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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/32305
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
Author(s): 
Institution: 
  • Universidade de São Paulo (USP)
  • Universidade Federal de São Carlos (UFSCar)
  • Universidade Estadual Paulista (UNESP)
ISSN: 
0022-328X
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.
Issue Date: 
15-Nov-2006
Citation: 
Journal of Organometallic Chemistry. Lausanne: Elsevier B.V. Sa, v. 691, n. 23, p. 4807-4815, 2006.
Time Duration: 
4807-4815
Publisher: 
Elsevier B.V.
Keywords: 
  • tellurium tetrachloride
  • electrophilic addition
  • docking
  • cathepsin B
  • supramolecular self-assembly
Source: 
http://dx.doi.org/10.1016/j.jorganchem.2006.05.055
URI: 
Access Rights: 
Acesso restrito
Type: 
outro
Source:
http://repositorio.unesp.br/handle/11449/32305
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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