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http://acervodigital.unesp.br/handle/11449/26344
- Title:
- Albendazole sulfoxide enantiomers: Preparative chiral separation and absolute stereochemistry
- Universidade Federal de São Carlos (UFSCar)
- Universidade Estadual Paulista (UNESP)
- BioTools Inc
- Syracuse Univ
- Universidade Estadual de Campinas (UNICAMP)
- 0021-9673
- Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
- Center for Scientific Computing (NCC/GridUNESP) of the São Paulo State University (UNESP)
- Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)
- FAPESP: 09/18515-1
- FAPESP: 08/58658-3
- FAPESP: 09/17138-0
- FAPESP: 07/02872-4
- The enantiomeric separation of albendazole sulfoxide was carried out by simulated moving bed chromatography with variable zones (VARICOL). An overall recovery of 97% was achieved and enantiomeric ratios of 99.5% for raffinate and 99.0% for extract were attained. A total of 880 mg of (+)-albendazol sulfoxide and 930 mg of its antipode were collected after 55 cycles or 11 h of process, resulting in a mass rate of 2 g/day. Furthermore the absolute configuration of the enantiopure compounds was determined for the first time by vibrational circular dichroism (VCD) with the aid of theoretical calculations as (-)-(S) and (+)-(R)-albendazole sulfoxide. (C) 2012 Elsevier B.V. All rights reserved.
- 23-Mar-2012
- Journal of Chromatography A. Amsterdam: Elsevier B.V., v. 1230, p. 61-65, 2012.
- 61-65
- Elsevier B.V.
- Albendazole sulfoxide
- Simulated moving bed chromatography
- VARICOL process
- Multimilligram enantiomeric separation
- Vibrational circular dichroism
- Absolute configuration
- http://dx.doi.org/10.1016/j.chroma.2012.01.070
- Acesso restrito
- outro
- http://repositorio.unesp.br/handle/11449/26344
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