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- W2021159150 abstract "Appropriately protected seryldipeptides which have a relatively acidic proton (H1 of 1) on the α' C can be efficiently converted to β-lactams by reaction with azodicarboxylates and triphenylphosphine. Application of the same reaction conditions to serylamides which lack an acidic α' proton provided dehydropeptides as the major product. Model reactions and potential intermediates which rationalize these results are described." @default.
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- W2021159150 date "1983-01-01" @default.
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- W2021159150 title "The direct chemical conversion of peptides to β-lactams" @default.
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- W2021159150 doi "https://doi.org/10.1016/s0040-4020(01)92149-0" @default.
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