Diastereoselective synthesis of a hydroxamate containing bicyclo-[3.2.0] β-lactam aminal via ruthenium alkene isomerization and Pd(II)-catalyzed oxidative amidation
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference15 articles.
1. The future of the β-lactams
2. Syntheses of Hydroxamic Acid-Containing Bicyclic β-Lactams via Palladium-Catalyzed Oxidative Amidation of Alkenes
3. The azomethine ylide strategy for β-lactam synthesis. Azapenams and 1-azacephams
4. Synthesis of novel fused β-lactams by intramolecular 1,3-dipolar cycloadditions. Part 9. Preparation of the 7-oxo-1,3-diazabicyclo[3.2.0]- heptane-2-carboxylate and 8-oxo-1,3-diazabicyclo[4.2.0]octane-2-carboxylate ring systems
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1. A decade update on synthesis of bicyclic β-lactams and their transformation into synthetically/biologically relevant carbocyclic and heterocyclic moieties;Tetrahedron;2024-11
2. A Neutral PCNHCP Co(I)–Me Pincer Complex as a Catalyst for N-Allylic Isomerization with a Broad Substrate Scope;The Journal of Organic Chemistry;2024-03-23
3. Synthesis of Indoles via Sigmatropic Rearrangements and Olefin Isomerization;Advanced Synthesis & Catalysis;2023-12-28
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