Highly Stereoselective Synthesis of Fluoroalkene Dipeptides via the Novel Chromium(II)-Mediated Carbon–Fluorine Bond Cleavage/New Carbon–Carbon Bond Formation
Author:
Affiliation:
1. Faculty of Molecular Chemistry and Engineering, Kyoto Institute of Technology
2. Department of Chemistry Biology and Marine Science, University of the Ryukyus
Publisher
Georg Thieme Verlag KG
Subject
Organic Chemistry,Catalysis
Link
http://www.thieme-connect.de/products/ejournals/pdf/10.1055/s-0035-1560390.pdf
Cited by 12 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. Selective Synthesis of (Z)- and (E)-β-Fluoro-α,β-Unsaturated Amides Using Palladium-Catalyzed Aminocarbonylation;Organic Letters;2023-09-10
2. Palladium-catalyzed selective defluorinative arylation for the efficient stereospecific synthesis of (E)-β-fluoroacrylamides;Organic Chemistry Frontiers;2021
3. Gold-Catalyzed Addition–N-Boc Cleavage–Cyclization of N,O-Acetal with Ynamides for Construction of 6-(tert-Butyldimethylsilyl)oxy-tetrahydropyrrolo[1,2-c][1,3]oxazin-1-ones;The Journal of Organic Chemistry;2020-09-14
4. Synthesis of β-Fluoro-α,β-Unsaturated Amides from the Fragmentation of Morpholine 3,3,3-Trifluoropropanamide by Grignard Reagents;Organic Letters;2020-03-17
5. Reductive Bromodifluoromethylation of Nitrones Promoted by Visible Light;European Journal of Organic Chemistry;2019-04-01
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