首页 | 本学科首页   官方微博 | 高级检索  
     


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
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
Affiliation:(1) Department of Crystallography and Crystal Chemistry, University of "lstrok"ód"zacute", Pomorska 149/153, PL-90236 "lstrok"ód"zacute", Poland;(2) Section of Heteroorganic Compounds, University of "lstrok"ód"zacute", Narutowicza 68, PL-90136 "lstrok"ód"zacute", Poland
Abstract:
The crystal structures of dimethyl 2,2,4,4-tetramethyl-3-oxocyclobutane-1-spiro-5prime-3prime,4prime-diphenyl-(1,3)-thiazolidine-2prime,2prime-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.
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
本文献已被 SpringerLink 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号