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Rhodium-catalysed syn-carboamination of alkenes via a transient directing group

Author

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  • Tiffany Piou

    (Colorado State University)

  • Tomislav Rovis

    (Colorado State University)

Abstract

Chemical methods for adding carbon-based or nitrogen-based functional groups to alkenes are well established, but strategies for adding both to the same double bond have limitations; here, a method for the carboamination of alkenes at the same double bond is described.

Suggested Citation

  • Tiffany Piou & Tomislav Rovis, 2015. "Rhodium-catalysed syn-carboamination of alkenes via a transient directing group," Nature, Nature, vol. 527(7576), pages 86-90, November.
    • Handle: RePEc:nat:nature:v:527:y:2015:i:7576:d:10.1038_nature15691
    DOI: 10.1038/nature15691
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    Cited by:

    1. Souvik Ghosal & Ankita Das & Debojyoti Roy & Jyotishman Dasgupta, 2024. "Tuning light-driven oxidation of styrene inside water-soluble nanocages," Nature Communications, Nature, vol. 15(1), pages 1-16, December.
    2. Yang Zheng & Wen-Yun Zhang & Qing Gu & Chao Zheng & Shu-Li You, 2023. "Cobalt(III)-catalyzed asymmetric ring-opening of 7-oxabenzonorbornadienes via indole C–H functionalization," Nature Communications, Nature, vol. 14(1), pages 1-9, December.

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