Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Yun Cheuk Leung"'
Autor:
Raju Cheerlavancha, Ahmed Ahmed, Yun Cheuk Leung, Aggie Lawer, Qing-Quan Liu, Marina Cagnes, Hee-Chan Jang, Xiang-Guo Hu, Luke Hunter
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 13, Iss 1, Pp 2316-2325 (2017)
Backbone-extended amino acids have a variety of potential applications in peptide and protein science, particularly if the geometry of the amino acid is controllable. Here we describe the synthesis of δ-amino acids that contain three vicinal C–F b
Externí odkaz:
https://doaj.org/article/8f6f4ba5619d414e9591e238346ecde5
Autor:
Zhiyong Wang, Eddy Pasquier, Flora Mansour, Renate Griffith, Xiang-Guo Hu, Yun Cheuk Leung, Luke Hunter, Johny Trinh, Christina Gonzalez, Catherine Au
Publikováno v:
Organic and Biomolecular Chemistry
Organic and Biomolecular Chemistry, Royal Society of Chemistry, 2019, 17 (3), pp.664-674. ⟨10.1039/c8ob02679c⟩
Organic & Biomolecular Chemistry
Organic & Biomolecular Chemistry, 2019, 17 (3), pp.664-674. ⟨10.1039/c8ob02679c⟩
Organic and Biomolecular Chemistry, Royal Society of Chemistry, 2019, 17 (3), pp.664-674. ⟨10.1039/c8ob02679c⟩
Organic & Biomolecular Chemistry
Organic & Biomolecular Chemistry, 2019, 17 (3), pp.664-674. ⟨10.1039/c8ob02679c⟩
International audience; Stereoselective fluorination is investigated as a method for modulating the properties of a cyclic RGD-containing tetrapeptide. Three key outcomes of fluorination are assessed: (i) the effect on peptide cyclisation efficiency;
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f3b393b5a8b17f606106d8d1ed5ac912
https://hal.archives-ouvertes.fr/hal-02503849
https://hal.archives-ouvertes.fr/hal-02503849
Autor:
Mohan Bhadbade, Satyanarayana Gadde, Naresh Kumar, David StC. Black, Yun Cheuk Leung, Belamy B. Cheung
Publikováno v:
Australian Journal of Chemistry. 73:1208
The reactivity and synthesis of new analogues of pyrido[1,2-a]benzimidazoles have been explored. Twenty-three derivatives bearing phenoxy, thiophenoxy, aniline, and aryl groups at the 1-position were successfully synthesised in 25–91% yield, via nu