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(Reference retrieved automatically from Web of Science through information on FAPESP grant and its corresponding number as mentioned in the publication by the authors.)

Novel deoxy-selenylconduritols: chemoenzymatic synthesis and biological evaluation

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Author(s):
Bellomo, Ana [1] ; Bertucci, Ana [2] ; Stefani, Helio [3, 4] ; Vazquez, Alvaro [2] ; Gonzalez, David [1]
Total Authors: 5
Affiliation:
[1] Univ Republica, UdelaR, Fac Quim, Lab Sintesis Organ, Montevideo - Uruguay
[2] Univ Republica, UdelaR, Fac Quim, Lab Farmacognosia & Prod Nat, Montevideo - Uruguay
[3] Univ Fed Sao Paulo, Dept Biofis, Sao Paulo - Brazil
[4] Univ Sao Paulo, Fac Ciencias Farmaceut, Dept Farm, Sao Paulo - Brazil
Total Affiliations: 4
Document type: Journal article
Source: TETRAHEDRON-ASYMMETRY; v. 20, n. 23, p. 2673-2676, DEC 11 2009.
Web of Science Citations: 10
Abstract

The first synthesis of two selenyldeoxycyclitols (4-bromo-2-phenylselenyl conduritol F and 6-phenylselenylconduritol F) is reported via a chemoenzymatic enantioselective route. The key step of the synthesis is the selenolysis of a vinyl epoxide. The new compounds were evaluated for their capacity to inhibit the growth of different microorganisms using a modification of the agar diffusion technique with thin layer chromatography plates as support. (C) 2009 Elsevier Ltd. All rights reserved. (AU)