Clicking cyclophane to boron doped diamond surfaces
Author:
Publisher
Springer Science and Business Media LLC
Subject
Multidisciplinary
Link
http://link.springer.com/content/pdf/10.1007/s11434-013-5703-8
Reference22 articles.
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2. Tornoe C V, Christensen C, Meldal M. Peptidotriazoles on solid phase: [1,2,3]-triazoles by regiospecific copper (I)-catalyzed 1,3-dipolar cycloadditions of terminal alkynes to azides. J Org Chem, 2002, 67: 3057–3064
3. Kolb H C, Sharpless K B. The growing impact of click chemistry on drug discovery. Drug Disc Today, 2003, 8: 1128–1137
4. Binder W H, Sachsenhofer R. “Click” chemistry in polymer and materials science. Rapid Commun, 2007, 28: 15–54
5. Lutz J F. 1, 3-Dipolar cycloadditions of azides and alkynes: A universal ligation tool in polymer and materials science. Angew Chem Int Ed, 2007, 46: 1018–1025
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1. A facile and efficient route to one-pot synthesis of new cyclophanes using vinamidinium salts;RSC Advances;2021
2. Selected synthetic strategies to cyclophanes;Beilstein Journal of Organic Chemistry;2015-07-29
3. The XRD Patterns Analysis of Diamond/Porous Composite Membrane Deposited by Bias Voltage Assisted HFCVD;Applied Mechanics and Materials;2014-02-06
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