作者: Nathanael S. Gray , Qiang Ding , Peter G. Schultz , Sheng Ding
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摘要: The invention provides general methods for preparing 2,9-, 2,6,9-, O6-aryl- and O6-alkyl-substituted purines in a combinatorial traceless fashion. involve, some embodiments, Mitsunobu alkylation of 2-fluoro-6-phenylsulfenylpurine at N9 with alcohols solution, followed by C2-capture the purine core resin-bound amine subsequent oxidation displacement C6 sulfonyl group amines anilines.