 577–83. http://dx.doi.org/10.2533/chimia.2020.577.
Повний текст джерелаSmyrniotopoulos, Vangelis, Anna Cláudia de Andrade Tomaz, Maria de Fátima Vanderlei de Souza, Emídio Vasconcelos Leitão da Cunha, Robert Kiss, Véronique Mathieu, Efstathia Ioannou, and Vassilios Roussis. "Halogenated Diterpenes with In Vitro Antitumor Activity from the Red Alga Sphaerococcus coronopifolius." Marine Drugs 18, no. 1 (December 29, 2019): 29. http://dx.doi.org/10.3390/md18010029.
Повний текст джерелаTammam, Mohamed A., Lucie Rárová, Marie Kvasnicová, Gabriel Gonzalez, Ahmed M. Emam, Aldoushy Mahdy, Miroslav Strnad, Efstathia Ioannou, and Vassilios Roussis. "Bioactive Steroids from the Red Sea Soft Coral Sinularia polydactyla." Marine Drugs 18, no. 12 (December 10, 2020): 632. http://dx.doi.org/10.3390/md18120632.
Повний текст джерелаYang, Ji-Min, Yu-Kun Lin, Tao Sheng, Liang Hu, Xin-Pei Cai, and Jin-Quan Yu. "Regio-controllable [2+2] benzannulation with two adjacent C(sp 3 )–H bonds." Science 380, no. 6645 (May 12, 2023): 639–44. http://dx.doi.org/10.1126/science.adg5282.
Повний текст джерелаRiley, Dean A., Nigel S. Simpkins, and David Moffat. "Synthesis of novel carbocyclic analogues of indolocarbazole natural products." Tetrahedron Letters 40, no. 20 (May 1999): 3929–32. http://dx.doi.org/10.1016/s0040-4039(99)00572-9.
Повний текст джерелаWright, Austin C., and Brian M. Stoltz. "Enantioselective construction of the tricyclic core of curcusones A–D via a cross-electrophile coupling approach." Chemical Science 10, no. 45 (2019): 10562–65. http://dx.doi.org/10.1039/c9sc04127c.
Повний текст джерелаChen, Houguang Jeremy, Ronald Hong Xiang Teo, Jonathan Wong, Yongxin Li, Sumod A. Pullarkat та Pak-Hing Leung. "Challenges in cyclometalation: steric effects leading to competing pathways and η1,η2-cyclometalated iridium(iii) complexes". Dalton Transactions 47, № 37 (2018): 13046–51. http://dx.doi.org/10.1039/c8dt02639d.
Повний текст джерелаBlunt, John W., Brent R. Copp, Robert A. Keyzers, Murray H. G. Munro, and Michèle R. Prinsep. "Marine natural products." Natural Product Reports 33, no. 3 (2016): 382–431. http://dx.doi.org/10.1039/c5np00156k.
Повний текст джерелаBlunt, John W., Brent R. Copp, Robert A. Keyzers, Murray H. G. Munro, and Michèle R. Prinsep. "Marine natural products." Natural Product Reports 32, no. 2 (2015): 116–211. http://dx.doi.org/10.1039/c4np00144c.
Повний текст джерелаBlunt, John W., Brent R. Copp, Robert A. Keyzers, Murray H. G. Munro, and Michèle R. Prinsep. "Marine natural products." Natural Product Reports 34, no. 3 (2017): 235–94. http://dx.doi.org/10.1039/c6np00124f.
Повний текст джерелаLiu, Yuxiao, Yu Liu, Charles S. Shanahan, Xichen Xu, and Michael P. Doyle. "A survey of enoldiazo nucleophilicity in selective C–C bond forming reactions for the synthesis of natural product-like frameworks." Org. Biomol. Chem. 12, no. 28 (2014): 5227–34. http://dx.doi.org/10.1039/c4ob00709c.
Повний текст джерелаCarroll, Anthony R., Brent R. Copp, Rohan A. Davis, Robert A. Keyzers, and Michèle R. Prinsep. "Marine natural products." Natural Product Reports 37, no. 2 (2020): 175–223. http://dx.doi.org/10.1039/c9np00069k.
Повний текст джерелаAimon, Anthony, Louis J. Farrugia, and J. Stephen Clark. "Synthesis of the Core Framework of the Cornexistins by Intramolecular Nozaki-Hiyama-Kishi Coupling." Molecules 24, no. 14 (July 22, 2019): 2654. http://dx.doi.org/10.3390/molecules24142654.
Повний текст джерелаDuke, Stephen O., and John Lydon. "Herbicides from Natural Compounds." Weed Technology 1, no. 2 (April 1987): 122–28. http://dx.doi.org/10.1017/s0890037x00029304.
