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Refinado por: Nome da Publicação: Chemical Communications remover assunto: Stereoisomerism remover
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N and S co-doped porous carbon spheres prepared using L-cysteine as a dual functional agent for high-performance lithium-sulfur batteries
N and S co-doped porous carbon spheres prepared using L-cysteine as a dual functional agent for high-performance lithium-sulfur batteries
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N and S co-doped porous carbon spheres prepared using L-cysteine as a dual functional agent for high-performance lithium-sulfur batteries

Niu, Shuzhang ; Lv, Wei ; Zhou, Guangmin ; He, Yanbing ; Li, Baohua ; Yang, Quan-Hong ; Kang, Feiyu

Chemical communications (Cambridge, England), 2015-01, Vol.51 (100), p.17720-17723 [Periódico revisado por pares]

England

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2
MCF-supported boronic acids as efficient catalysts for direct amide condensation of carboxylic acids and amines
MCF-supported boronic acids as efficient catalysts for direct amide condensation of carboxylic acids and amines
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MCF-supported boronic acids as efficient catalysts for direct amide condensation of carboxylic acids and amines

Gu, Liuqun ; Lim, Jaehong ; Cheong, Jian Liang ; Lee, Su Seong

Chemical communications (Cambridge, England), 2014-01, Vol.50 (53), p.7017-7019 [Periódico revisado por pares]

England

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3
Use of a hydrogel polymer for reproducible surface enhanced Raman optical activity (SEROA)
Use of a hydrogel polymer for reproducible surface enhanced Raman optical activity (SEROA)
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Use of a hydrogel polymer for reproducible surface enhanced Raman optical activity (SEROA)

Pour, Saeideh Ostovar ; Bell, Steven E J ; Blanch, Ewan W

Chemical communications (Cambridge, England), 2011-04, Vol.47 (16), p.4754-4756 [Periódico revisado por pares]

England

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4
Molecular amplification of two different receptors using diastereomeric templates
Molecular amplification of two different receptors using diastereomeric templates
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Molecular amplification of two different receptors using diastereomeric templates

Bulos, Fernando ; Roberts, Sarah L ; Furlan, Ricardo L E ; Sanders, Jeremy K M

Chemical communications (Cambridge, England), 2007-01 (29), p.3092-3093 [Periódico revisado por pares]

England

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5
Light-controlled ion channels formed by amphiphilic small molecules regulate ion conduction via cis-trans photoisomerization
Light-controlled ion channels formed by amphiphilic small molecules regulate ion conduction via cis-trans photoisomerization
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Light-controlled ion channels formed by amphiphilic small molecules regulate ion conduction via cis-trans photoisomerization

Liu, Tao ; Bao, Chunyan ; Wang, Haiyan ; Lin, Yao ; Jia, Huijuan ; Zhu, Linyong

Chemical communications (Cambridge, England), 2013-01, Vol.49 (87), p.10311-10313 [Periódico revisado por pares]

England

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6
Surfactant-type asymmetric organocatalyst: organocatalytic asymmetric Michael addition to nitrostyrenes in water
Surfactant-type asymmetric organocatalyst: organocatalytic asymmetric Michael addition to nitrostyrenes in water
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Surfactant-type asymmetric organocatalyst: organocatalytic asymmetric Michael addition to nitrostyrenes in water

Luo, Sanzhong ; Mi, Xueling ; Liu, Song ; Xu, Hui ; Cheng, Jin-Pei

Chemical communications (Cambridge, England), 2006-01 (35), p.3687-3689 [Periódico revisado por pares]

England

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7
trans-2-Aminocyclohexanol as a pH-sensitive conformational switch in lipid amphiphiles
trans-2-Aminocyclohexanol as a pH-sensitive conformational switch in lipid amphiphiles
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trans-2-Aminocyclohexanol as a pH-sensitive conformational switch in lipid amphiphiles

Brazdova, Barbora ; Zhang, Ningrong ; Samoshin, Vyacheslav V ; Guo, Xin

Chemical communications (Cambridge, England), 2008-01 (39), p.4774-4776 [Periódico revisado por pares]

England

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8
Aqueous nanofibers with switchable chirality formed of self-assembled dumbbell-shaped rod amphiphiles
Aqueous nanofibers with switchable chirality formed of self-assembled dumbbell-shaped rod amphiphiles
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Aqueous nanofibers with switchable chirality formed of self-assembled dumbbell-shaped rod amphiphiles

Huang, Zhegang ; Lee, Eunji ; Kim, Ho-Joong ; Lee, Myongsoo

Chemical communications (Cambridge, England), 2009-01 (44), p.6819-6821 [Periódico revisado por pares]

England

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9
Monolayer lipid membrane-forming dissymmetrical bolaamphiphiles derived from alginate oligosaccharides
Monolayer lipid membrane-forming dissymmetrical bolaamphiphiles derived from alginate oligosaccharides
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Monolayer lipid membrane-forming dissymmetrical bolaamphiphiles derived from alginate oligosaccharides

Roussel, M ; Lognoné, V ; Plusquellec, D ; Benvegnu, T

Chemical communications (Cambridge, England), 2006-01, Vol.34 (34), p.3622-3624 [Periódico revisado por pares]

England: Royal Society of Chemistry

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10
Highly selective reduction of nitroarenes by iron(0) nanoparticles in water
Highly selective reduction of nitroarenes by iron(0) nanoparticles in water
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Highly selective reduction of nitroarenes by iron(0) nanoparticles in water

Dey, Raju ; Mukherjee, Nirmalya ; Ahammed, Sabir ; Ranu, Brindaban C

Chemical communications (Cambridge, England), 2012-01, Vol.48 (64), p.7982-7984 [Periódico revisado por pares]

England

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