Answers are grounded in this paper and cite their sources.
The synthesis of ( S )- N -Boc-bis(4-fluorophenyl)alanine, an intermediate in the synthesis of denagliptin, is described from the synthesis of a 12 g proof of principle sample to a >900 kg cGMP manufacturing campaign. The chiral centre was established by the asymmetric hydrogenation of the sterically crowded precursor, ethyl 2-acetamido-3,3-bis(4-fluorophenyl)acrylate. The ability to isolate the various intermediates in a physical form that would readily allow filtration, washing, and ultimately purification underpinned the successful manufacturing campaign.
No takes yet. Share an insight, caveat, or question.
Appell et al. (2012) studied this question.
Synapse has enriched 10 related papers. Consider them for comparative context: