| dc.contributor.author | Yalcin, Serife Pinar | |
| dc.contributor.author | Klip, Nalan Terzioglu | |
| dc.contributor.author | BÜYÜKGÜNGÖR, ORHAN | |
| dc.contributor.author | AKKURT, MEHMET | |
| dc.date.accessioned | 2021-03-04T19:38:10Z | |
| dc.date.available | 2021-03-04T19:38:10Z | |
| dc.identifier.citation | AKKURT M., Yalcin S. P. , Klip N. T. , BÜYÜKGÜNGÖR O., "rac-2-hydroxy-2,8-dimethyl-4-morpholinoethyl-1-thia-4-azaspiro[4.5]decan-3-one", ACTA CRYSTALLOGRAPHICA SECTION E-STRUCTURE REPORTS ONLINE, cilt.64, 2008 | |
| dc.identifier.issn | 1600-5368 | |
| dc.identifier.other | vv_1032021 | |
| dc.identifier.other | av_90b2f972-1983-4995-a805-2012831df0c2 | |
| dc.identifier.uri | http://hdl.handle.net/20.500.12627/97667 | |
| dc.identifier.uri | https://doi.org/10.1107/s1600536808022447 | |
| dc.description.abstract | The title compound, C(16)H(28)N(2)O(3)S, is dimerized by inversion symmetry-related intermolecular O-H center dot center dot center dot N hydrogen bonding, forming an R(2)(2)(16) motif. The dimers are also linked through intermolecular C-H center dot center dot center dot O hydrogen bonding. The compound is chiral with a stereogenic centre located in the thiazole ring, but in the crystal structure it forms a racemate. The thiazole ring has an envelope conformation, while the cyclohexane and morpholine rings adopt chair conformations. | |
| dc.language.iso | eng | |
| dc.subject | Sıvı Kristaller ve Sıvı Kristal Polimerler | |
| dc.subject | Temel Bilimler | |
| dc.subject | Fizikokimya | |
| dc.subject | Temel Bilimler (SCI) | |
| dc.subject | Kimya | |
| dc.subject | KRİSTALLOGRAFİ | |
| dc.title | rac-2-hydroxy-2,8-dimethyl-4-morpholinoethyl-1-thia-4-azaspiro[4.5]decan-3-one | |
| dc.type | Makale | |
| dc.relation.journal | ACTA CRYSTALLOGRAPHICA SECTION E-STRUCTURE REPORTS ONLINE | |
| dc.contributor.department | Erciyes Üniversitesi , Fen Fakültesi , Katıhal Fiziği | |
| dc.identifier.volume | 64 | |
| dc.contributor.firstauthorID | 189126 | |
