Bi(OTf)3‑Catalyzed Tandem Meyer–Schuster Rearrangement and 1,4-Addition to the Resulting Vinyl Ketone
收藏Figshare2016-02-16 更新2026-04-29 收录
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https://figshare.com/articles/dataset/Bi_OTf_sub_3_sub_Catalyzed_Tandem_Meyer_Schuster_Rearrangement_and_1_4_Addition_to_the_Resulting_Vinyl_Ketone/2243980
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资源简介:
Bi(OTf)3-catalyzed Meyer–Schuster rearrangement of electron-rich propargyl alcohols, followed by 1,4-addition of the resulting vinyl ketone, proceeded smoothly though Meyer–Schuster rearrangement of primary propargyl alcohols is rare. This tandem reaction can be extended to an intramolecular version, featuring a one-pot dihydroquinolone synthesis.
创建时间:
2016-02-16



