Correction: Laser cleavable probes for in situ multiplexed glycan detection by single cell mass spectrometry
Literature Information
Xi Huang, Huihui Liu, Jiyun Wang, Caiqiao Xiong
Correction for ‘Laser cleavable probes for in situ multiplexed glycan detection by single cell mass spectrometry’ by Jing Han et al., Chem. Sci., 2019, 10, 10958–10962.
Related Literature
Synthesis of silica supported AuCu nanoparticlecatalysts and the effects of pretreatment conditions for the CO oxidation reaction
J. Chris Bauer, David Mullins, Meijun Li, E. Andrew Payzant
DOI: 10.1039/C0CP01859G
Determining excitation temperature of fragmented C60via momentum distributions of fragments
D. B. Qian, X. Ma, Z. Chen, X. L. Zhu, H. P. Liu
DOI: 10.1039/C0CP00773K
The role of hydrogen bonding in water–metal interactions
Adrien Poissier, Sriram Ganeshan, M. V. Fernández-Serra
DOI: 10.1039/C0CP00994F
Ion conducting particle networks in liquids: modeling of network percolation and stability
Anna Jarosik, Uwe Traub, Joachim Maier, Armin Bunde
DOI: 10.1039/C0CP01870H
Molecular organization of hydrophobic molecules and co-adsorbed water in SBA-15 ordered mesoporous silica material
Randy Mellaerts, Maarten B. J. Roeffaers, Kristof Houthoofd, Michiel Van Speybroeck, Gert De Cremer, Jasper A. G. Jammaer, Guy Van den Mooter, Patrick Augustijns, Johan Hofkens, Johan A. Martens
DOI: 10.1039/C0CP01640C
Growth kinetic of single and double-walled aluminogermanate imogolite-like nanotubes: an experimental and modeling approach
Perrine Maillet
DOI: 10.1039/C0CP01851A
Simple synthesis of Pd–Fe3O4 heterodimer nanocrystals and their application as a magnetically recyclable catalyst for Suzuki cross-coupling reactions
Youngjin Jang, Jooyoung Chung, Seyoung Kim, Samuel Woojoo Jun, Byung Hyo Kim, Dong Won Lee, B. Moon Kim, Taeghwan Hyeon
DOI: 10.1039/C0CP01680B
Low-temperature decomposition of methanol on Au nanoclusters supported on a thin film of Al2O3/NiAl(100)
Guo-Rue Hu, Chen-Sheng Chao, Hong-Wan Shiu, Cheng-Ting Wang, Won-Ru Lin, Yao-Jane Hsu, Meng-Fan Luo
DOI: 10.1039/C0CP00526F
You might also like
What are the main uses of 1H-Indazole-6-carbonitrile (CAS: 141290-59-7)?
1H-Indazole-6-carbonitrile finds applications in pharmaceuticals, where it serve...
How should waste containing Dioctyl (2E)-2-butenedioate (CAS: 2997-85-5) be handled?
Waste containing Dioctyl (2E)-2-butenedioate (CAS: 2997-85-5) should be collecte...
What industries use Sodium [(1,2-benzoxazol-3-ylmethyl)sulfonyl]azanide (CAS: 68291-98-5)?
Sodium [(1,2-benzoxazol-3-ylmethyl)sulfonyl]azanide is primarily used in pharmac...
Are there alternatives to Dimethyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2,6-pyridinedicarboxylate (CAS: 741709-66-0) in synthesis?
Dimethyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2,6-pyridinedicarboxyla...
How should waste containing 2-Fluoro-6-hydrazinopyridine (CAS: 80714-39-2) be handled?
Waste containing 2-Fluoro-6-hydrazinopyridine (CAS: 80714-39-2) should be manage...
What is 6-Formyl-2-pyridinecarboxylic acid (CAS: 499214-11-8)?
6-Formyl-2-pyridinecarboxylic acid is an organic compound with the molecular for...
What is the market or research trend for 3-(3,4-dimethoxyphenyl)-2,5-dimethyl-N-(2-morpholin-4-ylethyl)pyrazolo[1,5-a]pyrimidin-7-amine (CAS: 900874-91-1)?
Research trends for this compound indicate a focus on its potential applications...
How is 9H-Tribenzo[b,d,f]azepine (CAS: 29875-73-8) typically synthesized?
9H-Tribenzo[b,d,f]azepine is typically synthesized via a multi-step process invo...
How is 1-Cyclopropyl-7-ethoxy-6-fluoro-8-methoxy-4-oxo-1,4-dihydro-3-quinolinecarboxylic acid (CAS: 1797982-51-4) typically synthesized?
1-Cyclopropyl-7-ethoxy-6-fluoro-8-methoxy-4-oxo-1,4-dihydro-3-quinolinecarboxyli...
How should waste containing Methyl 3-oxo-1,2,3,4-tetrahydro-6-quinoxalinecarboxylate (CAS: 671820-52-3) be handled?
Waste containing Methyl 3-oxo-1,2,3,4-tetrahydro-6-quinoxalinecarboxylate (CAS: ...
Source Journal
Chemical Science

Our journal has a wide-ranging scope which covers the full breadth of the chemical sciences. The research we publish contains the sorts of novel ideas, challenging questions and progressive thinking that bring undiscovered breakthroughs within reach. Your paper could focus on a single area, or cross many. It could be beyond the accepted bounds of the chemical sciences. It might address an immediate challenge, contribute to a future breakthrough or be wholly conceptual. We’re a team from every field of the chemical sciences, and know from experience that breakthroughs that drive the solutions to global challenges can come from anywhere, at any time. You could even start an entirely new area of research. Too bold? Too progressive? No such thing














