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Modular enantioselective access to β-amino amides by Brønsted acid-catalysed multicomponent reactions - Nature Chemistry

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Modular enantioselective access to β-amino amides by Brønsted acid-catalysed multicomponent reactions - Nature Chemistry

β-Amino acids are structural motifs widely found in therapeutic natural products, novel biomimetic polymers and peptidomimetics. As a convergent method, the synthesis of stereoenriched β-amino amides through the asymmetric Mannich reaction requires specialized amide substrates or a metal catalyst for enolate formation. By a redesign of the Ugi reaction, a conceptually different solution to prepare chiral β-amino amides was established using ambiphilic ynamides as two-carbon synthons.

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Modular enantioselective access to β-amino amides by Brønsted acid-catalysed multicomponent reactions - Nature Chemistry

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Modular enantioselective access to β-amino amides by Brønsted acid-catalysed multicomponent reactions - Nature Chemistry

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