Please use this identifier to cite or link to this item: http://repositorio.unifesp.br/handle/11600/29258
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
Authors: Cunha, Rodrigo L. O. R.
Zukerman-Schpector, Julio
Caracelli, I.
Comasseto, Joao V.
Universidade de São Paulo (USP)
Universidade Federal de São Carlos (UFSCar)
Universidade Federal de São Paulo (UNIFESP)
Keywords: tellurium tetrachloride
electrophilic addition
docking
cathepsin B
supramolecular self-assembly
Issue Date: 15-Nov-2006
Publisher: Elsevier B.V.
Citation: Journal of Organometallic Chemistry. Lausanne: Elsevier Science Sa, v. 691, n. 23, p. 4807-4815, 2006.
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.
URI: http://repositorio.unifesp.br/handle/11600/29258
ISSN: 0022-328X
Other Identifiers: http://dx.doi.org/10.1016/j.jorganchem.2006.05.055
Appears in Collections:Em verificação - Geral

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