Recent Advances in Asymmetric [3,3]-Sigmatropic Rearrangements
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Synthesis 2003, No. 7, Print: 20 05 2003. Art Id.1437-210X,E;2003,0,07,0961,1008,ftx,en;E08002SS.pdf. © Georg Thieme Verlag Stuttgart · New York Abstract: The synthesis of new complex structures is still a challenge in preparative organic chemistry. Focusing on the generation of defined stereogenic centers, the [3,3]-sigmatropic rearrangements are known as reliable reactions. Always, a highly ordered transition state must be passed through, which allows the shift of chiral information from the reactant into the nascent product. Generally, the complete [1,3]and, frequently, the [1,4]-chirality transfer enables one to predict the configuration of the new centers.
منابع مشابه
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The Ireland-Claisen [3,3]-sigmatropic rearrangement has been used to access biologically important β,β'-dihydroxy α-amino acids. The rearrangement reported is highly stereoselective and offers excellent levels of remote stereocontrol. This strategy has been used to synthesize the natural immunosuppressant mycestericin G and ent-mycestericin G, allowing for a revision of absolute configuration o...
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تاریخ انتشار 2003