Abstract
A template–switching strategy based on the modularity of template-directed solid-state synthesis has been successfully utilised to achieve a quantitative, stereospecific solid-state synthesis of a p-[2.2]-cyclophane target in gram quantities. © 2003 The Royal Society of Chemistry.
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CITATION STYLE
APA
Friščič, T., & MacGillivray, L. R. (2003). ‘Template-switching’: a supramolecular strategy for the quantitative, gram-scale construction of a molecular target in the solid state. Chemical Communications, 3(11), 1306–1307. https://doi.org/10.1039/b301726p
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