Successive Michael reaction-sigmatropic rearrangement of polyquinones with silyl ketene acetals
Author:
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo00284a038
Cited by 21 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Enantioselective Total Syntheses of Preussomerins: Control of Spiroacetal Stereogenicity by Photochemical Reaction of a Naphthoquinone through 1,6‐Hydrogen Atom Transfer;Angewandte Chemie;2022-12-21
2. Enantioselective Total Syntheses of Preussomerins: Control of Spiroacetal Stereogenicity by Photochemical Reaction of a Naphthoquinone through 1,6‐Hydrogen Atom Transfer;Angewandte Chemie International Edition;2022-12-21
3. Diastereoselective syntheses of substituted cis-hydrindanones featuring sequential inter- and intramolecular Michael reactions;Tetrahedron;2016-06
4. Synthesis of γ-butenolides and α,β-unsaturated γ-butyrolactams by addition of vinylogous nucleophiles to Michael acceptors;Tetrahedron;2014-04
5. Vinylogous Mukaiyama-Michael Reactions between 2-Silyloxyfurans and Cyclic Enones or Unsaturated Oxo Esters;European Journal of Organic Chemistry;2010-08-24
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