Synthesis of 2,5‐disubstituted pyrrolidine alkaloids via A one‐pot cascade using transaminase and reductive aminase biocatalysts
Bruna Z. Costa, James L. Galman, Iustina Slabu, Scott P. France, Anita J. Marsaioli, Nicholas J. Turner
ARTIGO
Inglês
A multi‐enzymatic cascade process involving transaminases (TAs) and reductive aminases (RedAms) to produce enantiomerically pure 2,5‐disubstituted pyrrolidine alkaloids from their respective 1,4‐diketones is reported. Several TAs were screened and the bes
CONSELHO NACIONAL DE DESENVOLVIMENTO CIENTÍFICO E TECNOLÓGICO - CNPQ
307885/2013-5
FUNDAÇÃO DE AMPARO À PESQUISA DO ESTADO DE SÃO PAULO - FAPESP
2014/50249-8; 2014/22967-3; 2015/22513-5
Fechado
Synthesis of 2,5‐disubstituted pyrrolidine alkaloids via A one‐pot cascade using transaminase and reductive aminase biocatalysts
Bruna Z. Costa, James L. Galman, Iustina Slabu, Scott P. France, Anita J. Marsaioli, Nicholas J. Turner
Synthesis of 2,5‐disubstituted pyrrolidine alkaloids via A one‐pot cascade using transaminase and reductive aminase biocatalysts
Bruna Z. Costa, James L. Galman, Iustina Slabu, Scott P. France, Anita J. Marsaioli, Nicholas J. Turner
Fontes
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Chemcatchem (Fonte avulsa) |