Zobrazeno 1 - 10
of 3 534
pro vyhledávání: '"suzuki coupling"'
Autor:
Ashok Raj Patel, Gurupada Maity, Tanmay K. Pati, Laksmikanta Adak, Christopher L. Cioffi, Subhash Banerjee
Publikováno v:
Frontiers in Chemistry, Vol 12 (2024)
We report the fabrication of a novel spinel-type Pd₀.₁Cu₀.₉Co₂O₄ nano-flake material designed for Mizoroki-Heck and Suzuki coupling-cum-transesterification reactions. The Pd₀.₁Cu₀.₉Co₂O₄ material was synthesized using a simple
Externí odkaz:
https://doaj.org/article/955a855e89374127891fab3205821096
Publikováno v:
Results in Chemistry, Vol 13, Iss , Pp 101938- (2025)
A new series of aryl derivatives of 4-(1H-imidazol-2-yl)-2-(pyrimidin-5-yl)oxazoles 11a–j were synthesised and their structures were characterized by analytical techniques. Further, the biological applications of the newly prepared compounds 11a–
Externí odkaz:
https://doaj.org/article/ff88c993a9ef458cb9b6c2def1b29652
Autor:
Muthipeedika Nibin Joy, Igor S. Kovalev, Olga V. Shabunina, Sougata Santra, Grigory V. Zyryanov
Publikováno v:
Antioxidants, Vol 13, Iss 10, p 1198 (2024)
A series of 16 (hetero)aryl compounds based on coumarin and equol has been efficiently synthesized by exploring the palladium-catalyzed Suzuki cross-coupling reactions. Polyphenol based on coumarin (4-methyl-7-hydroxy coumarin) was initially converte
Externí odkaz:
https://doaj.org/article/f142c9afebab48b1be9ed706aa61a732
Autor:
Jeannes Angelia, Leah Duong, Faye Yun, Anesa Mesic, Cassandra Yuan, Daniel Carr, Siena Gunari, Paula K. Hudson, Christophe Morisseau, Bruce D. Hammock, Ram Kandasamy, Stevan Pecic
Publikováno v:
Heliyon, Vol 10, Iss 11, Pp e32262- (2024)
Simultaneous inhibition of soluble epoxide hydrolase (sEH) and fatty acid amide hydrolase (FAAH) with a single small molecule represents a novel therapeutic approach in treating inflammatory pain, since both targets are involved in pain and inflammat
Externí odkaz:
https://doaj.org/article/a9debe63a822457898455455adf78d0e
Autor:
V. Parashuram, K. Aruna Kumari, Sai Charitha Mullaguri, Rama Krishna Kancha, Vasantha Mittapelli
Publikováno v:
Results in Chemistry, Vol 8, Iss , Pp 101554- (2024)
Substituted tetrahydropyrido[3,4-d]pyrimidine derivatives (2a-l) have been synthesized through a series of N-substitution, Suzuki coupling, deprotection and condensation reactions. The structure of new compounds was analysed by interpretations of FTI
Externí odkaz:
https://doaj.org/article/bcc18ce10ffd438eac272216c54e7194
Autor:
Lisha K. Poonacha, Rashmi Ramesh, Akshay Ravish, Arunkumar Mohan, Pradeep M. Uppar, Prashant K. Metri, Nanjunda Swamy Shivananju, Santosh L. Gaonkar, Shubha Gopal, Alexey Yu Sukhorukov, Vijay Pandey, Priya Babu Shubha, Basappa Basappa
Publikováno v:
Applied Microbiology, Vol 3, Iss 4, Pp 1214-1228 (2023)
Heterocyclic compounds can specifically regulate bacterial development by targeting specific bacterial enzymes and metabolic pathways. The ESKAPE pathogens are multidrug-resistant and cause nosocomial infections, which is one of the greatest challeng
Externí odkaz:
https://doaj.org/article/9b33de861b99471ab32c0f9333821a16
Autor:
Julia Senkina, Spencer Knapp
Publikováno v:
Molecules, Vol 29, Iss 15, p 3615 (2024)
In order to improve the drug-likeness qualities, the antimalarial endochin-like quinolone (ELQ) scaffold has been modified by replacing the 4-(trifluoromethoxy)phenyl portion with an isoidide unit that is further adjustable by varying the distal O-su
Externí odkaz:
https://doaj.org/article/00edeaaf174f47b69c73daba9889d46e
Autor:
Yingchun Wang, Tomas Opsomer, Flip de Jong, Davy Verhaeghe, Maarten Mulier, Luc Van Meervelt, Mark Van der Auweraer, Wim Dehaen
Publikováno v:
Molecules, Vol 29, Iss 10, p 2229 (2024)
Methyl 4-(1,3a,6a-triazapentalen-3-yl)benzoate (TAP1) shows interesting properties as a small molecule fluorophore. In the search for post-functionalization methods, palladium-catalyzed arylation reactions were demonstrated. Direct CH arylation react
Externí odkaz:
https://doaj.org/article/54ef184dae4c493fa0c0fe899979f3f2
Publikováno v:
Molecules, Vol 29, Iss 9, p 2126 (2024)
In this study, a library of 3,7-di(hetero)aryl-substituted 10-(3-trimethylammoniumpropyl)10H-phenothiazine salts is prepared. These title compounds and their precursors are reversible redox systems with tunable potentials. The Hammett correlation giv
Externí odkaz:
https://doaj.org/article/f0bccf511c164519a6e2abc67fb96290
Autor:
Hossam Nada, Ahmed Elkamhawy, Magda H. Abdellattif, Andrea Angeli, Chang Hoon Lee, Claudiu T. Supuran, Kyeong Lee
Publikováno v:
Journal of Enzyme Inhibition and Medicinal Chemistry, Vol 37, Iss 1, Pp 994-1004 (2022)
Human carbonic anhydrase inhibitors (hCAIs) are a key therapeutic class with a multitude of novel applications such as anticonvulsants, topically acting antiglaucoma, and anticancer drugs. Herein, a new series of 4-anilinoquinazoline-based benzenesul
Externí odkaz:
https://doaj.org/article/23a2051a84c34794a63961386609c546