A Convenient Synthesis of N2-Alkylated Guanines


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Resumo

An improved three-step synthesis of N2-alkylated guanines has been developed starting from N2-Boc-protected 2-amino-6-chloropurine which was treated with Boc2O, and the resulting doubly N2,9-protected derivative was subjected to N2-alkylation with alkyl halides, followed by hydrolysis. The advantages of this procedure include short reaction steps, simple operations, and good yields.

Sobre autores

H. Zhu

Shanghai Engineering Research Center of Molecular Therapeutics and New Drug Development, School of Chemistry and Molecular Engineering

Email: yluo@chem.ecnu.edu.cn
República Popular da China, Shanghai

L. Qin

Shanghai Engineering Research Center of Molecular Therapeutics and New Drug Development, School of Chemistry and Molecular Engineering

Email: yluo@chem.ecnu.edu.cn
República Popular da China, Shanghai

T. Liu

Shanghai Engineering Research Center of Molecular Therapeutics and New Drug Development, School of Chemistry and Molecular Engineering

Email: yluo@chem.ecnu.edu.cn
República Popular da China, Shanghai

Y. Luo

Shanghai Engineering Research Center of Molecular Therapeutics and New Drug Development, School of Chemistry and Molecular Engineering

Autor responsável pela correspondência
Email: yluo@chem.ecnu.edu.cn
República Popular da China, Shanghai

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