Abstract
Diversity-oriented synthesis (DOS) has been widely applied in the generation of a large collection of highly functionalized molecules with diverse chemical skeletons. Herein, we report the diversity-oriented synthesis of a series of structurally diverse bicyclic substrates via an efficient tandem conjugate addition/aldol process followed by ring-closing metathesis (RCM). This approach allows us to efficiently prepare a number of structurally complex molecules for the further chemical biology studies.
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Li, C., Li, X., Wang, X. et al. Diversity-oriented synthesis of bicyclic ring systems via a conjugate addition/aldol/RCM process. Sci. China Chem. 56, 337–341 (2013). https://doi.org/10.1007/s11426-012-4805-5
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DOI: https://doi.org/10.1007/s11426-012-4805-5