Повний текст джерелаSoós, Tibor, Dániel Horváth, Frigyes Domonyi, Roberta Palkó, and Andrea Lomoschitz. "Regioexhaustive Functionalization of the Carbocyclic Core of Isoquinoline: Concise Synthesis of Oxoaporphine Core and Ellipticine." Synthesis 50, no. 11 (March 7, 2018): 2181–90. http://dx.doi.org/10.1055/s-0037-1609153.
Повний текст джерелаArciszewska, Karolina, Anna Pućkowska, Agnieszka Wróbel, and Danuta Drozdowska. "Carbocyclic Analogues of Distamycin and Netropsin." Mini-Reviews in Medicinal Chemistry 19, no. 2 (December 6, 2018): 98–113. http://dx.doi.org/10.2174/1389557518666181009143203.
Повний текст джерелаCekovic, Zivorad. "Natural products for plant protection." Chemical Industry 60, no. 5-6 (2006): 113–19. http://dx.doi.org/10.2298/hemind0606113c.
Повний текст джерелаKayser, Oliver, K. Noël Masihi, and Albrecht F. Kiderlen. "Natural products and synthetic compounds as immunomodulators." Expert Review of Anti-infective Therapy 1, no. 2 (July 2003): 319–35. http://dx.doi.org/10.1586/14787210.1.2.319.
Повний текст джерелаBarnes, Jo. "Novel compounds in development from natural products." Inpharma Weekly &NA;, no. 1011 (November 1995): 3–4. http://dx.doi.org/10.2165/00128413-199510110-00003.
Повний текст джерелаEgu, Samuel Attah, Efeturi Abraham Onoabedje, Uchechukwu Chris Okoro, Khalid Mohammed Khan, Abdul Hameed, Irfan Ali, Shafia Iftekhar, Eboh Monday Odin, and Shahbaz Shamim. "The Synthesis and Chemistry of Quinolinediones and their Carbocyclic Analogs." Mini-Reviews in Organic Chemistry 19, no. 5 (August 2022): 591–607. http://dx.doi.org/10.2174/1570193x18666211007120708.
Повний текст джерелаBattiste, Merle A., Phillip M. Pelphrey, and Dennis L. Wright. "The Cycloaddition Strategy for the Synthesis of Natural Products Containing Carbocyclic Seven-Membered Rings." Chemistry - A European Journal 12, no. 13 (April 24, 2006): 3438–47. http://dx.doi.org/10.1002/chem.200501083.
Повний текст джерелаQiu, Rongxiang. "Applications of transition state calculations in the key cyclization of small molecule natural product synthesis." E3S Web of Conferences 290 (2021): 01024. http://dx.doi.org/10.1051/e3sconf/202129001024.
Повний текст джерелаEisenreich, Andreas, and Bernd Schäfer. "Natural Compounds in Plant-Based Food." Foods 12, no. 4 (February 17, 2023): 857. http://dx.doi.org/10.3390/foods12040857.
Повний текст джерелаRoberts, S. M., and N. M. Williamson. "The Use of Enzymes for the Preparation of Biologically Active Natural Products and Analogues in Optically Active Form." Current Organic Chemistry 1, no. 1 (May 1997): 1–20. http://dx.doi.org/10.2174/1385272801666220121181731.
Повний текст джерелаvan Santen, Jeffrey A., Ella F. Poynton, Dasha Iskakova, Emily McMann, Tyler A. Alsup, Trevor N. Clark, Claire H. Fergusson, et al. "The Natural Products Atlas 2.0: a database of microbially-derived natural products." Nucleic Acids Research 50, no. D1 (October 28, 2021): D1317—D1323. http://dx.doi.org/10.1093/nar/gkab941.
Повний текст джерелаWang, Lishu, Jungfeng Wang, Juan Liu, and Yonghong Liu. "Antitubercular Marine Natural Products." Current Medicinal Chemistry 25, no. 20 (June 14, 2018): 2304–28. http://dx.doi.org/10.2174/0929867324666170113120221.
Повний текст джерелаOrtiz, Aurelio, and Estibaliz Sansinenea. "Macrolactin Antibiotics: Amazing Natural Products." Mini-Reviews in Medicinal Chemistry 20, no. 7 (May 18, 2020): 584–600. http://dx.doi.org/10.2174/1389557519666191205124050.
Повний текст джерелаReeves, Ryan D., Caitlin N. Kinkema, Eleanor M. Landwehr, Logan E. Vine, and Jennifer M. Schomaker. "Stereodivergent Metal-Catalyzed Allene Cycloisomerizations." Synlett 31, no. 06 (February 4, 2020): 627–31. http://dx.doi.org/10.1055/s-0037-1610746.
