Crystal Structure of Two Dimethyl 1,3-Thiazolidinedicarboxylates Obtained in Thermal [2 + 3]Cycloaddition of an Azomethine Ylide with 2,2,4,4-Tetramethyl-3-Thioxocyclobutanone |
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Authors: | Ma?gorzata?Domaga?a mailto:reczek@uni.lodz.pl" title=" reczek@uni.lodz.pl" itemprop=" email" data-track=" click" data-track-action=" Email author" data-track-label=" " >Email author,Magdalena?Ma?ecka,Katarzyna?Urbaniak,Grzegorz?Mlostoń,S?awomir?J.?Grabowski |
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Affiliation: | (1) Department of Crystallography and Crystal Chemistry, University of ód , Pomorska 149/153, PL-90236 ód , Poland;(2) Section of Heteroorganic Compounds, University of ód , Narutowicza 68, PL-90136 ód , Poland |
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Abstract: | ![]() The crystal structures of dimethyl 2,2,4,4-tetramethyl-3-oxocyclobutane-1-spiro-5 -3 ,4 -diphenyl-(1,3)-thiazolidine-2 ,2 -dicarboxylate, C26H29NO5S for V, and dimethyl 3,4-diphenyl-5-isopropylidene-(1,3)-thiazolidine-2,2-dicarboxylate, C22H23NO4S for VI, have been solved. The 1,3-thiazolidine ring of compound V has got twisted conformation, while in compound VI this ring adopts envelope. In both structures short inter- and intramolecular contacts were found, which can be recognized as hydrogen bonds. |
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Keywords: | Crystal and molecular structure C– H /content/n455343261437752/xxlarge8901.gif" alt=" sdot" align=" BASELINE" BORDER=" 0" > /content/n455343261437752/xxlarge8901.gif" alt=" sdot" align=" BASELINE" BORDER=" 0" > /content/n455343261437752/xxlarge8901.gif" alt=" sdot" align=" BASELINE" BORDER=" 0" >S hydrogen bonds The Bader theory [2 + 3]cycloaddition |
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