Добірка наукової літератури з теми "Aryls(Heteroaryls) compound"
Оформте джерело за APA, MLA, Chicago, Harvard та іншими стилями
Ознайомтеся зі списками актуальних статей, книг, дисертацій, тез та інших наукових джерел на тему "Aryls(Heteroaryls) compound".
Біля кожної праці в переліку літератури доступна кнопка «Додати до бібліографії». Скористайтеся нею – і ми автоматично оформимо бібліографічне посилання на обрану працю в потрібному вам стилі цитування: APA, MLA, «Гарвард», «Чикаго», «Ванкувер» тощо.
Також ви можете завантажити повний текст наукової публікації у форматі «.pdf» та прочитати онлайн анотацію до роботи, якщо відповідні параметри наявні в метаданих.
Статті в журналах з теми "Aryls(Heteroaryls) compound"
Stefanello, Felipe S., Jean C. B. Vieira, Juliane N. Araújo, Vitória B. Souza, Clarissa P. Frizzo, Marcos A. P. Martins, Nilo Zanatta, Bernardo A. Iglesias, and Helio G. Bonacorso. "Solution and Solid-State Optical Properties of Trifluoromethylated 5-(Alkyl/aryl/heteroaryl)-2-methyl-pyrazolo[1,5-a]pyrimidine System." Photochem 2, no. 2 (May 19, 2022): 345–57. http://dx.doi.org/10.3390/photochem2020024.
Повний текст джерелаShui, Hongling, Yuhong Zhong, Renshi Luo, Zhanyi Zhang, Jiuzhong Huang, Ping Yang, and Nianhua Luo. "Cyclometalated iridium complexes-catalyzed acceptorless dehydrogenative coupling reaction: construction of quinoline derivatives and evaluation of their antimicrobial activities." Beilstein Journal of Organic Chemistry 18 (October 27, 2022): 1507–17. http://dx.doi.org/10.3762/bjoc.18.159.
Повний текст джерелаKalam, Sirisha, Rajyalaxmi I, and Olivia S. "Synthesis and In vitro P-Glycoprotein Inhibitory Activity of Novel 1,4-Dihydropyridine Derivatives." International Journal of Pharmaceutical Sciences and Nanotechnology 7, no. 3 (August 31, 2014): 2544–52. http://dx.doi.org/10.37285/ijpsn.2014.7.3.6.
Повний текст джерелаMarzo, Leyre, Ignacio Pérez, Francisco Yuste, José Alemán, and José Luis García Ruano. "A straightforward alkynylation of Li and Mg metalated heterocycles with sulfonylacetylenes." Chemical Communications 51, no. 2 (2015): 346–49. http://dx.doi.org/10.1039/c4cc07574a.
Повний текст джерелаNarayanaperumal, Senthil, Ricardo S. Schwab, Wystan K. O. Teixeira, and Danilo Yano de Albuquerque. "Recent Advances in the Synthesis of Enantiomerically Enriched Diaryl, Aryl Heteroaryl, and Diheteroaryl Alcohols through Addition of Organometallic Reagents to Carbonyl Compounds." Synthesis 52, no. 13 (March 16, 2020): 1855–73. http://dx.doi.org/10.1055/s-0039-1690847.
Повний текст джерелаSaritha, Rajendhiran, Sesuraj Babiola Annes, Subramanian Saravanan, and Subburethinam Ramesh. "Carbazole based Electron Donor Acceptor (EDA) catalysis for the synthesis of biaryl and aryl–heteroaryl compounds." Organic & Biomolecular Chemistry 18, no. 13 (2020): 2510–15. http://dx.doi.org/10.1039/d0ob00282h.
Повний текст джерелаSitapara, Sachin M., Jignesh H. Pandya, and Chandankumar Pashavan. "An Efficient Synthesis of Novel Triazolo-pyrimidine Derivatives using Copper Catalyzed Click Chemistry (CuAAC) Approach." Asian Journal of Organic & Medicinal Chemistry 7, no. 2 (2022): 153–58. http://dx.doi.org/10.14233/ajomc.2022.ajomc-p378.