Повний текст джерелаRajčević, Nemanja, Danka Bukvički, Tanja Dodoš, and Petar D. Marin. "Interactions between Natural Products—A Review." Metabolites 12, no. 12 (December 14, 2022): 1256. http://dx.doi.org/10.3390/metabo12121256.
Повний текст джерелаKrivdin, Leonid, and Valentin Semenov. "COMPUTATIONAL NMR OF NATURAL PRODUCTS." Modern Technologies and Scientific and Technological Progress 1, no. 1 (May 17, 2021): 38–39. http://dx.doi.org/10.36629/2686-9896-2021-1-1-38-39.
Повний текст джерелаModugu, Nagi Reddy, and Goverdhan Mehta. "An approach toward novel bioactive natural products antroquinonols: de novo construction of the carbocyclic core." Tetrahedron Letters 56, no. 44 (October 2015): 6030–33. http://dx.doi.org/10.1016/j.tetlet.2015.09.043.
Повний текст джерелаHaque, Neshatul, Sana Parveen, Tingting Tang, Jiaen Wei, and Zunnan Huang. "Marine Natural Products in Clinical Use." Marine Drugs 20, no. 8 (August 18, 2022): 528. http://dx.doi.org/10.3390/md20080528.
Повний текст джерелаMaltese, Federica, Frank van der Kooy, and Robert Verpoorte. "Solvent Derived Artifacts in Natural Products Chemistry." Natural Product Communications 4, no. 3 (March 2009): 1934578X0900400. http://dx.doi.org/10.1177/1934578x0900400326.
Повний текст джерелаKitamura, Masato, Kengo Miyata, Tomoaki Seki, Namdev Vatmurge, and Shinji Tanaka. "CpRu-catalyzed asymmetric dehydrative allylation." Pure and Applied Chemistry 85, no. 6 (April 15, 2013): 1121–32. http://dx.doi.org/10.1351/pac-con-12-10-02.
Повний текст джерелаNora De Souza, Marcus Vinícius. "Marine Natural Products Against Tuberculosis." Scientific World JOURNAL 6 (2006): 847–61. http://dx.doi.org/10.1100/tsw.2006.174.
Повний текст джерелаLaudato, Massimiliano, Luigi Pescitelli, and Raffaele Capasso. "Natural Products of Mineral Origin." Natural Product Communications 8, no. 3 (March 2013): 1934578X1300800. http://dx.doi.org/10.1177/1934578x1300800336.
Повний текст джерелаChua, Lee Suan. "Bioactive compounds from natural products with antidiabetic potentials." Longhua Chinese Medicine 5 (March 2022): 1. http://dx.doi.org/10.21037/lcm-21-64.
Повний текст джерелаTeuten, E. L. "Two Abundant Bioaccumulated Halogenated Compounds Are Natural Products." Science 307, no. 5711 (February 11, 2005): 917–20. http://dx.doi.org/10.1126/science.1106882.
Повний текст джерелаKhazir, Jabeena, Bilal Ahmad Mir, Shabir Ahmad Mir, and Don Cowan. "Natural products as lead compounds in drug discovery." Journal of Asian Natural Products Research 15, no. 7 (July 2013): 764–88. http://dx.doi.org/10.1080/10286020.2013.798314.
Повний текст джерелаLU, Jin-Jian, and Yi-Tao WANG. "Identification of anti-cancer compounds from natural products." Chinese Journal of Natural Medicines 18, no. 7 (July 2020): 481–82. http://dx.doi.org/10.1016/s1875-5364(20)30057-1.
Повний текст джерелаRomano, Barbara, Asif Jilani Iqbal, and Francesco Maione. "Natural Anti-Inflammatory Products/Compounds: Hopes and Reality." Mediators of Inflammation 2015 (2015): 1–2. http://dx.doi.org/10.1155/2015/374239.
Повний текст джерелаGiles, P. M. "Revised Section F: Natural products and related compounds." Pure and Applied Chemistry 71, no. 4 (January 1, 1999): 587–643. http://dx.doi.org/10.1351/pac199971040587.
Повний текст джерелаParrish, Jonathan D., and R. Daniel Little. "ChemInform Abstract: Natural Products and Medicinally Important Compounds." ChemInform 33, no. 52 (May 18, 2010): no. http://dx.doi.org/10.1002/chin.200252273.
Повний текст джерелаGallo, Monica. "Extraction and Isolation of Natural Products." Separations 9, no. 10 (October 5, 2022): 287. http://dx.doi.org/10.3390/separations9100287.
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