Expedient Synthesis of Chiral Oxazolidinone Scaffolds via Rhodium-Catalyzed Asymmetric Ring-Opening with Sodium Cyanate
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https://figshare.com/articles/dataset/Expedient_Synthesis_of_Chiral_Oxazolidinone_Scaffolds_via_Rhodium_Catalyzed_Asymmetric_Ring_Opening_with_Sodium_Cyanate/2438860
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资源简介：
A method for synthesizing chiral oxazolidinone scaffolds from readily available oxabicyclic alkenes is described. The reaction utilizes a domino sequence of Rh(I)-catalyzed asymmetric ring-opening (ARO) with sodium cyanate as a novel nucleophile followed by intramolecular cyclization to generate oxazolidinone products in excellent enantioselectivities (trans stereochemistry).
创建时间：
2016-02-19
