Homochiral Recognition in the Crystals of Cyclic Sulfinamides: from the 1D Level to the 3D Level
Author:
Publisher
Pleiades Publishing Ltd
Subject
Materials Chemistry,Inorganic Chemistry,Physical and Theoretical Chemistry
Link
https://link.springer.com/content/pdf/10.1134/S0022476623080152.pdf
Reference27 articles.
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2. O. A. Lodochnikova, A. R. Zaripova, R. R. Fayzullin, A. I. Samigullina, I. I. Vandyukova, L. N. Potapova, and A. R. Kurbangalieva. “Doubly enantiophobic” behavior during crystallization of racemic 1,5-dihydro-2H-pyrrol-2-one thioether. CrystEngComm, 2018, 20(23), 3218-3227. https://doi.org/10.1039/c8ce00369f
3. D. P. Gerasimova, A. F. Saifina, D. V. Zakharychev, R. R. Fayzullin, A. R. Kurbangalieva, and O. A. Lodochnikova. The second example of doubly enantiophobic behavior during crystallization: a detailed crystallographic, thermochemical and spectroscopic study. CrystEngComm, 2021, 23(21), 3907-3918. https://doi.org/10.1039/d1ce00227a
4. D. P. Gerasimova, D. V. Zakharychev, A. F. Saifina, R. R. Fayzullin, A. R. Kurbangalieva, and O. A. Lodochnikova. Homochiral versus heterochiral crystallization of 3-pyrrolin-2-one thioether results in the score 2:1 in favor of homochirality. Cryst. Growth Des., 2022, 22(12), 7273-7284. https://doi.org/10.1021/acs.cgd.2c00916
5. O. A. Lodochnikova, L. T. Hoang, A. R. Zaripova, A. R. Kayumov, I. A. Litvinov, and A. R. Kurbangalieva. Cocrystallization of diastereomers in the series of 2(5H)-furanone bis-thioethers based on 1,2-phenylenedimethanethiol. Russ. Chem. Bull., 2016, 65(11), 2672-2677. https://doi.org/10.1007/s11172-016-1634-2
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