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Ring opening of photogenerated azetidinols as a strategy for the synthesis of aminodioxolanes

α-Aminoacetophenones are identified as promising building blocks for the synthesis of highly substituted dioxolanes. The presented strategy is founded on the build and release of molecular strain and achieves a formal transposition of a methyl group. During light irradiation, 3-phenylazetidinols are...

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Bibliografski detalji
Glavni autori: Henning Maag, Daniel J. Lemcke, Johannes M. Wahl
Format: Artigo
Jezik:Inglês
Izdano: Beilstein-Institut 2024-07-01
Serija:Beilstein Journal of Organic Chemistry
Teme:
Online pristup:https://doi.org/10.3762/bjoc.20.148
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