ChemInform
 2016
DOI: 10.1002/chin.201603128
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ChemInform Abstract: Dehydrogenative TEMPO‐Mediated Formation of Unstable Nitrones: Easy Access to N‐Carbamoyl Isoxazolines.

Andrea Gini
1
,
Marwin Segler
2
,
Dominik Kellner
3
et al.

Abstract: Unstable nitrones, formed from the hydroxylamine substrates in the presence of TEMPO, are trapped with alkynes or alkenes to produce the desired isoxazolidines as versatile building blocks of biologically active compounds or natural products (detailed mechanism).

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