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DC Field | Value | Language |
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dc.contributor.author | Cunha, Rodrigo L. O. R. | - |
dc.contributor.author | Zukerman-Schpector, Julio | - |
dc.contributor.author | Caracelli, I. | - |
dc.contributor.author | Comasseto, Joao V. | - |
dc.date.accessioned | 2014-05-20T15:21:08Z | - |
dc.date.accessioned | 2016-10-25T17:54:26Z | - |
dc.date.available | 2014-05-20T15:21:08Z | - |
dc.date.available | 2016-10-25T17:54:26Z | - |
dc.date.issued | 2006-11-15 | - |
dc.identifier | http://dx.doi.org/10.1016/j.jorganchem.2006.05.055 | - |
dc.identifier.citation | Journal of Organometallic Chemistry. Lausanne: Elsevier B.V. Sa, v. 691, n. 23, p. 4807-4815, 2006. | - |
dc.identifier.issn | 0022-328X | - |
dc.identifier.uri | http://hdl.handle.net/11449/32305 | - |
dc.identifier.uri | http://acervodigital.unesp.br/handle/11449/32305 | - |
dc.description.abstract | Tellurium tetrachloride adds to alkynes via two pathways: a concerted syn addition, that yields Z-tri- and tetra-substituted alkenes or by an anti addition that yields E-alkenes. The mechanistic aspects of these divergent pathways have been reevaluated at the light of crystallographic data. The molecules, of the title compound, in the crystal, are associated in a helical fashion with a Te...Te pitch of 6.3492(6) angstrom. As it exhibits inhibitory activity for cathepsin B and in order to gain more insight of the inhibition mechanism, a docking study was undertaken providing insight on why organic telluranes are more efficient inhibitors than inorganic ones as AS-101. (c) 2006 Elsevier B.V. All rights reserved. | en |
dc.format.extent | 4807-4815 | - |
dc.language.iso | eng | - |
dc.publisher | Elsevier B.V. | - |
dc.source | Web of Science | - |
dc.subject | tellurium tetrachloride | pt |
dc.subject | electrophilic addition | pt |
dc.subject | docking | pt |
dc.subject | cathepsin B | pt |
dc.subject | supramolecular self-assembly | pt |
dc.title | Revisiting the addition reaction of TeCl4 to alkynes: the crystal structure and docking studies of 1-chloro-2-trichlorotelluro-3-phenyl-propen-2-ol | en |
dc.type | outro | - |
dc.contributor.institution | Universidade de São Paulo (USP) | - |
dc.contributor.institution | Universidade Federal de São Carlos (UFSCar) | - |
dc.contributor.institution | Universidade Estadual Paulista (UNESP) | - |
dc.description.affiliation | Univ São Paulo, Inst Quim, BR-05508900 São Paulo, Brazil | - |
dc.description.affiliation | Univ Fed Sao Carlos, Dept Quim, Lab Cristal Estereodinam & Modelagem Mol, BR-13565905 Sao Carlos, SP, Brazil | - |
dc.description.affiliation | UNESP, Fac Ciências, Dept Fis, Bauru, SP, Brazil | - |
dc.description.affiliationUnesp | UNESP, Fac Ciências, Dept Fis, Bauru, SP, Brazil | - |
dc.identifier.doi | 10.1016/j.jorganchem.2006.05.055 | - |
dc.identifier.wos | WOS:000242304900001 | - |
dc.rights.accessRights | Acesso restrito | - |
dc.relation.ispartof | Journal of Organometallic Chemistry | - |
Appears in Collections: | Artigos, TCCs, Teses e Dissertações da Unesp |
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