β-Isocupreidine-Catalyzed Asymmetric Baylis−Hillman Reaction of Imines

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Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

1. 1The First Enantioselective and Diastereoselective Catalytic Nitro-Mannich Reaction: A New Entry to Chiral Vicinal Diamines2001 · 94 citations
2. 2Active Site Design in a Chemzyme: Development of a Highly Asymmetric and Remarkably Temperature-Independent Catalyst for the Imino Aldol Reaction This work was supported by a grant from UOP Company. We would like to thank Thomas Malloy, Timothy Brandvold and Beth McCulloch for stimulating discussions.2001 · 75 citations
3. 3Active Site Design in a Chemzyme: Development of a Highly Asymmetric and Remarkably Temperature-Independent Catalyst for the Imino Aldol Reaction2001 · 96 citations
4. 4Phosphinamides: a new class of amino protecting groups in peptide synthesis1984 · 59 citations
5. 5Catalytic, Asymmetric Baylis–Hillman Reaction of Imines with Methyl Vinyl Ketone and Methyl Acrylate2002 · 232 citations