An Ireland−Claisen Approach to Lignans: Synthesis of the Putative Structure of 5-epi-Eupomatilone-6
Author:
Affiliation:
1. Department of Chemistry and Biochemistry, University of Arkansas, Fayetteville, Arkansas 72701
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo049817r
Reference35 articles.
Cited by 26 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. Synthesis of γ-Lactones via the Kowalski Homologation Reaction: Protecting-Group-Free Divergent Total Syntheses of Eupomatilones-2,5,6, and 3-epi-Eupomatilone-6;Organic Letters;2019-09-26
2. Formal synthesis of (+)-3-epi-eupomatilone-6 and the 3,5-bis-epimer;Organic & Biomolecular Chemistry;2014-07-10
3. Vinyl Epoxides in Organic Synthesis;Chemical Reviews;2014-04-29
4. Stereoselective Synthesis of Quaternary Carbons via the Dianionic Ireland–Claisen Rearrangement;Organic Letters;2014-04-15
5. Hybrid Gold/Chiral Brønsted Acid Relay Catalysis Allows an Enantioselective Synthesis of (−)-5-epi-Eupomatilone-6;The Journal of Organic Chemistry;2013-12-18
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