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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
- Universidade de São Paulo (USP)
- Universidade Federal de São Carlos (UFSCar)
- Universidade Estadual Paulista (UNESP)
- 0022-328X
- 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.
- 15-Nov-2006
- Journal of Organometallic Chemistry. Lausanne: Elsevier B.V. Sa, v. 691, n. 23, p. 4807-4815, 2006.
- 4807-4815
- Elsevier B.V.
- tellurium tetrachloride
- electrophilic addition
- docking
- cathepsin B
- supramolecular self-assembly
- http://dx.doi.org/10.1016/j.jorganchem.2006.05.055
- Acesso restrito
- outro
- http://repositorio.unesp.br/handle/11449/32305
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