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dc.contributor.authorTong, Guanghu
dc.contributor.authorZhu, Bo
dc.contributor.authorLee, Richmond
dc.contributor.authorYang, Wenguo
dc.contributor.authorTan, Davin
dc.contributor.authorYang, Caiyun
dc.contributor.authorHan, Zhiqiang
dc.contributor.authorYan, Lin
dc.contributor.authorHuang, Kuo-Wei
dc.contributor.authorJiang, Zhiyong
dc.date.accessioned2017-06-06T08:33:42Z
dc.date.available2017-06-06T08:33:42Z
dc.date.issued2014-03-28
dc.identifier.citationTong, G., Zhu, B., Lee, R., Yang, W., Tan, D., Yang, C., … Jiang, Z. (2013). CCDC 909467: Experimental Crystal Structure Determination [Data set]. Cambridge Crystallographic Data Centre. https://doi.org/10.5517/cczjcnh
dc.identifier.doi10.5517/cczjcnh
dc.identifier.urihttp://hdl.handle.net/10754/624757
dc.description.abstractAn entry from the Cambridge Structural Database, the world’s repository for small molecule crystal structures. The entry contains experimental data from a crystal diffraction study. The deposited dataset for this entry is freely available from the CCDC and typically includes 3D coordinates, cell parameters, space group, experimental conditions and quality measures.
dc.formatCIF
dc.language.isoeng
dc.publisherCambridge Crystallographic Data Centre
dc.subjectCrystal Structure
dc.subjectExperimental 3D Coordinates
dc.subjectCrystal System
dc.subjectSpace Group
dc.subjectCell Parameters
dc.subjectCrystallography
dc.subjectMethyl 2-methylene-3-phenyl-4-(2-thienylcarbonyl)hex-5-enoate
dc.titleCCDC 909467: Experimental Crystal Structure Determination : Methyl 2-methylene-3-phenyl-4-(2-thienylcarbonyl)hex-5-enoate
dc.typeDataset
dc.contributor.departmentChemical Science Program
dc.contributor.departmentHomogeneous Catalysis Laboratory (HCL)
dc.contributor.departmentKAUST Catalysis Center (KCC)
dc.contributor.departmentPhysical Science and Engineering (PSE) Division
kaust.personLee, Richmond
kaust.personTan, Davin
kaust.personHuang, Kuo-Wei
dc.relation.issupplementtoDOI:10.1021/jo400496z
dc.identifier.ccdc909467
display.relations<b> Is Supplement To:</b> <br/> <ul><li><i>[Article]</i> <br/> Tong, G., Zhu, B., Lee, R., Yang, W., Tan, D., Yang, C., … Jiang, Z. (2013). Highly Enantio- and Diastereoselective Allylic Alkylation of Morita–Baylis–Hillman Carbonates with Allyl Ketones. The Journal of Organic Chemistry, 78(10), 5067–5072. doi:10.1021/jo400496z . DOI: <a href="https://doi.org/10.1021/jo400496z">10.1021/jo400496z</a> HANDLE: <a href="http://hdl.handle.net/10754/562767">10754/562767</a></li></ul>


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