Повний текст джерелаGangadurai, Chinnakuzhanthai, Giri Teja Illa, and D. Srinivasa Reddy. "FeCl3-catalyzed oxidative decarboxylation of aryl/heteroaryl acetic acids: preparation of selected API impurities." Organic & Biomolecular Chemistry 18, no. 41 (2020): 8459–66. http://dx.doi.org/10.1039/d0ob01790f.
Повний текст джерелаMalik, Ayesha, Nasir Rasool, Iram Kanwal, Muhammad Ali Hashmi, Ameer Fawad Zahoor, Gulraiz Ahmad, Ataf Ali Altaf, Syed Adnan Ali Shah, Sadia Sultan, and Zainul Amiruddin Zakaria. "Suzuki–Miyaura Reactions of (4-bromophenyl)-4,6-dichloropyrimidine through Commercially Available Palladium Catalyst: Synthesis, Optimization and Their Structural Aspects Identification through Computational Studies." Processes 8, no. 11 (October 23, 2020): 1342. http://dx.doi.org/10.3390/pr8111342.
Повний текст джерелаSaritha, Rajendhiran, Sesuraj Babiola Annes, Saravanan Subramanian, and Subburethinam Ramesh. "Correction: Carbazole based Electron Donor Acceptor (EDA) catalysis for the synthesis of biaryl and aryl–heteroaryl compounds." Organic & Biomolecular Chemistry 18, no. 15 (2020): 2962. http://dx.doi.org/10.1039/d0ob90043e.
Повний текст джерелаДисертації з теми "Aryls(Heteroaryls) compound"
Jha, Abadh Kishor. "New strategies towards the functionalization of C-H and C-Cl bond of Aryls(Heteroaryls) and synthesis of Aza-Heterocycles." Thesis, 2018. http://eprint.iitd.ac.in:80//handle/2074/7941.
Повний текст джерелаTseng, Tze-Wei, and 曾之緯. "Various and versatile methodologies for the preparation of aryl- and heteroaryl- fused coumarins, and their application to the synthesis of natural compounds: Angelicin, Seselin, Xanthxyletin and Psoralen." Thesis, 2011. http://ndltd.ncl.edu.tw/handle/07967068754465331747.
Повний текст джерела國立中正大學
化學研究所
99
Various synthetic methods of benzocoumarins are described in this study. In chapter 2, we have developed a new and useful method of preparing 5,6-benzocoumarins (2–2g) with different substituents on a variety of positions. Their molecular skeletons were formed from the oxidation of 2H-pyrans by DDQ reagent. These 2H-pyrans were prepared by tandem reaction of cis-hydrogenation of enynals and electrocyclization. Various α-tetralones were used as starting materials. Heteroarene-fused coumarins (2h–2k) were also prepared respectively. In chapter 3, a modified synthetic route – α-tetralone keto ester was catalyzed by DBU– for Michael addation is described. The results not only represent sizable yield of 7,8-benzocoumarins (3–3g, 22b, 22c, 26) under convenient conditions, but also provide an efficient route for the synthesis of some natural products, such as Angelicin (28), Seselin (33), and Pyrone (39, 39d). In chapter 4, a new benzocoumarin building block method from β-tetralone has been discovered, under the condition of propiolic acid and HOTf, to give Claisen rearrangement products. The 5,6-benzocoumarin carbon skeleton from substituted β-tetralone was built up in 2 steps. In final chapter, previous reaction condition was carried out naphthols and meta-substituted phenols. Aromatic coumarins (63–79) and some natural products (83, 87) were prepared respectively.
Частини книг з теми "Aryls(Heteroaryls) compound"
"2-Aryl(Heteroaryl)- and 2,3-Diaryl-(Diheteroaryl) Quinoxalines." In Chemistry of Heterocyclic Compounds: A Series Of Monographs, 233–40. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2008. http://dx.doi.org/10.1002/9780470187333.ch15.
Повний текст джерела