In-Solution and On-Plate Light-Catalyzed E/Z Isomerization of Cyclic Chalcone Analogues. Lipophilicity of E- and Z-2-(X-Benzylidene)-1-Benzosuberones
Author:
Publisher
Oxford University Press (OUP)
Subject
General Medicine,Analytical Chemistry
Link
http://academic.oup.com/chromsci/article-pdf/43/6/289/1024290/43-6-289.pdf
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2. Synthesis and reactivity of α-sulfenyl-β-chloroenones, including oxidation and Stille cross-coupling to form chalcone derivatives;Tetrahedron;2021-05
3. Synthesis and biological evaluation of structurally diverse α-conformationally restricted chalcones and related analogues;MedChemComm;2019
4. (E)-2-Benzylidenebenzocyclanones: part XIII—(E)/(Z)-Isomerization of some cyclic chalcone analogues. Effect of ring size on lipophilicity of geometric isomers;Monatshefte für Chemie - Chemical Monthly;2015-04-09
5. Structures of the conformational isomers and polymorph modifications of N-substituted 2,6-(E,E)-bis(ferrocenylidene)piperid-4-ones: photo- and electrochemically induced E/Z isomerization;CrystEngComm;2015
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