Zobrazeno 1 - 10
of 62
pro vyhledávání: '"Zhangpei Chen"'
Publikováno v:
Water Science and Technology, Vol 86, Iss 3, Pp 496-510 (2022)
Microporous organic polymers (MOPs) possessing large specific surface area with high stability are suitable adsorbent to remove contaminants from water, such as organic pollutant and heavy metal contaminants. Herein, a phenanthroline-based microporou
Externí odkaz:
https://doaj.org/article/866bb11a859945e5a57fd701561646f5
Autor:
Dawei Cao, Mohamad Ataya, Zhangpei Chen, Huiying Zeng, Yong Peng, Rustam Z. Khaliullin, Chao-Jun Li
Publikováno v:
Nature Communications, Vol 13, Iss 1, Pp 1-8 (2022)
The cleavage and formation of carbon−carbon bonds is an important strategy for structural modifications in organic syntheses. Herein, the authors present a photoinduced method to construct biaryl compounds through dual inert C−C bond cleavage.
Externí odkaz:
https://doaj.org/article/7c9d7a1aa1884732be54e45ec9c0e80a
Publikováno v:
iScience, Vol 23, Iss 8, Pp 101419- (2020)
Summary: Hydroxyl is widely found in organic molecules as functional group and its deprivation plays an inevitable role in organic synthesis. However, the direct cleavage of Csp3-O bond in alcohols with high selectivity and efficiency, especially wit
Externí odkaz:
https://doaj.org/article/e5cd7dd4f05c4d0db1a650c3872ab12f
Publikováno v:
Molecules, Vol 23, Iss 6, p 1240 (2018)
An efficient and practical approach towards bifunctional phosphorus phenols has been developed through a reaction of diphenylphosphine oxide and the o-quinone methides in situ generated from 2-tosylalkyl phenols under basic conditions. This protocol
Externí odkaz:
https://doaj.org/article/b1a5360a02214051abf38a372d3d39cd
Autor:
Yujiao Xie, Xiaofeng Liu, Zhuang Hu, Zhipeng Hou, Zhihao Guo, Zhangpei Chen, Jianshe Hu, Liqun Yang
Publikováno v:
Nanomaterials, Vol 8, Iss 4, p 195 (2018)
New amphiphilic liquid crystal (LC) polycarbonate block copolymers containing side-chain cholesteryl units were synthesized. Their structure, thermal stability, and LC phase behavior were characterized with Fourier transform infrared (FT-IR) spectrum
Externí odkaz:
https://doaj.org/article/ed01b41cf9384098a7e51dfd4d5c5416
Publikováno v:
Polymers, Vol 9, Iss 11, p 605 (2017)
The in vitro enzymatic degradation of cross-linked poly(trimethylene carbonate) networks (PTMC-Ns) was performed in lipase solutions at 37 °C, and the effect of the initial molecular weight and cross-linker amount as well as the cross-linker type on
Externí odkaz:
https://doaj.org/article/4e3088a83d6e46d6979b0d09341caa57
Publikováno v:
Organic & Biomolecular Chemistry. 21:775-782
A rhodium-catalyzed formal [4 + 1]-cyclization reaction of aryl substituted pyrazoles with cyclopropanols via C–H bond activation/cyclization processes to selectively construct a series of carbonyl functionalized pyrazolo[5,1-a]isoindoles is descri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7cc9844b940a282284cb4a4e83ce29e3
https://doi.org/10.1039/d2ob02001g
https://doi.org/10.1039/d2ob02001g
Publikováno v:
New Journal of Chemistry. 47:297-306
CS/ZIF-8@COFa-4@Pd showed excellent activity in the Suzuki reaction and the reduction reaction of p-NP.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c6749620d8df21cc674184abbb558283
https://doi.org/10.1039/d2nj04884a
https://doi.org/10.1039/d2nj04884a
Autor:
Yan Mao, Wenxi Chen, Changchang Li, Lin Miao, Yanfei Lin, Fei Ling, Zhangpei Chen, Jinzhong Yao
Publikováno v:
Chemical Communications. 59:3775-3778
The efficient rhodium(iii)-catalyzed coupling of phosphonium cations with internal alkynes for the construction of various 3,4,5-trisubstituted phenols is described.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b42067609e94904db5c816091479a963
https://doi.org/10.1039/d3cc00017f
https://doi.org/10.1039/d3cc00017f
Publikováno v:
Journal of Catalysis. 416:29-38
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5e4d9421f13b59e487a014517ec034c9
https://doi.org/10.1016/j.jcat.2022.10.019
https://doi.org/10.1016/j.jcat.2022.10.019