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- W2024014561 abstract "Linear depsipeptides have been efficiently cyclised to give cyclodepsipeptide valinomycin analogues via a protocol using activated pentafluorophenyl esters in conjunction with deprotection of a benzylcarbamate by in situ hydrogenolysis. Valinomycins having a 36-membered ring could be obtained in up to 84% yield. Similar cyclisations affording 24- and 48- membered rings also are described." @default.
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- W2024014561 date "1989-01-01" @default.
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- W2024014561 title "Improved methods of synthesis of valinomycins" @default.
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- W2024014561 doi "https://doi.org/10.1016/s0040-4039(00)99557-1" @default.
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