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- W1999463545 abstract "Abstract With antibiotic resistance on the rise, the need for new medicinal scaffolds is needed. The synthesis of an aminal bicyclic β-lactam core is described. The key synthetic step is Pd(II)-catalyzed oxidative amidation. The product is a single diastereomer, confirmed by X-ray crystallography." @default.
- W1999463545 created "2016-06-24" @default.
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- W1999463545 date "2015-06-01" @default.
- W1999463545 modified "2023-09-27" @default.
- W1999463545 title "Diastereoselective synthesis of a hydroxamate containing bicyclo-[3.2.0] β-lactam aminal via ruthenium alkene isomerization and Pd(II)-catalyzed oxidative amidation" @default.
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- W1999463545 doi "https://doi.org/10.1016/j.tetlet.2014.12.072" @default.
- W1999463545 hasPublicationYear "2015" @default.
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