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Asymmetric reduction of 4-Bromo-Acetophenone using whole cells
Asymmetric reduction of 4-Bromo-Acetophenone using whole cells
Ribeiro, Joyce Benzaquem; Lopes, Raquel de Oliveira; Vechia, Luciana Dalla; Ramos, Aline de Souza; Leite, Selma Gomes Ferreira; Souza, Rodrigo Octavio Mendonça Alves de
Abstract:
Biocatalysis has become an increasingly valuable tool for synthetic chemists. Chiral alcohols with additional functional groups are very important intermediates in the synthesis of enantiomerically pure pharmaceuticals and other important chemicals. Chiral phenylethanols (R or S) are an interesting compounds with a number of potential applications, particularly in the drug industry. These alcohols are used as building blocks for the synthesis of bioactive compounds such as pharmaceuticals, agrochemicals and natural products. In this work, we report the use of 14 microorganisms for the asymmetric reduction of 4-Br-acetophenone.
Biocatalysis has become an increasingly valuable tool for synthetic chemists. Chiral alcohols with additional functional groups are very important intermediates in the synthesis of enantiomerically pure pharmaceuticals and other important chemicals. Chiral phenylethanols (R or S) are an interesting compounds with a number of potential applications, particularly in the drug industry. These alcohols are used as building blocks for the synthesis of bioactive compounds such as pharmaceuticals, agrochemicals and natural products. In this work, we report the use of 14 microorganisms for the asymmetric reduction of 4-Br-acetophenone.
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DOI: 10.5151/chempro-14bmos-R0206-1
Referências bibliográficas
- [1] 1 Kurbanoglu, E.B., Zilbeyaz, K., Ozdal, M., Taskin, M., Kurbanoglu, N.I. Bioresource Technology 2010, 101, 3825–3829
- [2] 2 Zilbeyaz, K., Kurbanoglu, E.B. Bioresource Technology, 2008, 99, 1549–1552
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Ribeiro, Joyce Benzaquem; Lopes, Raquel de Oliveira; Vechia, Luciana Dalla; Ramos, Aline de Souza; Leite, Selma Gomes Ferreira; Souza, Rodrigo Octavio Mendonça Alves de; "Asymmetric reduction of 4-Bromo-Acetophenone using whole cells", p-206-206.
In: In Blucher Chemistry Proceedings, São Paulo, v. 1, n. 1, Setembro.2013.
São Paulo: Blucher,
2013.
ISSN 23184043,
DOI 10.5151/chempro-14bmos-R0206-1
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TY - CONF T1 - Asymmetric reduction of 4-Bromo-Acetophenone using whole cells JO - Blucher Chemistry Proceedings VL - 1 IS - 1 SP - 206 EP - 206 PY - 2013 T2 - Brazilian Meeting on Organic Synthesis 2011 AU - , , , , , SN - 23184043 DO - http://dx.doi.org/10.5151/chempro-14bmos-R0206-1 UR - www.proceedings.blucher.com.br/article-details/asymmetric-reduction-of-4-bromo-acetophenone-using-whole-cells-8058 KW - ER -
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@article{Ribeiro20144,
title="Asymmetric reduction of 4-Bromo-Acetophenone using whole cells",
journal="Blucher Chemistry Proceedings",
volume="1",
number="1",
pages="206 - 206",
year="2013",
note="",
issn="23184043",
doi="http://dx.doi.org/10.5151/chempro-14bmos-R0206-1",
url="www.proceedings.blucher.com.br/article-details/asymmetric-reduction-of-4-bromo-acetophenone-using-whole-cells-8058",
author="Joyce Benzaquem Ribeiro", "Raquel de Oliveira Lopes", "Luciana Dalla Vechia", "Aline de Souza Ramos", "Selma Gomes Ferreira Leite", "Rodrigo Octavio Mendonça Alves de Souza",
keywords="",
}
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Joyce Benzaquem Ribeiro, Raquel de Oliveira Lopes, Luciana Dalla Vechia, Aline de Souza Ramos, Selma Gomes Ferreira Leite, Rodrigo Octavio Mendonça Alves de Souza, Asymmetric reduction of 4-Bromo-Acetophenone using whole cells, Blucher Chemistry Proceedings, Volume 1, 2013, Pages 206-206, ISSN 23184043, http://dx.doi.org/10.5151/chempro-14bmos-R0206-1 (www.proceedings.blucher.com.br/article-details/asymmetric-reduction-of-4-bromo-acetophenone-using-whole-cells-8058) Palavras-chave:: ;