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- W4254800549 endingPage "5863" @default.
- W4254800549 startingPage "5859" @default.
- W4254800549 abstract "Abstract Natural products of polyketide origin, in particular small‐sized lactones often possess a very broad range of impressive biological activities. An efficient way to demonstrate the concise access to six‐membered lactones was emphasized as part of a stereodivergent and protecting‐group‐free synthesis of all three representatives of the helicascolide family. This strategy features an atom‐economical and highly diastereoselective rhodium‐catalyzed “head‐to‐tail” lactonization by an intramolecular addition of ω‐allenyl‐substituted carboxylic acids to terminal allenes, including the selective construction of a new stereocenter in the newly formed core structures. The excellent selectivities with which the helicascolide precursors were obtained are remarkable, thus resulting in an expeditious and highly efficient natural product synthesis." @default.
- W4254800549 created "2022-05-12" @default.
- W4254800549 creator A5062379384 @default.
- W4254800549 creator A5063672065 @default.
- W4254800549 creator A5067624195 @default.
- W4254800549 creator A5070891497 @default.
- W4254800549 date "2016-04-04" @default.
- W4254800549 modified "2023-10-14" @default.
- W4254800549 title "Stereodivergent and Protecting-Group-Free Synthesis of the Helicascolide Family: A Rhodium-Catalyzed Atom-Economical Lactonization Strategy" @default.
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