期刊
ORGANIC LETTERS
卷 8, 期 11, 页码 2293-2295出版社
AMER CHEMICAL SOC
DOI: 10.1021/ol060559p
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资金
- NIGMS NIH HHS [GM 65460] Funding Source: Medline
A synthetic route for obtaining functional group diversity in macromolecules is described. The route relies on the differential reactivity of substituted dichlorotriazines. Treatment of a triamine core with substituted dichlorotriazines cleanly yields tris(monochlorotriazines). Subsequent SNAr reactions with amine nucleophiles bearing the functional group of interest yield diversity. If the substituent on the dichlorotriazine is a protected nucleophile, deprotection of the functionalized core allows for iterative reactions and the synthesis of star, dendritic, and hybrid macromolecules.
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