期刊
CHEMICAL COMMUNICATIONS
卷 -, 期 11, 页码 1306-1307出版社
ROYAL SOC CHEMISTRY
DOI: 10.1039/b301726p
关键词
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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.
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