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Synthesis of novel 2‐amino‐6,8‐dithioxopurine derivatives
Author(s) -
Ikaunieks Martins,
Belyakov Sergey,
Madre Marina
Publication year - 2006
Publication title -
journal of heterocyclic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.321
H-Index - 59
eISSN - 1943-5193
pISSN - 0022-152X
DOI - 10.1002/jhet.5570430420
Subject(s) - chemistry , alkylation , purine , sulfur , stereochemistry , combinatorial chemistry , organic chemistry , catalysis , enzyme
The synthesis of novel 2‐amino‐9‐alkoxyalkylpurine derivatives with both identical and different sulfur containing substituents at positions 6 and 8 of the purine cycle has been accomplished. The thionation and alkylation of the key intermediate ‐ 2‐[2‐(acetylamino)‐6,8‐dichloro‐9 H ‐purin‐9‐yl]methoxyethyl acetate or its reactions with thiolates were used. The structures of compounds obtained were confirmed by spectroscopic data and X‐ray diffraction analysis.

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