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Synthesis of the oxazolidinone fragment of thelepamide. | LitMetric

Synthesis of the oxazolidinone fragment of thelepamide.

Nat Prod Res

Graduate School of Environmental and Life Science, Okayama University, Okayama, Japan.

Published: April 2022

AI Article Synopsis

Article Abstract

Thelepamide, an unique ketide-amino acid isolated from a marine annelid worm , has a unique oxazolidinone ring derived from cysteine, glycine and valine. Rareness in nature as well as promising bioactive possibility make the oxazolidinone ring an attractive synthetic target. The hydroxy oxazolidinone fragment of thelepamide was prepared by acid-catalysed ,-acetal formation between a ketoamide and formaldehyde. Lactone-carbonyl selective isopropyl addition to an oxazilidine-dione under Grignard conditions also forms the target compound.

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http://dx.doi.org/10.1080/14786419.2020.1809398DOI Listing

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