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Collect. Czech. Chem. Commun. 1981, 46, 717-728
https://doi.org/10.1135/cccc19810717

Stereochemical course of the reaction of 2-haloethyl isothiocyanates with nucleophiles. Stereospecific route to 4,5-disubstituted Δ2-thiazolines and thiazolidine-2-thiones

Ladislav Kniežoa, Pavol Kristiana, Miloš Buděšínskýb and Katarína Havrilováa

a Department of Organic Chemistry, P. J. Šafárik University, 041 67 Košice
b Institute of Organic Chemistry and Biochemistry, Czechoslovak Academy of Sciences, 166 10 Prague 6

Crossref Cited-by Linking

  • Gao Simiao, Zhang Yu, Dong Jun, Chen Ning, Xu Jiaxi: Synthesis of functionalized 5-substituted thiazolidine-2-thiones via adscititious xanthate-promoted radical cyclization of allyl(alkyl/aryl)dithiocarbamates. Org. Biomol. Chem. 2016, 14, 1002. <https://doi.org/10.1039/C5OB02297E>
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  • Cutugno Sara, Martelli Gianluca, Negro Lucia, Savoia Diego: The Reaction of β-Amino Alcohols with 1,1′-Carbonyldiimidazole − Influence of the Nitrogen Substituent on the Reaction Course. Eur. J. Org. Chem. 2001, 2001, 517. <https://doi.org/10.1002/1099-0690(200102)2001:3<517::AID-EJOC517>3.0.CO;2-N>
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  • KNIEZO L., KRISTIAN P., BUDESINSKY M., HAVRILOVA K.: ChemInform Abstract: STEREOCHEMICAL COURSE OF THE REACTION OF 2‐HALOETHYL ISOTHIOCYANATES WITH NUCLEOPHILES. STEREOSPECIFIC ROUTE TO 4,5‐DISUBSTITUTED Δ2‐THIAZOLINES AND THIAZOLIDINE‐2‐THIONES. Chemischer Informationsdienst 1981, 12. <https://doi.org/10.1002/chin.198130223>