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- W4245573111 endingPage "15754" @default.
- W4245573111 startingPage "15750" @default.
- W4245573111 abstract "Natural products of polyketide origin with a high level of symmetry, in particular C2-symmetric diolides as a special macrolactone-based product class, often possess a broad spectrum of biological activity. An efficient route to this important structural motif was developed as part of a concise and highly convergent synthesis of clavosolide A. This strategy features an atom-economic “head-to-tail” dimerization by the stereoselective rhodium-catalyzed addition of carboxylic acids to terminal allenes with the simultaneous construction of two new stereocenters. The excellent efficiency and selectivity with which the C2-symmetric core structures were obtained are remarkable considering the outcome under classical dimerization conditions. Furthermore, this approach facilitates late-stage modification and provides ready access to potential new lead structures." @default.
- W4245573111 created "2022-05-12" @default.
- W4245573111 creator A5067624195 @default.
- W4245573111 creator A5070891497 @default.
- W4245573111 date "2015-11-10" @default.
- W4245573111 modified "2023-09-27" @default.
- W4245573111 title "Atom-Economical Dimerization Strategy by the Rhodium-Catalyzed Addition of Carboxylic Acids to Allenes: Protecting-Group-Free Synthesis of Clavosolide A and Late-Stage Modification" @default.
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