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March 13, 2024Synfacts

B(C6F5)3-Catalyzed Diastereoselective Synthesis of Carbocyclic β-Amino Acid (CBAA) Derivatives

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Abstract

Key words carbocyclic β-amino acids - diastereoselective synthesis - 1,5-hydride migration - cyclization - Lewis acid - asymmetric cyclization

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Cite This Study

A 2024 study studied this question.

synapsesocial.com/papers/68e74453b6db6435876bd604 https://doi.org/10.1055/s-0043-1773187

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

1Advances in Transition Metal Catalysis and Organocatalysis Approaches towards Asymmetric Synthesis of β-Amino Acid Derivatives2024 · 8 citations
2A highly enantioselective synthesis of cyclic α-amino acids involving a one-pot, single catalyst, tandem hydrogenation–hydroformylation sequenceElectronic supplementary information (ESI) available: experimental information. See http://www.rsc.org/suppdata/cc/b2/b200374k/Original Research · 2002 · 36 citations
3Lewis Base-Catalyzed β-Amino Acids Synthesis from Trifluoro and Trichloro Acetamide and MBH Carbonates2024 · 1 citations
4Diastereoselective Synthesis of β-Branched α-Amino Acids from β, γ-Unsaturated Amides and Glycine-Derived Imines via Tandem Isomerization-Conjugate AdditionOriginal Research · 2026
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Light‐Driven Epimerization: Diastereoconvergent Synthesis of [ <sup>12</sup> C, <sup>13</sup> C] <i>β</i> <sup>2,3</sup> ‐Amino Acids2026
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