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Enantioselective Rh-Catalyzed Carboacylation of CN Bonds via C–C Activation of Benzocyclobutenones

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NIAID Data Ecosystem2026-03-09 收录
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https://figshare.com/articles/dataset/Enantioselective_Rh_Catalyzed_Carboacylation_of_C_N_Bonds_via_C_C_Activation_of_Benzocyclobutenones/2089117
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Herein we describe the first enantioselective Rh-catalyzed carboacylation of oximes (imines) via C–C activation. In this transformation, the benzocyclobutenone C1–C2 bond is selectively activated by a low valent rhodium catalyst and subsequently the resulting two Rh–C bonds add across a CN bond, which provides a unique approach to access chiral lactams. A range of polycyclic nitrogen-containing scaffolds were obtained in good yields with excellent enantioselectivity. Further derivatization of the lactam products led to a rapid entry to various novel fused heterocycles.
创建时间:
2016-02-12
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