Reactive and ‘clickable’ electrospun polymeric nanofibers
文献信息
Ozlem I. Kalaoglu-Altan
This mini-review summarizes various approaches that have been employed to obtain functional electrospun polymeric nanofibers. Examples from recent literature are used to highlight the design of reactive and ‘clickable’ nanofibers that can be rendered with functional attributes through efficient conjugation of various molecules and macromolecules. The key role of contemporary synthetic polymer chemistry in enabling the synthesis of various reactive polymers as precursors for such reactive and ‘clickable’ fibers is clearly evident. A few reports have also demonstrated that ‘click’ reaction based strategies can be utilized towards fabrication of robust crosslinked or porous nanofibers as well as their subsequent functionalization.
相关文献
The radical acylarylation of N-arylacrylamides with aliphatic aldehydes using the photolysis of hypervalent iodine(iii) reagents
Ryu Sakamoto, Naomichi Hirama
DOI: 10.1039/C8OB01420E
Multigram synthesis of an orthogonally-protected pentasaccharide for use as a glycan precursor in a Shigella flexneri 3a conjugate vaccine: application to a ready-for-conjugation decasaccharide
Johan Cornil, Zhaoyu Hu, Marion Bouchet, Laurence A. Mulard
DOI: 10.1039/D1QO00761K
Synthesis and biological evaluation of cyclic derivatives of combretastatin A-4 containing group 14 elements
Víctor Blasco, Juan Murga, Eva Falomir, Miguel Carda, Santiago Royo, Ana C. Cuñat, Juan F. Sanz-Cervera, J. Alberto Marco
DOI: 10.1039/C8OB01148F
Ru(ii)-Catalyzed C–H activation/annulation reactions of N-aryl-pyrazolidinones with sulfoxonium ylides: synthesis of cinnoline-fused pyrazolidinones
Hai-Shan Jin, Ya-Zhen Du, Qing-Yang Zhao, Li-Ming Zhao
DOI: 10.1039/D1QO01001H
Ruthenium-catalyzed synthesis of arylethyl 1,3,5-triazines from arylallyl alcohols and biguanides
Chen Zhang
DOI: 10.1039/C8OB01397G
Copper-catalyzed [1,3]-alkoxy rearrangement for the selective synthesis of polycyclic ortho-aminoarenol derivatives
Itaru Nakamura, Satoru Nozawa, Yasuhiro Ishida, Ichiro Muranushi, Alexandra Mayerweg, Masahiro Terada
DOI: 10.1039/D1QO01189H
Ligand-accelerated site-selective Csp2–H and Csp3–H alkynylations of alcohols via Pd(ii) catalysis
Aidong Huang, Yishen Han, Peiqing Wu, Yang Gao, Yanping Huo, Qian Chen, Xianwei Li
DOI: 10.1039/D1QO01095F
Modular synthesis of (E)-cinnamaldehydes directly from allylarenes via a metal-free DDQ-mediated oxidative process
Ting-Ting Xu, Tao-Shan Jiang, Xiao-Lan Han, Yuan-Hong Xu, Jin-Ping Qiao
DOI: 10.1039/C8OB01469H
Catalytic asymmetric dearomative [4 + 2] annulation of 2-nitrobenzofurans and 5H-thiazol-4-ones: stereoselective construction of dihydrobenzofuran-bridged polycyclic skeletons
Jian-Qiang Zhao, Zhen-Hua Wang, Yong You, Shuang Chen, Xiong-Li Liu, Ming-Qiang Zhou, Wei-Cheng Yuan
DOI: 10.1039/D1QO01061A
Base controlled diverse reactivity of allyl cyanide for synthesis of multi-substituted benzenes
Pratik Yadav, Ranjay Shaw, Amr Elagamy, Abhinav Kumar, Ramendra Pratap
DOI: 10.1039/C8OB01270A
您可能还喜欢
如何储存1,2-环己二酮环乙缩醛(CAS号:4746-96-7)?
1,2-环己二酮环乙缩醛应储存在阴凉、干燥、通风良好的地方,避免阳光直射。建议使用密封容器保存,并保持环境温度在室温范围内,远离火源和热源。
Ecopladib(CAS号:381683-92-7)的市场或研究趋势如何?
Ecopladib作为一种新型的药物,主要应用于治疗高胆固醇等疾病。目前,市场和研究趋势显示,Ecopladib因其独特的药理作用而受到关注。随着对心血管疾病治...
2,3-Dimethyl-3H-imidazo[4,5-c]pyridine(CAS号:52538-09-7)通常如何合成?
2,3-二甲基-3H-咪唑[4,5-c]吡啶通常通过咪唑和2,3-二甲基吡啶的缩合反应合成。具体来说,将咪唑和2,3-二甲基吡啶在适当的溶剂中进行加热或加压反应...
2,3,4,5-tetrahydro-1H-3-苯并氮杂环;盐酸盐(CAS号:17379-01-0)的市场或研究趋势如何?
该化合物在药物化学和有机合成中有一定的应用。近年来,随着对新型药物化合物的需求增加,该化合物的研究趋势主要集中在探索其生物活性,尤其是其在神经系统疾病治疗中的潜...
如何储存盐酸甘氨酸丁酯(CAS号:13048-99-2)?
盐酸甘氨酸丁酯应储存在阴凉、干燥、通风良好的地方,避免阳光直射和高温环境,温度应控制在25℃以下。储存容器应密封,避免与空气中的水分和酸性物质接触,以防发生水解...
什么是2-Iodo-N,N-dimethylbenzamide(CAS号:54616-46-5)?
2-碘-N,N-二甲基苯胺是一种有机化合物,化学名为2-Iodo-N,N-dimethylbenzamide。其分子式为C<sub>9</sub>H<sub>1...
5-溴-2-(4H-1,2,4-三唑-4-基)吡啶(CAS号:959240-99-4)的市场或研究趋势如何?
随着医药、农药和新材料领域的发展,该化合物作为关键中间体的应用日益增多。特别是在药物合成中,由于其独特的化学性质,可以用于合成多种药物分子。未来的研究趋势可能集...
2,4-二溴-6-三氟甲基嘧啶(CAS号:785778-00-9)通常如何合成?
2,4-二溴-6-三氟甲基嘧啶通常通过溴化反应合成。首先,将6-三氟甲基嘧啶与溴化剂(如液溴)在适当的溶剂(如二氯甲烷、四氢呋喃)中反应,加入适当的催化剂(如四...
来源期刊
Polymer Chemistry

Polymer Chemistry welcomes submissions in all areas of polymer science that have a strong focus on macromolecular chemistry. Manuscripts may cover a broad range of fields, yet no direct application focus is required.












phosphoryl}methyl 4-methylbenzenesulfonate structure {[3-(Hexadecyloxy)propoxy](hydroxy)phosphoryl}methyl 4-methylbenzenesulfonate structure](https://cnstatic.chemtradehub.com/structs/864/864068-45-1-ba7c.webp)

