Bioreduction of Morita-Baylis-Hillman Adducts and Derivatives: A New Approach to Asymmetric Chemo-enzymatic Synthesis of Fragrances

Bioreduction of Morita-Baylis-Hillman Adducts and Derivatives: A New Approach to Asymmetric Chemo-enzymatic Synthesis of Fragrances

Ferreira, Bruno R. Vilachã; Zampieri, Dávila S.; Moran, Paulo J. S.; Rodrigues, José A. R.; Coelho, Fernando

Abstract:

The synthesis of optically active compounds is a highly challenging task for organic chemists, especially if targeted final products possess remarkable applications for the fine chemical industrial sector. It has been extensively demonstrated along recent years that Biocatalysis offers ecological, economic, scalable and straightforward methods for the production of fine chemical with high enantiomeric excess. For all of that, we have focused our attention in the production of chiral fragrances.

The synthesis of optically active compounds is a highly challenging task for organic chemists, especially if targeted final products possess remarkable applications for the fine chemical industrial sector. It has been extensively demonstrated along recent years that Biocatalysis offers ecological, economic, scalable and straightforward methods for the production of fine chemical with high enantiomeric excess. For all of that, we have focused our attention in the production of chiral fragrances.

Palavras-chave:

DOI: 10.5151/chempro-14bmos-R0117-1

Referências bibliográficas

• [1] 1 Vieira, G. A. B. et al. Tetrahedron:Asymm. 2009, 20, 214.
• [2] 2 Ferreira, B. R. V., PhD Thesis, State University Campinas, Brazil, 2010.
• [3] 3 Zampieri, D. S., PhD Thesis, State University Campinas, Brazil, 2011.

Como citar:

Ferreira, Bruno R. Vilachã; Zampieri, Dávila S.; Moran, Paulo J. S.; Rodrigues, José A. R.; Coelho, Fernando; "Bioreduction of Morita-Baylis-Hillman Adducts and Derivatives: A New Approach to Asymmetric Chemo-enzymatic Synthesis of Fragrances", p-117-117. In: In Blucher Chemistry Proceedings, São Paulo, v. 1, n. 1, Setembro.2013. São Paulo: Blucher, 2013.
ISSN 23184043, DOI 10.5151/chempro-14bmos-R0117-1