Synthetic Studies on Actinorhodin and γ-Actinorhodin: Synthesis of Deoxyactinorhodin and Deoxy-γ-actinorhodin/Crisamicin A Isomer
作者:Sandip V. Mulay、Rodney A. Fernandes
DOI:10.1002/chem.201406431
日期:2015.3.16
A strategy based on bidirectional Dötz benzannulation and the oxa‐Pictet–Spengler reaction toward the synthesis of actinorhodin and γ‐actinorhodin has been explored. This work has resulted in the synthesis of deoxyactinorhodin and deoxy‐γ‐actinorhodin. The latter is a regioisomer of crisamicin A (which has 10,10′‐dihydroxy groups).
探索了基于双向Dötz苯环和oxa-Pictet-Spengler反应合成放线菌丝蛋白和γ-放线菌丝蛋白的策略。这项工作导致了脱氧肌动蛋白原和脱氧-γ-肌动蛋白的合成。后者是crisamicin A的区域异构体(具有10,10'-二羟基)。