Highly Stereoselective C–C Bond Formation by Rhodium-Catalyzed Tandem Ylide Formation/[2,3]-Sigmatropic Rearrangement between Donor/Acceptor Carbenoids and Chiral Allylic Alcohols
收藏Figshare2016-02-20 更新2026-04-29 收录
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https://figshare.com/articles/dataset/Highly_Stereoselective_C_C_Bond_Formation_by_Rhodium_Catalyzed_Tandem_Ylide_Formation_2_3_Sigmatropic_Rearrangement_between_Donor_Acceptor_Carbenoids_and_Chiral_Allylic_Alcohols/2508367
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The tandem ylide formation/[2,3]-sigmatropic rearrangement between donor/acceptor rhodium carbenoids and chiral allyl alcohols is a convergent C–C bond forming process, which generates two vicinal stereogenic centers. Any of the four possible stereoisomers can be selectively synthesized by appropriate combination of the chiral catalyst Rh2(DOSP)4 and the chiral alcohol.
创建时间：
2016-02-20
