A Convenient Synthesis of N2-Alkylated Guanines


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Аннотация

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.

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Авторлар туралы

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
ҚХР, 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
ҚХР, 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
ҚХР, Shanghai

Y. Luo

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

Хат алмасуға жауапты Автор.
Email: yluo@chem.ecnu.edu.cn
ҚХР, Shanghai

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