An approach to the C(17)–C(24) fragment of bryostatins: applications of stereoselective trisubstituted alkene formation by palladium(0) catalysed coupling of enol acetates and vinylic bromides
Author:
Publisher
Royal Society of Chemistry (RSC)
Link
http://pubs.rsc.org/en/content/articlepdf/1998/P1/A803425G
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. Synthetic approaches to the C11–C27 fragments of bryostatins;Organic & Biomolecular Chemistry;2017
2. Syntheses of C17–C27 fragments of 20-deoxybryostatins for assembly using Julia and metathesis reactions;Organic & Biomolecular Chemistry;2017
3. A Catalytic Intermolecular Formal Ene Reaction between Ketone-Derived Silyl Enol Ethers and Alkynes;Journal of the American Chemical Society;2016-09-16
4. Palladium- and Nickel-Catalyzed Alkenylation of Enolates;Chemistry - A European Journal;2013-01-16
5. ChemInform Abstract: An Approach to the C(17)-C(24) Fragment of Bryostatins: Applications of Stereoselective Trisubstituted Alkene Formation by Palladium(0) Catalyzed Coupling of Enol Acetates and Vinylic Bromides.;ChemInform;2010-06-18
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