Base-Promoted C→N Carbonyl Shift Enables One-Step Access to aza-β-Lactams from α-Heteroaryl-α-amino Esters

-substituents. Isolation and productive re-entry of a carbamate intermediate support a reversible manifold preceding migration and rationalize racemic product formation.

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Publication Details

Journal
Organic Letters
Published
2026-05-11
DOI
https://doi.org/10.1021/acs.orglett.6c01451
Primary Topic
Synthesis of β-Lactam Compounds
Type
article
Field-Weighted Citation Impact
0.00

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article

Base-Promoted C→N Carbonyl Shift Enables One-Step Access to aza-β-Lactams from α-Heteroaryl-α-amino Esters

Jozef Kristek, Jiří Pospíšil, Nikola Šťastná
Organic Letters
Synthesis of β-Lactam Compounds
article

Base-Promoted C→N Carbonyl Shift Enables One-Step Access to aza-β-Lactams from α-Heteroaryl-α-amino Esters

Jozef Kristek, Jiří Pospíšil, Nikola Šťastná
article en

Abstract

-substituents. Isolation and productive re-entry of a carbamate intermediate support a reversible manifold preceding migration and rationalize racemic product formation.

Organic Letters
Czech Academy of Sciences, Institute of Experimental Botany (CZ), Palacký University Olomouc (CZ)
Univerzita Palackého v Olomouci, European Regional Development Fund
Reduced inequalities
Openalex Percentile: Top 10%
Synthesis of β-Lactam Compounds
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