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CC BY-ND-NC 4.0 · Synthesis 2019; 51(01): 203-212
DOI: 10.1055/s-0037-1610391
DOI: 10.1055/s-0037-1610391
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Formation of Complex α-Imino Esters via Multihetero-Cope Rearrangement of α-Keto Ester Derived Nitrones
The project described was supported by Award R35 GM118055 from the National Institute of General Medical Sciences. K.M.K. was supported in part through the Matthew Neely Jackson Undergraduate Research Fellowship (UNC).Weitere Informationen
Publikationsverlauf
Received: 23. Oktober 2018
Accepted: 30. Oktober 2018
Publikationsdatum:
06. Dezember 2018 (online)
This work was carried out in the Department of Chemistry at UNC Chapel Hill, which celebrated its bicentennial in 2018.
Published as part of the 50 Years SYNTHESIS – Golden Anniversary Issue
Abstract
A sequential benzoylation and multihetero-Cope rearrangement of α-keto ester derived nitrones has been developed. The reaction furnishes a diverse array of complex α-imino ester derivatives. The products can be transformed into amino alcohols via LiAlH4 reduction.
Supporting Information
- Supporting information for this article is available online at https://doi.org/10.1055/s-0037-1610391.
- Supporting Information
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