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  4. Photochemical Synthesis of the Bioactive Fragment of Salbutamol and Derivatives in a Self‐Optimizing Flow Chemistry Platform

Photochemical Synthesis of the Bioactive Fragment of Salbutamol and Derivatives in a Self‐Optimizing Flow Chemistry Platform

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Chemistry A European J - 2022 - G rardy - Photochemical Synthesis of the Bioactive Fragment of Salbutamol and Derivatives.pdf

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sword-2022-10-06T15:44:13.original.xml (130 B)
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Author(s)
Gérardy, Romaric
•
Nambiar, Anirudh MK
•
Hart, Travis
•
Mahesh, Prajwal T
•
Jensen, Klavs F
Date Issued
August 2022
Journal
Chemistry – A European Journal
Publisher
Wiley
Citation
Gérardy, Romaric, Nambiar, Anirudh MK, Hart, Travis, Mahesh, Prajwal T and Jensen, Klavs F. 2022. "Photochemical Synthesis of the Bioactive Fragment of Salbutamol and Derivatives in a Self‐Optimizing Flow Chemistry Platform." Chemistry – A European Journal, 28 (43).
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Final published version
Abstract
The implementation of self-optimizing flow reactors has been mostly limited to model reactions or known synthesis routes. In this work, a self-optimizing flow photochemistry platform is used to develop an original synthesis of the bioactive fragment of Salbutamol and derivatives. The key photochemical steps for the construction of the aryl vicinyl amino alcohol moiety consist of a C-C bond forming reaction followed by an unprecedented, high yielding (>80 %), benzylic oxidative cyclization.
MIT Department
Massachusetts Institute of Technology. Department of Chemical Engineering
Terms of Use
Creative Commons Attribution NonCommercial License 4.0
https://creativecommons.org/licenses/by-nc/4.0/
Persistent DSpace Link
https://hdl.handle.net/1721.1/145714
DOI of Published Version
https://doi.org/10.1002/chem.202201385
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