Zobrazeno 1 - 10
of 127
pro vyhledávání: '"Jun-Li Hou"'
Autor:
Heng Wang, Xiaomin Qian, Kun Wang, Ma Su, Wei-Wei Haoyang, Xin Jiang, Robert Brzozowski, Ming Wang, Xiang Gao, Yiming Li, Bingqian Xu, Prahathees Eswara, Xin-Qi Hao, Weitao Gong, Jun-Li Hou, Jianfeng Cai, Xiaopeng Li
Publikováno v:
Nature Communications, Vol 9, Iss 1, Pp 1-9 (2018)
Nested structures are common throughout nature and art, yet remain challenging synthetic targets in supramolecular chemistry. Here, the authors design multitopic terpyridine ligands that coordinate into nested concentric hexagons, and show that these
Externí odkaz:
https://doaj.org/article/33c2acdae7c24c519611bd100bbe4abe
Publikováno v:
CCS Chemistry. :1-17
Publikováno v:
Journal of the American Chemical Society. 144:22858-22864
We report herein an efficient approach for the enantioselective synthesis of inherently chiral calix[4]arenes via palladium-catalyzed asymmetric intramolecular C-H arylations. Using a chiral bifunctional phosphine-carboxylate ligand, the inherent chi
Publikováno v:
Chinese Journal of Chemistry.
Publikováno v:
Chinese Journal of Chemistry. 40:1293-1297
Autor:
Jian-Da Sun, Qian Li, Wei-Wei Haoyang, Dan-Wei Zhang, Hui Wang, Wei Zhou, Da Ma, Jun-Li Hou, Zhan-Ting Li
Publikováno v:
Molecular Pharmaceutics. 19:953-962
Bacterial lipopolysaccharides (LPS, endotoxins) cause sepsis that is responsible for a huge amount of mortality globally. However, their neutralization or detoxification remains an unmet medical need. We envisaged that cationic organic frameworks wit
Publikováno v:
Nano Letters. 21:10494-10500
Anti-Aβ therapy has dominated clinical trials for the prevention and treatment of Alzheimer's disease (AD). However, suppressing Aβ aggregation and disintegrating mature fibrils simultaneously remains a great challenge. In this work, we developed a
Publikováno v:
Chinese Chemical Letters. :108566
Autor:
Zhan-Ting Li, Jun-Li Hou, Yunxiang Zhang, Yong-Hong Fu, Wenning Wang, Ya-Wei Li, Rongrong Wen, Maohua Yang, Zhao-Jun Yan
Publikováno v:
Journal of the American Chemical Society. 143:11332-11336
We developed a voltage-sensitive artificial transmembrane channel by mimicking the dipolar structure of natural alamethicin channel. The artificial channel featured a zwitterionic structure and could undergo voltage-driven flipping in the lipid bilay
Publikováno v:
Chemical Communications. 57:863-866
A series of peptide-appended bisresorcinarenes were synthesized, which adopted tubular conformation induced by intramolecular hydrogen bonds. The derivatives formed unimolecular artificial transmembrane channels in lipid bilayers to enable selective