Zobrazeno 1 - 10
of 54
pro vyhledávání: '"ZHAO LI"'
Publikováno v:
J Am Chem Soc
Self-assembly of amphiphilic peptide-based building blocks gives rise to a plethora of interesting nanostructures such as ribbons, fibers, and tubes. However, it remains a great challenge to employ peptide self-assembly to directly produce nanostruct
Publikováno v:
The Journal of Organic Chemistry. 85:9844-9849
A C-terminal amidothiourea motif is shown to promote a β-turn-like folded conformation in a series of β-amino acid-based short peptides in both the solid state and solution phase by an intramolecular 11-membered ring hydrogen bond.
Publikováno v:
Organic & Biomolecular Chemistry. 18:4590-4598
Proline based receptors (1-14) attached with phenylboronic acid and benzaldehyde binding groups at the N-/C- or C-/N-termini of the proline residue were created for chiral recognition of l-/d-DOPA, in an attempt to examine if balancing the two bindin
Autor:
Zhihan Zhang, Yongsheng Hou, Jinhong Chen, Yuqing Wang, Weiwei Gao, Tao Shi, Gao-Feng Yin, Fei Cao, Zhen Wang, Zhao Li, Xiaodong Wang
Publikováno v:
Organic letters. 23(16)
The proposed structures of parvistemoamide have been achieved by macrolactamization, but none of the characterization data of synthetic samples matched with those of the natural sample. The transformation of the highly strained 10-membered lactam rin
Autor:
Yuan Yuan, Jianbin Lin, Yun-Bao Jiang, Huan Luo, Yu-Wei Xiao, Si-Xian Wu, Zhao Li, Xiao-Sheng Yan
Publikováno v:
Chemical Communications. 55:12849-12852
We report coordination polymers forming from Ag+ and a chiral thiol ligand that bears a β-turn structure, exhibiting supramolecular chirality showing both the majority rules effect (MRE) and the racemate rules effect (RRE).
Autor:
Jinlian Cao, Shu-Ying Zhang, Tony D. James, Xiao-Sheng Yan, Miao Zhang, Zhao Li, Lin-E Guo, Yuan Hong, Yun-Bao Jiang
Publikováno v:
Guo, L-E, Hong, Y, Zhang, S-Y, Zhang, M, Yan, X-S, Cao, J-L, Li, Z, James, T D & Jiang, Y-B 2018, ' Proline-Based Boronic Acid Receptors for Chiral Recognition of Glucose ', Journal of Organic Chemistry, vol. 83, no. 24, pp. 15128-15135 . https://doi.org/10.1021/acs.joc.8b02425
Chiral recognition remains a major challenge in the area of molecular receptor design. With this research, we set out to explore the use of proline-based receptors for chiral recognition. Importantly, the proline structure allows for the introduction
Autor:
Li Li, Charles L. Liotta, Kristin R. McKenna, Pamela Pollet, Zhao Li, Ramanarayanan Krishnamurthy, Merranda Schmidt, Facundo M. Fernández, Leslie T. Gelbaum
Publikováno v:
Origins of life and evolution of the biosphere : the journal of the International Society for the Study of the Origin of Life. 49(4)
The prebiotic origin of polysaccharides, the largest class of biopolymers by mass in extant biology, has seldom been investigated experimentally. Herein, we report on the acid-catalyzed condensation of aqueous solutions of glucose, a model monosaccha
Publikováno v:
Medicinal Chemistry Research. 26:2538-2546
4-aminoacridone was efficiently synthesized using an optimized method and condensed with a variety of different aldehydes to give the corresponding Schiff bases, 1a–k. The antiproliferative activities of these compounds were measured against severa
Autor:
Wenzhong Huang, Xiangguang Li, Zhao Li, Hai Wang, Deqiang Liang, Baoling Wang, Yinhai Ma, Hongfu Zhou
Publikováno v:
Tetrahedron. 72:8442-8448
A novel and simple strategy for the visible light-induced efficient synthesis of indol-3-yl aryl ketones from readily available arylsulfonyl chlorides and indoles with CO at room temperature was developed. This metal-free protocol has good functional
Publikováno v:
ChemPlusChem. 81:1326-1332
Reported here is the induced helical aggregation of an achiral cationic perylene-3,4-dicarboximide (1) that contains a phenylboronic acid group, together with UMP that bears a cis-diol moiety able to interact with boronic acid and an imide group know